RAD54L (RAD54 like) - Rat Genome Database

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Gene: RAD54L (RAD54 like) Homo sapiens
Analyze
Symbol: RAD54L
Name: RAD54 like
RGD ID: 1321600
HGNC Page HGNC:9826
Description: Enables ATP-dependent DNA/DNA annealing activity. Predicted to be involved in double-strand break repair via synthesis-dependent strand annealing and reciprocal meiotic recombination. Predicted to act upstream of or within several processes, including determination of adult lifespan; double-strand break repair via homologous recombination; and response to ionizing radiation. Located in nucleoplasm. Part of protein-containing complex. Implicated in breast cancer; disease of cellular proliferation; non-Hodgkin lymphoma; and pancreatic cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DNA repair and recombination protein RAD54-like; hHR54; HR54; hRAD54; RAD54 homolog; RAD54 like (S. cerevisiae); RAD54-like (S. cerevisiae); RAD54A
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38146,247,688 - 46,278,473 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl146,246,461 - 46,278,480 (+)EnsemblGRCh38hg38GRCh38
GRCh37146,713,360 - 46,744,145 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36146,486,004 - 46,516,732 (+)NCBINCBI36Build 36hg18NCBI36
Build 34146,425,436 - 46,456,165NCBI
Celera145,000,746 - 45,031,525 (+)NCBICelera
Cytogenetic Map1p34.1NCBI
HuRef144,829,132 - 44,859,988 (+)NCBIHuRef
CHM1_1146,830,372 - 46,861,163 (+)NCBICHM1_1
T2T-CHM13v2.0146,124,906 - 46,155,694 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,4-diaminotoluene  (ISO)
3-methylcholanthrene  (ISO)
4-hydroxynon-2-enal  (ISO)
acetamide  (ISO)
aflatoxin B1  (EXP)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP)
AM-251  (EXP)
antimycin A  (EXP)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[e]pyrene  (EXP)
Biflorin  (EXP)
bis(2-chloroethyl) sulfide  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
cadmium dichloride  (EXP)
calcitriol  (EXP)
cannabidiol  (EXP)
carbon nanotube  (ISO)
chlorpyrifos  (ISO)
chromium(6+)  (ISO)
cisplatin  (ISO)
copper atom  (EXP)
copper(0)  (EXP)
copper(II) sulfate  (EXP)
coumestrol  (EXP)
cyclophosphamide  (ISO)
DDE  (EXP)
dibutyl phthalate  (ISO)
dioxygen  (EXP)
doxorubicin  (ISO)
Enterolactone  (EXP)
epoxiconazole  (ISO)
etoposide  (EXP)
geraniol  (EXP)
imiquimod  (ISO)
lead(0)  (EXP)
lidocaine  (ISO)
MeIQx  (EXP)
methamphetamine  (ISO)
methapyrilene  (EXP)
N(4)-hydroxycytidine  (ISO)
N-acetyl-L-cysteine  (EXP)
niclosamide  (EXP)
oxaliplatin  (ISO)
ozone  (ISO)
paracetamol  (EXP,ISO)
perfluorooctanoic acid  (EXP)
phorbol 13-acetate 12-myristate  (EXP)
propanal  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
silicon dioxide  (EXP,ISO)
sodium arsenite  (EXP)
succimer  (ISO)
sunitinib  (EXP)
testosterone  (EXP)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
thioacetamide  (ISO)
topotecan  (ISO)
trimellitic anhydride  (ISO)
triptonide  (ISO)
troglitazone  (EXP)
trovafloxacin  (ISO)
tunicamycin  (EXP)
vinclozolin  (ISO)
vincristine  (EXP)
zaragozic acid A  (ISO)
zinc atom  (EXP)
zinc(0)  (EXP)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Significant effect of homologous recombination DNA repair gene polymorphisms on pancreatic cancer survival. Li D, etal., Cancer Res. 2006 Mar 15;66(6):3323-30.
3. Mutations in the RAD54 recombination gene in primary cancers. Matsuda M, etal., Oncogene. 1999 Jun 3;18(22):3427-30.
4. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
5. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
6. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
8. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
Additional References at PubMed
PMID:8805304   PMID:8889548   PMID:9192813   PMID:9321665   PMID:9774452   PMID:10449612   PMID:10640146   PMID:11289143   PMID:11459989   PMID:11799067   PMID:12205100   PMID:12477932  
PMID:12614485   PMID:15489334   PMID:15782160   PMID:15806108   PMID:15975611   PMID:16344560   PMID:16520463   PMID:16710414   PMID:16862129   PMID:16990250   PMID:17054727   PMID:17417655  
PMID:17545145   PMID:17660833   PMID:18203022   PMID:18270339   PMID:18617519   PMID:18676680   PMID:19147782   PMID:19170196   PMID:19573080   PMID:19625176   PMID:19692168   PMID:19773279  
PMID:20301425   PMID:20496165   PMID:20522537   PMID:20610542   PMID:20813000   PMID:21873635   PMID:22153077   PMID:22705370   PMID:24163370   PMID:24798879   PMID:25416956   PMID:25765654  
PMID:25965574   PMID:26496610   PMID:28514442   PMID:29295984   PMID:32333827   PMID:32694731   PMID:33261027   PMID:33637726   PMID:33961781   PMID:34079088   PMID:34169999   PMID:35559673  
PMID:36071250   PMID:36454390   PMID:36724073   PMID:37499664   PMID:38593124  


Genomics

Comparative Map Data
RAD54L
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38146,247,688 - 46,278,473 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl146,246,461 - 46,278,480 (+)EnsemblGRCh38hg38GRCh38
GRCh37146,713,360 - 46,744,145 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36146,486,004 - 46,516,732 (+)NCBINCBI36Build 36hg18NCBI36
Build 34146,425,436 - 46,456,165NCBI
Celera145,000,746 - 45,031,525 (+)NCBICelera
Cytogenetic Map1p34.1NCBI
HuRef144,829,132 - 44,859,988 (+)NCBIHuRef
CHM1_1146,830,372 - 46,861,163 (+)NCBICHM1_1
T2T-CHM13v2.0146,124,906 - 46,155,694 (+)NCBIT2T-CHM13v2.0
Rad54l
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394115,951,458 - 115,980,875 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4115,951,461 - 115,980,887 (-)EnsemblGRCm39 Ensembl
GRCm384116,094,261 - 116,123,700 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4116,094,264 - 116,123,690 (-)EnsemblGRCm38mm10GRCm38
MGSCv374115,769,560 - 115,796,295 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364115,594,907 - 115,621,591 (-)NCBIMGSCv36mm8
Celera4114,835,105 - 114,861,841 (-)NCBICelera
Cytogenetic Map4D1NCBI
cM Map453.1NCBI
Rad54l
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85134,812,158 - 134,841,821 (-)NCBIGRCr8
mRatBN7.25129,575,431 - 129,605,100 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5129,575,378 - 129,605,070 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5132,191,515 - 132,221,172 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05133,946,399 - 133,975,757 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05133,968,540 - 133,998,199 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05134,948,511 - 134,978,125 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5134,948,512 - 134,978,125 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05138,732,242 - 138,762,035 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.15136,209,780 - 136,239,533 (+)NCBI
Celera5128,105,213 - 128,134,839 (-)NCBICelera
Cytogenetic Map5q35NCBI
Rad54l
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495546411,996,512 - 12,033,490 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495546411,996,512 - 12,033,525 (-)NCBIChiLan1.0ChiLan1.0
RAD54L
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21180,529,512 - 180,575,654 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11179,671,110 - 179,717,249 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0145,549,586 - 45,581,711 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1146,905,598 - 46,936,532 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl146,905,598 - 46,936,259 (+)Ensemblpanpan1.1panPan2
RAD54L
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11514,111,168 - 14,139,819 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1514,111,157 - 14,139,301 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1514,234,015 - 14,262,340 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01514,264,072 - 14,292,635 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1514,264,092 - 14,292,579 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11514,065,329 - 14,093,894 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01514,133,819 - 14,162,383 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01514,203,309 - 14,231,866 (-)NCBIUU_Cfam_GSD_1.0
Rad54l
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505861,455,182 - 61,491,646 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647427,280,573 - 27,316,428 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647427,276,570 - 27,316,427 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RAD54L
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6165,152,978 - 165,184,776 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16165,156,833 - 165,184,641 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.26152,636,270 - 152,664,106 (-)NCBISscrofa10.2Sscrofa10.2susScr3
RAD54L
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12086,510,616 - 86,542,426 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2086,507,248 - 86,542,663 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603330,444,520 - 30,476,524 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Rad54l
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249062,165,780 - 2,193,764 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249062,164,711 - 2,194,262 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in RAD54L
990 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_003579.4(RAD54L):c.188C>A (p.Pro63His) single nucleotide variant Colon adenocarcinoma [RCV000006568] Chr1:46250097 [GRCh38]
Chr1:46715769 [GRCh37]
Chr1:1p34.1
pathogenic|other
NM_003579.4(RAD54L):c.1331T>A (p.Val444Glu) single nucleotide variant Non-Hodgkin lymphoma [RCV000006569] Chr1:46272758 [GRCh38]
Chr1:46738430 [GRCh37]
Chr1:1p34.1
pathogenic|other
NM_003579.4(RAD54L):c.973G>A (p.Gly325Arg) single nucleotide variant Breast ductal adenocarcinoma [RCV000006570] Chr1:46267540 [GRCh38]
Chr1:46733212 [GRCh37]
Chr1:1p34.1
pathogenic
GRCh38/hg38 1p34.3-33(chr1:39479787-47688131)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051817]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051817]|See cases [RCV000051817] Chr1:39479787..47688131 [GRCh38]
Chr1:39945459..48153803 [GRCh37]
Chr1:39718046..47926390 [NCBI36]
Chr1:1p34.3-33
pathogenic
NM_003579.4(RAD54L):c.1033G>T (p.Gly345Cys) single nucleotide variant Inborn genetic diseases [RCV000190710] Chr1:46267600 [GRCh38]
Chr1:46733272 [GRCh37]
Chr1:1p34.1
pathogenic|likely pathogenic
NM_003579.4(RAD54L):c.1624C>T (p.Arg542Cys) single nucleotide variant Inborn genetic diseases [RCV000210737] Chr1:46274151 [GRCh38]
Chr1:46739823 [GRCh37]
Chr1:1p34.1
likely pathogenic
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12
likely benign
NM_003579.4(RAD54L):c.1094G>A (p.Arg365Gln) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV001374572] Chr1:46270710 [GRCh38]
Chr1:46736382 [GRCh37]
Chr1:1p34.1
uncertain significance
GRCh37/hg19 1p34.1(chr1:46078097-46725770)x3 copy number gain See cases [RCV000448110] Chr1:46078097..46725770 [GRCh37]
Chr1:1p34.1
uncertain significance
GRCh37/hg19 1p34.1-32.3(chr1:45303358-52157856)x1 copy number loss See cases [RCV000448358] Chr1:45303358..52157856 [GRCh37]
Chr1:1p34.1-32.3
likely pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p34.1-33(chr1:46541307-47088882)x3 copy number gain See cases [RCV000511609] Chr1:46541307..47088882 [GRCh37]
Chr1:1p34.1-33
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_003579.4(RAD54L):c.712A>C (p.Ile238Leu) single nucleotide variant not specified [RCV004327929] Chr1:46260961 [GRCh38]
Chr1:46726633 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1881T>C (p.Ile627=) single nucleotide variant not specified [RCV004327930] Chr1:46277828 [GRCh38]
Chr1:46743500 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2142G>C (p.Gly714=) single nucleotide variant not specified [RCV004327939] Chr1:46278180 [GRCh38]
Chr1:46743852 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.843T>C (p.His281=) single nucleotide variant not specified [RCV004327940] Chr1:46261337 [GRCh38]
Chr1:46727009 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1772T>C (p.Phe591Ser) single nucleotide variant not specified [RCV004330306] Chr1:46274620 [GRCh38]
Chr1:46740292 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.148C>G (p.Pro50Ala) single nucleotide variant not specified [RCV004330307] Chr1:46250057 [GRCh38]
Chr1:46715729 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1526G>T (p.Arg509Leu) single nucleotide variant not specified [RCV004330319] Chr1:46273663 [GRCh38]
Chr1:46739335 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.286C>G (p.Arg96Gly) single nucleotide variant not specified [RCV004330321] Chr1:46259978 [GRCh38]
Chr1:46725650 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.275C>T (p.Pro92Leu) single nucleotide variant not specified [RCV004330322] Chr1:46259967 [GRCh38]
Chr1:46725639 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.33C>T (p.Ala11=) single nucleotide variant not specified [RCV004330325] Chr1:46248541 [GRCh38]
Chr1:46714213 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.767A>G (p.Glu256Gly) single nucleotide variant not specified [RCV004326074] Chr1:46261261 [GRCh38]
Chr1:46726933 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1671A>G (p.Glu557=) single nucleotide variant not specified [RCV004326075] Chr1:46274198 [GRCh38]
Chr1:46739870 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.13T>C (p.Leu5=) single nucleotide variant not specified [RCV004327926] Chr1:46248521 [GRCh38]
Chr1:46714193 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2231G>A (p.Arg744Gln) single nucleotide variant not specified [RCV004327927] Chr1:46278269 [GRCh38]
Chr1:46743941 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2079C>T (p.Pro693=) single nucleotide variant not specified [RCV004327928] Chr1:46278117 [GRCh38]
Chr1:46743789 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.322G>T (p.Ala108Ser) single nucleotide variant not specified [RCV004327936] Chr1:46260014 [GRCh38]
Chr1:46725686 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1529G>A (p.Ser510Asn) single nucleotide variant not specified [RCV004327938] Chr1:46273666 [GRCh38]
Chr1:46739338 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1791A>T (p.Pro597=) single nucleotide variant not specified [RCV004327942] Chr1:46274639 [GRCh38]
Chr1:46740311 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1134G>A (p.Glu378=) single nucleotide variant not specified [RCV004327943] Chr1:46270750 [GRCh38]
Chr1:46736422 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.610A>G (p.Ser204Gly) single nucleotide variant not specified [RCV004330308] Chr1:46260859 [GRCh38]
Chr1:46726531 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1756A>C (p.Asn586His) single nucleotide variant not specified [RCV004330314] Chr1:46274604 [GRCh38]
Chr1:46740276 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2102C>T (p.Ser701Leu) single nucleotide variant not specified [RCV004330316] Chr1:46278140 [GRCh38]
Chr1:46743812 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.893G>C (p.Gly298Ala) single nucleotide variant not specified [RCV004330320] Chr1:46267460 [GRCh38]
Chr1:46733132 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1065G>A (p.Lys355=) single nucleotide variant not specified [RCV004330327] Chr1:46270681 [GRCh38]
Chr1:46736353 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1980G>A (p.Glu660=) single nucleotide variant not specified [RCV004330328] Chr1:46277927 [GRCh38]
Chr1:46743599 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1026T>G (p.Val342=) single nucleotide variant not specified [RCV004330329] Chr1:46267593 [GRCh38]
Chr1:46733265 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1192G>A (p.Asp398Asn) single nucleotide variant not specified [RCV004330330] Chr1:46272488 [GRCh38]
Chr1:46738160 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1546G>A (p.Val516Ile) single nucleotide variant not specified [RCV004330331] Chr1:46273683 [GRCh38]
Chr1:46739355 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1493T>G (p.Met498Arg) single nucleotide variant not specified [RCV004330333] Chr1:46273630 [GRCh38]
Chr1:46739302 [GRCh37]
Chr1:1p34.1
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p34.1-33(chr1:46372688-47188150)x3 copy number gain not provided [RCV000736482] Chr1:46372688..47188150 [GRCh37]
Chr1:1p34.1-33
uncertain significance
NM_003579.4(RAD54L):c.1298del (p.Pro433fs) deletion Familial cancer of breast [RCV003448727] Chr1:46272724 [GRCh38]
Chr1:46738396 [GRCh37]
Chr1:1p34.1
likely pathogenic
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1
uncertain significance
GRCh37/hg19 1p34.1-33(chr1:46501759-46898503)x3 copy number gain not provided [RCV001005084] Chr1:46501759..46898503 [GRCh37]
Chr1:1p34.1-33
uncertain significance
NM_003579.4(RAD54L):c.1870-1G>A single nucleotide variant Non-Hodgkin lymphoma [RCV000986317] Chr1:46277816 [GRCh38]
Chr1:46743488 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.160C>G (p.Pro54Ala) single nucleotide variant Astrocytoma IDH-mutant [RCV003313905] Chr1:46250069 [GRCh38]
Chr1:46715741 [GRCh37]
Chr1:1p34.1
pathogenic|uncertain significance
NM_003579.4(RAD54L):c.796G>C (p.Val266Leu) single nucleotide variant Non-Hodgkin lymphoma [RCV000986315]|not specified [RCV004030110] Chr1:46261290 [GRCh38]
Chr1:46726962 [GRCh37]
Chr1:1p34.1
likely benign|uncertain significance
NM_003579.4(RAD54L):c.888C>T (p.Asp296=) single nucleotide variant Non-Hodgkin lymphoma [RCV000986316]|not provided [RCV004711495]|not specified [RCV004030111] Chr1:46261382 [GRCh38]
Chr1:46727054 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1900C>T (p.Arg634Cys) single nucleotide variant Premature ovarian failure [RCV001270184] Chr1:46277847 [GRCh38]
Chr1:46743519 [GRCh37]
Chr1:1p34.1
likely pathogenic
NM_003579.4(RAD54L):c.1138C>T (p.Arg380Trp) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002225807]|Premature ovarian failure [RCV001270182] Chr1:46270754 [GRCh38]
Chr1:46736426 [GRCh37]
Chr1:1p34.1
pathogenic|uncertain significance
NM_003579.4(RAD54L):c.1883A>C (p.Glu628Ala) single nucleotide variant Premature ovarian failure [RCV001270183] Chr1:46277830 [GRCh38]
Chr1:46743502 [GRCh37]
Chr1:1p34.1
likely pathogenic
NM_003579.4(RAD54L):c.604C>T (p.Arg202Cys) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV001374481]|RAD54L-related disorder [RCV003908480]|not provided [RCV004691400] Chr1:46260853 [GRCh38]
Chr1:46726525 [GRCh37]
Chr1:1p34.1
benign|uncertain significance
NM_003579.4(RAD54L):c.863del (p.Gly288fs) deletion Familial cancer of breast [RCV002244131] Chr1:46261356 [GRCh38]
Chr1:46727028 [GRCh37]
Chr1:1p34.1
uncertain significance
GRCh37/hg19 1p34.1-32.3(chr1:45303358-52157856) copy number loss not specified [RCV002053281] Chr1:45303358..52157856 [GRCh37]
Chr1:1p34.1-32.3
likely pathogenic
GRCh37/hg19 1p35.1-33(chr1:33285582-47891811) copy number gain not specified [RCV002052781] Chr1:33285582..47891811 [GRCh37]
Chr1:1p35.1-33
pathogenic
GRCh37/hg19 1p34.1(chr1:46083531-46738006) copy number gain not specified [RCV002053292] Chr1:46083531..46738006 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1611-51del deletion Hereditary breast ovarian cancer syndrome [RCV002226241] Chr1:46274080 [GRCh38]
Chr1:46739752 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2034-6C>T single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226251] Chr1:46278066 [GRCh38]
Chr1:46743738 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1042+78G>A single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226204]|not provided [RCV004711901] Chr1:46267687 [GRCh38]
Chr1:46733359 [GRCh37]
Chr1:1p34.1
benign|likely benign
NM_003579.4(RAD54L):c.1600C>T (p.Arg534Cys) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226235]|RAD54L-related disorder [RCV003896076]|not provided [RCV004715627]|not specified [RCV004047236] Chr1:46273737 [GRCh38]
Chr1:46739409 [GRCh37]
Chr1:1p34.1
benign|likely benign
NM_003579.4(RAD54L):c.1611-55T>A single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226244]|not provided [RCV004711903] Chr1:46274083 [GRCh38]
Chr1:46739755 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2063G>A (p.Arg688His) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226253]|not specified [RCV004047240] Chr1:46278101 [GRCh38]
Chr1:46743773 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1523C>T (p.Thr508Ile) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226234]|not specified [RCV004047235] Chr1:46273660 [GRCh38]
Chr1:46739332 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1611-71T>A single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226239] Chr1:46274067 [GRCh38]
Chr1:46739739 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2197T>G (p.Phe733Val) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226257]|not specified [RCV004047242] Chr1:46278235 [GRCh38]
Chr1:46743907 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.352T>C (p.Leu118=) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226312]|not specified [RCV004047243] Chr1:46260044 [GRCh38]
Chr1:46725716 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.366G>A (p.Glu122=) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226333]|not provided [RCV004711905]|not specified [RCV004047244] Chr1:46260058 [GRCh38]
Chr1:46725730 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1393_1395del (p.Asp465del) deletion Hereditary breast ovarian cancer syndrome [RCV002226225] Chr1:46273370..46273372 [GRCh38]
Chr1:46739042..46739044 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1487-75G>A single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226227] Chr1:46273549 [GRCh38]
Chr1:46739221 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.62A>G (p.Asp21Gly) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226188]|not provided [RCV004711899]|not specified [RCV004047230] Chr1:46248570 [GRCh38]
Chr1:46714242 [GRCh37]
Chr1:1p34.1
benign|likely benign
NM_003579.4(RAD54L):c.1042+55G>C single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226200]|not provided [RCV004714390] Chr1:46267664 [GRCh38]
Chr1:46733336 [GRCh37]
Chr1:1p34.1
benign
NM_003579.4(RAD54L):c.1375+32T>C single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226220] Chr1:46272834 [GRCh38]
Chr1:46738506 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1748T>C (p.Ile583Thr) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226247]|RAD54L-related disorder [RCV003971195]|not specified [RCV004047238] Chr1:46274596 [GRCh38]
Chr1:46740268 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2190C>T (p.Ala730=) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226256]|RAD54L-related disorder [RCV003971196]|not provided [RCV004714392]|not specified [RCV004047241] Chr1:46278228 [GRCh38]
Chr1:46743900 [GRCh37]
Chr1:1p34.1
benign
NM_003579.4(RAD54L):c.767-57G>T single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226403]|not provided [RCV004711909] Chr1:46261204 [GRCh38]
Chr1:46726876 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1299G>A (p.Pro433=) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226217]|RAD54L-related disorder [RCV003933698]|not provided [RCV004711902]|not specified [RCV004047233] Chr1:46272726 [GRCh38]
Chr1:46738398 [GRCh37]
Chr1:1p34.1
benign|likely benign
NM_003579.4(RAD54L):c.95C>G (p.Pro32Arg) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226224]|not specified [RCV004047234] Chr1:46250004 [GRCh38]
Chr1:46715676 [GRCh37]
Chr1:1p34.1
likely benign|uncertain significance
NM_003579.4(RAD54L):c.1487-11G>A single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226230] Chr1:46273613 [GRCh38]
Chr1:46739285 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2026C>T (p.His676Tyr) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226250]|not specified [RCV004047239] Chr1:46277973 [GRCh38]
Chr1:46743645 [GRCh37]
Chr1:1p34.1
likely benign|uncertain significance
NM_003579.4(RAD54L):c.460C>T (p.Arg154Trp) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226353] Chr1:46260594 [GRCh38]
Chr1:46726266 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.767A>T (p.Glu256Val) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226189]|not specified [RCV004047231] Chr1:46261261 [GRCh38]
Chr1:46726933 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.892-26C>T single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226194]|not provided [RCV004714389] Chr1:46267433 [GRCh38]
Chr1:46733105 [GRCh37]
Chr1:1p34.1
benign|likely benign
NM_003579.4(RAD54L):c.894A>G (p.Gly298=) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226196]|not provided [RCV004711900]|not specified [RCV004047232] Chr1:46267461 [GRCh38]
Chr1:46733133 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1245-61del deletion Hereditary breast ovarian cancer syndrome [RCV002226208] Chr1:46272610 [GRCh38]
Chr1:46738282 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1611-56T>A single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226243] Chr1:46274082 [GRCh38]
Chr1:46739754 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.272-21G>A single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226284]|not provided [RCV004711904] Chr1:46259943 [GRCh38]
Chr1:46725615 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.477+37G>T single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226397] Chr1:46260648 [GRCh38]
Chr1:46726320 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1245-38_1245-37delinsAT indel Hereditary breast ovarian cancer syndrome [RCV002226211] Chr1:46272634..46272635 [GRCh38]
Chr1:46738306..46738307 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1615T>C (p.Leu539=) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226245]|not provided [RCV004714391] Chr1:46274142 [GRCh38]
Chr1:46739814 [GRCh37]
Chr1:1p34.1
benign|likely benign
NM_003579.4(RAD54L):c.144G>C (p.Leu48=) single nucleotide variant Hereditary breast ovarian cancer syndrome [RCV002226246]|not specified [RCV004047237] Chr1:46250053 [GRCh38]
Chr1:46715725 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1099del (p.Ala367fs) deletion not specified [RCV002248149] Chr1:46270715 [GRCh38]
Chr1:46736387 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2164G>A (p.Ala722Thr) single nucleotide variant not specified [RCV004330309] Chr1:46278202 [GRCh38]
Chr1:46743874 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.622A>G (p.Lys208Glu) single nucleotide variant not specified [RCV004330310] Chr1:46260871 [GRCh38]
Chr1:46726543 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1508A>G (p.Tyr503Cys) single nucleotide variant not specified [RCV004330323] Chr1:46273645 [GRCh38]
Chr1:46739317 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1550T>C (p.Val517Ala) single nucleotide variant not specified [RCV004330324] Chr1:46273687 [GRCh38]
Chr1:46739359 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2229G>A (p.Gln743=) single nucleotide variant not specified [RCV004330335] Chr1:46278267 [GRCh38]
Chr1:46743939 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1184G>A (p.Arg395Lys) single nucleotide variant not specified [RCV004330336] Chr1:46272480 [GRCh38]
Chr1:46738152 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1073A>G (p.Glu358Gly) single nucleotide variant not specified [RCV004330339] Chr1:46270689 [GRCh38]
Chr1:46736361 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1138C>A (p.Arg380=) single nucleotide variant not specified [RCV004327925] Chr1:46270754 [GRCh38]
Chr1:46736426 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1926C>T (p.Ser642=) single nucleotide variant not specified [RCV004327931] Chr1:46277873 [GRCh38]
Chr1:46743545 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.909C>T (p.Asn303=) single nucleotide variant not specified [RCV004327932] Chr1:46267476 [GRCh38]
Chr1:46733148 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.880A>G (p.Ile294Val) single nucleotide variant not specified [RCV004327933] Chr1:46261374 [GRCh38]
Chr1:46727046 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.571C>A (p.Leu191Met) single nucleotide variant not specified [RCV004327941] Chr1:46260820 [GRCh38]
Chr1:46726492 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.38G>A (p.Arg13Lys) single nucleotide variant not specified [RCV004050362] Chr1:46248546 [GRCh38]
Chr1:46714218 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.375G>C (p.Pro125=) single nucleotide variant not specified [RCV004048029] Chr1:46260067 [GRCh38]
Chr1:46725739 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.621C>G (p.Cys207Trp) single nucleotide variant not specified [RCV004053406] Chr1:46260870 [GRCh38]
Chr1:46726542 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.362A>T (p.Tyr121Phe) single nucleotide variant not specified [RCV004049277] Chr1:46260054 [GRCh38]
Chr1:46725726 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.365A>C (p.Glu122Ala) single nucleotide variant not specified [RCV004049589] Chr1:46260057 [GRCh38]
Chr1:46725729 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.953G>C (p.Ser318Thr) single nucleotide variant not specified [RCV004056894] Chr1:46267520 [GRCh38]
Chr1:46733192 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1158C>T (p.Ser386=) single nucleotide variant not specified [RCV004048790] Chr1:46270774 [GRCh38]
Chr1:46736446 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.79C>A (p.Pro27Thr) single nucleotide variant not specified [RCV004055362] Chr1:46248587 [GRCh38]
Chr1:46714259 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.374C>G (p.Pro125Arg) single nucleotide variant not specified [RCV004048002] Chr1:46260066 [GRCh38]
Chr1:46725738 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.541A>G (p.Met181Val) single nucleotide variant not specified [RCV004053044] Chr1:46260790 [GRCh38]
Chr1:46726462 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.811C>A (p.Leu271Ile) single nucleotide variant not specified [RCV004055461] Chr1:46261305 [GRCh38]
Chr1:46726977 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1954G>A (p.Val652Ile) single nucleotide variant not specified [RCV004061504] Chr1:46277901 [GRCh38]
Chr1:46743573 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.977C>G (p.Thr326Ser) single nucleotide variant not specified [RCV004057596] Chr1:46267544 [GRCh38]
Chr1:46733216 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.510T>C (p.Ser170=) single nucleotide variant not specified [RCV004051031] Chr1:46260759 [GRCh38]
Chr1:46726431 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.282C>T (p.Gly94=) single nucleotide variant not specified [RCV004062359] Chr1:46259974 [GRCh38]
Chr1:46725646 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.369T>C (p.Pro123=) single nucleotide variant not specified [RCV004049697] Chr1:46260061 [GRCh38]
Chr1:46725733 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.810C>T (p.Ile270=) single nucleotide variant not specified [RCV004055456] Chr1:46261304 [GRCh38]
Chr1:46726976 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2046A>G (p.Arg682=) single nucleotide variant not specified [RCV004059621] Chr1:46278084 [GRCh38]
Chr1:46743756 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1140G>A (p.Arg380=) single nucleotide variant not specified [RCV004047957] Chr1:46270756 [GRCh38]
Chr1:46736428 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1326G>A (p.Met442Ile) single nucleotide variant not specified [RCV004058398] Chr1:46272753 [GRCh38]
Chr1:46738425 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.676T>G (p.Trp226Gly) single nucleotide variant not specified [RCV004052787] Chr1:46260925 [GRCh38]
Chr1:46726597 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.359T>C (p.Leu120Pro) single nucleotide variant not specified [RCV004049204] Chr1:46260051 [GRCh38]
Chr1:46725723 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.301A>C (p.Lys101Gln) single nucleotide variant not specified [RCV004065531] Chr1:46259993 [GRCh38]
Chr1:46725665 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.301A>G (p.Lys101Glu) single nucleotide variant not specified [RCV004065532] Chr1:46259993 [GRCh38]
Chr1:46725665 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1328G>C (p.Ser443Thr) single nucleotide variant Familial cancer of breast [RCV004785657]|not specified [RCV004058411] Chr1:46272755 [GRCh38]
Chr1:46738427 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1329T>C (p.Ser443=) single nucleotide variant not specified [RCV004058418] Chr1:46272756 [GRCh38]
Chr1:46738428 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2230C>T (p.Arg744Trp) single nucleotide variant not specified [RCV004061835] Chr1:46278268 [GRCh38]
Chr1:46743940 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2235C>A (p.Gly745=) single nucleotide variant not specified [RCV004061856] Chr1:46278273 [GRCh38]
Chr1:46743945 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2236C>G (p.Leu746Val) single nucleotide variant not specified [RCV004061862] Chr1:46278274 [GRCh38]
Chr1:46743946 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.511C>A (p.Arg171=) single nucleotide variant not specified [RCV004051042] Chr1:46260760 [GRCh38]
Chr1:46726432 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.223C>G (p.Arg75Gly) single nucleotide variant not specified [RCV004061875] Chr1:46258698 [GRCh38]
Chr1:46724370 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.224G>T (p.Arg75Leu) single nucleotide variant not specified [RCV004061908] Chr1:46258699 [GRCh38]
Chr1:46724371 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.543G>A (p.Met181Ile) single nucleotide variant not specified [RCV004053076] Chr1:46260792 [GRCh38]
Chr1:46726464 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.979C>T (p.Pro327Ser) single nucleotide variant not specified [RCV004057614] Chr1:46267546 [GRCh38]
Chr1:46733218 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1317G>A (p.Glu439=) single nucleotide variant not specified [RCV004058353] Chr1:46272744 [GRCh38]
Chr1:46738416 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2027A>G (p.His676Arg) single nucleotide variant not specified [RCV004059541] Chr1:46277974 [GRCh38]
Chr1:46743646 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2022C>T (p.Asp674=) single nucleotide variant not specified [RCV004059529] Chr1:46277969 [GRCh38]
Chr1:46743641 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1960C>T (p.Arg654Cys) single nucleotide variant not specified [RCV004061539] Chr1:46277907 [GRCh38]
Chr1:46743579 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1327A>T (p.Ser443Cys) single nucleotide variant not specified [RCV004058405] Chr1:46272754 [GRCh38]
Chr1:46738426 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2205C>T (p.Phe735=) single nucleotide variant not specified [RCV004061746] Chr1:46278243 [GRCh38]
Chr1:46743915 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.744G>A (p.Lys248=) single nucleotide variant not specified [RCV004056290] Chr1:46260993 [GRCh38]
Chr1:46726665 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1075T>C (p.Leu359=) single nucleotide variant not specified [RCV004059565] Chr1:46270691 [GRCh38]
Chr1:46736363 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.287G>A (p.Arg96Gln) single nucleotide variant not specified [RCV004063024] Chr1:46259979 [GRCh38]
Chr1:46725651 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.967A>G (p.Ile323Val) single nucleotide variant not specified [RCV004056999] Chr1:46267534 [GRCh38]
Chr1:46733206 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.958C>T (p.Arg320Trp) single nucleotide variant not specified [RCV004056934] Chr1:46267525 [GRCh38]
Chr1:46733197 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.257T>G (p.Ile86Ser) single nucleotide variant not specified [RCV004062805] Chr1:46258732 [GRCh38]
Chr1:46724404 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.267T>C (p.Tyr89=) single nucleotide variant not specified [RCV004063626] Chr1:46258742 [GRCh38]
Chr1:46724414 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1154C>T (p.Thr385Ile) single nucleotide variant not specified [RCV004048084] Chr1:46270770 [GRCh38]
Chr1:46736442 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.549T>C (p.Asp183=) single nucleotide variant not specified [RCV004053152] Chr1:46260798 [GRCh38]
Chr1:46726470 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1119C>A (p.Asp373Glu) single nucleotide variant not specified [RCV004062456] Chr1:46270735 [GRCh38]
Chr1:46736407 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.302A>G (p.Lys101Arg) single nucleotide variant not specified [RCV004065561] Chr1:46259994 [GRCh38]
Chr1:46725666 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2028T>C (p.His676=) single nucleotide variant not specified [RCV004059554] Chr1:46277975 [GRCh38]
Chr1:46743647 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.816C>A (p.Ile272=) single nucleotide variant not specified [RCV004055511] Chr1:46261310 [GRCh38]
Chr1:46726982 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.984C>T (p.Ile328=) single nucleotide variant not specified [RCV004057646] Chr1:46267551 [GRCh38]
Chr1:46733223 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.674A>G (p.Asn225Ser) single nucleotide variant not specified [RCV004052764] Chr1:46260923 [GRCh38]
Chr1:46726595 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1959G>A (p.Glu653=) single nucleotide variant not specified [RCV004061527] Chr1:46277906 [GRCh38]
Chr1:46743578 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1959G>C (p.Glu653Asp) single nucleotide variant not specified [RCV004061528] Chr1:46277906 [GRCh38]
Chr1:46743578 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1110T>A (p.Ser370Arg) single nucleotide variant not specified [RCV004063998] Chr1:46270726 [GRCh38]
Chr1:46736398 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.627A>G (p.Pro209=) single nucleotide variant not specified [RCV004053473] Chr1:46260876 [GRCh38]
Chr1:46726548 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1200T>C (p.Leu400=) single nucleotide variant not specified [RCV004053068] Chr1:46272496 [GRCh38]
Chr1:46738168 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.338T>A (p.Leu113Gln) single nucleotide variant not specified [RCV004047896] Chr1:46260030 [GRCh38]
Chr1:46725702 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1137G>T (p.Glu379Asp) single nucleotide variant not specified [RCV004049533] Chr1:46270753 [GRCh38]
Chr1:46736425 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.812T>C (p.Leu271Pro) single nucleotide variant not specified [RCV004055481] Chr1:46261306 [GRCh38]
Chr1:46726978 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1314T>G (p.Leu438=) single nucleotide variant not specified [RCV004058337] Chr1:46272741 [GRCh38]
Chr1:46738413 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.492G>A (p.Leu164=) single nucleotide variant not specified [RCV004050240] Chr1:46260741 [GRCh38]
Chr1:46726413 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.194T>C (p.Leu65Pro) single nucleotide variant not specified [RCV004061477] Chr1:46250103 [GRCh38]
Chr1:46715775 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.708G>A (p.Gly236=) single nucleotide variant not specified [RCV004055235] Chr1:46260957 [GRCh38]
Chr1:46726629 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1315G>A (p.Glu439Lys) single nucleotide variant not specified [RCV004058344] Chr1:46272742 [GRCh38]
Chr1:46738414 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.628G>C (p.Glu210Gln) single nucleotide variant not specified [RCV004053499] Chr1:46260877 [GRCh38]
Chr1:46726549 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.372C>T (p.Pro124=) single nucleotide variant not specified [RCV004049779] Chr1:46260064 [GRCh38]
Chr1:46725736 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.355G>A (p.Val119Ile) single nucleotide variant not specified [RCV004049123] Chr1:46260047 [GRCh38]
Chr1:46725719 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1950G>A (p.Gln650=) single nucleotide variant not specified [RCV004061486] Chr1:46277897 [GRCh38]
Chr1:46743569 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.805C>G (p.Pro269Ala) single nucleotide variant not specified [RCV004055410] Chr1:46261299 [GRCh38]
Chr1:46726971 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.70G>T (p.Asp24Tyr) single nucleotide variant not specified [RCV004055259] Chr1:46248578 [GRCh38]
Chr1:46714250 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.972C>T (p.Ser324=) single nucleotide variant not specified [RCV004057555] Chr1:46267539 [GRCh38]
Chr1:46733211 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1054G>A (p.Glu352Lys) single nucleotide variant not specified [RCV004059937] Chr1:46270670 [GRCh38]
Chr1:46736342 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1704C>T (p.Val568=) single nucleotide variant not specified [RCV004060531] Chr1:46274552 [GRCh38]
Chr1:46740224 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.186A>G (p.Pro62=) single nucleotide variant not specified [RCV004060097] Chr1:46250095 [GRCh38]
Chr1:46715767 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1871C>T (p.Ala624Val) single nucleotide variant not specified [RCV004060109] Chr1:46277818 [GRCh38]
Chr1:46743490 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.569C>T (p.Thr190Met) single nucleotide variant not specified [RCV004053717] Chr1:46260818 [GRCh38]
Chr1:46726490 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.56C>G (p.Ser19Cys) single nucleotide variant not specified [RCV004053724] Chr1:46248564 [GRCh38]
Chr1:46714236 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.570G>T (p.Thr190=) single nucleotide variant not specified [RCV004053738] Chr1:46260819 [GRCh38]
Chr1:46726491 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.499T>C (p.Cys167Arg) single nucleotide variant not specified [RCV004050864] Chr1:46260748 [GRCh38]
Chr1:46726420 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.49G>A (p.Gly17Ser) single nucleotide variant not specified [RCV004050868] Chr1:46248557 [GRCh38]
Chr1:46714229 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.415C>T (p.Leu139Phe) single nucleotide variant not specified [RCV004051804] Chr1:46260549 [GRCh38]
Chr1:46726221 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.417C>T (p.Leu139=) single nucleotide variant not specified [RCV004051844] Chr1:46260551 [GRCh38]
Chr1:46726223 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2019T>A (p.Ser673Arg) single nucleotide variant not specified [RCV004059511] Chr1:46277966 [GRCh38]
Chr1:46743638 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2111C>G (p.Ala704Gly) single nucleotide variant not specified [RCV004060368] Chr1:46278149 [GRCh38]
Chr1:46743821 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2113G>A (p.Gly705Arg) single nucleotide variant not specified [RCV004060375] Chr1:46278151 [GRCh38]
Chr1:46743823 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2156T>C (p.Val719Ala) single nucleotide variant not specified [RCV004061054] Chr1:46278194 [GRCh38]
Chr1:46743866 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.528C>T (p.Ser176=) single nucleotide variant not specified [RCV004052338] Chr1:46260777 [GRCh38]
Chr1:46726449 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1830T>C (p.Asp610=) single nucleotide variant not specified [RCV004059421] Chr1:46274678 [GRCh38]
Chr1:46740350 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2167G>A (p.Ala723Thr) single nucleotide variant not specified [RCV004061089] Chr1:46278205 [GRCh38]
Chr1:46743877 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1844C>T (p.Thr615Ile) single nucleotide variant not specified [RCV004059993] Chr1:46274692 [GRCh38]
Chr1:46740364 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1858C>G (p.Arg620Gly) single nucleotide variant not specified [RCV004060050] Chr1:46274706 [GRCh38]
Chr1:46740378 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1681A>C (p.Ser561Arg) single nucleotide variant not specified [RCV004059875] Chr1:46274208 [GRCh38]
Chr1:46739880 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.351C>T (p.Ala117=) single nucleotide variant not specified [RCV004048723] Chr1:46260043 [GRCh38]
Chr1:46725715 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1574C>T (p.Thr525Ile) single nucleotide variant not specified [RCV004057283] Chr1:46273711 [GRCh38]
Chr1:46739383 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.216A>G (p.Ala72=) single nucleotide variant not specified [RCV004061100] Chr1:46258691 [GRCh38]
Chr1:46724363 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.211G>A (p.Glu71Lys) single nucleotide variant not specified [RCV004060396] Chr1:46258686 [GRCh38]
Chr1:46724358 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2121C>T (p.Asn707=) single nucleotide variant not specified [RCV004060403] Chr1:46278159 [GRCh38]
Chr1:46743831 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2124C>G (p.His708Gln) single nucleotide variant not specified [RCV004060413] Chr1:46278162 [GRCh38]
Chr1:46743834 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2124C>T (p.His708=) single nucleotide variant not specified [RCV004060414] Chr1:46278162 [GRCh38]
Chr1:46743834 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2125T>C (p.Cys709Arg) single nucleotide variant not specified [RCV004060423] Chr1:46278163 [GRCh38]
Chr1:46743835 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2128A>G (p.Thr710Ala) single nucleotide variant not specified [RCV004060429] Chr1:46278166 [GRCh38]
Chr1:46743838 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2129C>T (p.Thr710Ile) single nucleotide variant not specified [RCV004060436] Chr1:46278167 [GRCh38]
Chr1:46743839 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1343C>G (p.Ser448Cys) single nucleotide variant not specified [RCV004058743] Chr1:46272770 [GRCh38]
Chr1:46738442 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.512G>A (p.Arg171Gln) single nucleotide variant not specified [RCV004051058] Chr1:46260761 [GRCh38]
Chr1:46726433 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.512G>T (p.Arg171Leu) single nucleotide variant not specified [RCV004051059] Chr1:46260761 [GRCh38]
Chr1:46726433 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2132A>G (p.Asp711Gly) single nucleotide variant not specified [RCV004060449] Chr1:46278170 [GRCh38]
Chr1:46743842 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2136G>A (p.Lys712=) single nucleotide variant not specified [RCV004060465] Chr1:46278174 [GRCh38]
Chr1:46743846 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1347C>T (p.Ser449=) single nucleotide variant not specified [RCV004058761] Chr1:46272774 [GRCh38]
Chr1:46738446 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2078C>T (p.Pro693Leu) single nucleotide variant not specified [RCV004060246] Chr1:46278116 [GRCh38]
Chr1:46743788 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.953G>A (p.Ser318Asn) single nucleotide variant not specified [RCV004056893] Chr1:46267520 [GRCh38]
Chr1:46733192 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.69A>G (p.Glu23=) single nucleotide variant not specified [RCV004055101] Chr1:46248577 [GRCh38]
Chr1:46714249 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.514C>T (p.Arg172Cys) single nucleotide variant not specified [RCV004051091] Chr1:46260763 [GRCh38]
Chr1:46726435 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1224T>G (p.Ile408Met) single nucleotide variant not specified [RCV004054350] Chr1:46272520 [GRCh38]
Chr1:46738192 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.251T>C (p.Val84Ala) single nucleotide variant not specified [RCV004062082] Chr1:46258726 [GRCh38]
Chr1:46724398 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.315C>G (p.Val105=) single nucleotide variant not specified [RCV004048498] Chr1:46260007 [GRCh38]
Chr1:46725679 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.394C>T (p.Leu132=) single nucleotide variant not specified [RCV004050456] Chr1:46260086 [GRCh38]
Chr1:46725758 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1391A>G (p.Tyr464Cys) single nucleotide variant not specified [RCV004057092] Chr1:46273370 [GRCh38]
Chr1:46739042 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1400G>A (p.Cys467Tyr) single nucleotide variant not specified [RCV004057138] Chr1:46273379 [GRCh38]
Chr1:46739051 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.615A>G (p.Pro205=) single nucleotide variant not specified [RCV004053334] Chr1:46260864 [GRCh38]
Chr1:46726536 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.598C>T (p.Leu200Phe) single nucleotide variant not specified [RCV004052528] Chr1:46260847 [GRCh38]
Chr1:46726519 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1644C>T (p.Ser548=) single nucleotide variant not specified [RCV004058154] Chr1:46274171 [GRCh38]
Chr1:46739843 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.325C>T (p.Leu109Phe) single nucleotide variant not specified [RCV004049380] Chr1:46260017 [GRCh38]
Chr1:46725689 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.864A>C (p.Gly288=) single nucleotide variant not specified [RCV004056583] Chr1:46261358 [GRCh38]
Chr1:46727030 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.921G>C (p.Gln307His) single nucleotide variant not specified [RCV004055607] Chr1:46267488 [GRCh38]
Chr1:46733160 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1973T>C (p.Leu658Pro) single nucleotide variant not specified [RCV004061603] Chr1:46277920 [GRCh38]
Chr1:46743592 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.422T>A (p.Val141Asp) single nucleotide variant not specified [RCV004051936] Chr1:46260556 [GRCh38]
Chr1:46726228 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.84C>A (p.Gly28=) single nucleotide variant not specified [RCV004056192] Chr1:46248592 [GRCh38]
Chr1:46714264 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.198C>T (p.Asp66=) single nucleotide variant not specified [RCV004061672] Chr1:46250107 [GRCh38]
Chr1:46715779 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1494G>A (p.Met498Ile) single nucleotide variant not specified [RCV004058511] Chr1:46273631 [GRCh38]
Chr1:46739303 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.889G>A (p.Glu297Lys) single nucleotide variant not specified [RCV004054843] Chr1:46261383 [GRCh38]
Chr1:46727055 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1263T>C (p.Thr421=) single nucleotide variant not specified [RCV004056208] Chr1:46272690 [GRCh38]
Chr1:46738362 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.647T>C (p.Val216Ala) single nucleotide variant not specified [RCV004054047] Chr1:46260896 [GRCh38]
Chr1:46726568 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.936G>A (p.Leu312=) single nucleotide variant not specified [RCV004055714] Chr1:46267503 [GRCh38]
Chr1:46733175 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.88G>A (p.Val30Met) single nucleotide variant not specified [RCV004054849] Chr1:46248596 [GRCh38]
Chr1:46714268 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.308C>G (p.Ala103Gly) single nucleotide variant not specified [RCV004048288] Chr1:46260000 [GRCh38]
Chr1:46725672 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1735G>C (p.Gly579Arg) single nucleotide variant not specified [RCV004060701] Chr1:46274583 [GRCh38]
Chr1:46740255 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.834C>T (p.Phe278=) single nucleotide variant not specified [RCV004056063] Chr1:46261328 [GRCh38]
Chr1:46727000 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.381C>T (p.Ser127=) single nucleotide variant not specified [RCV004048148] Chr1:46260073 [GRCh38]
Chr1:46725745 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1448C>G (p.Pro483Arg) single nucleotide variant not specified [RCV004057889] Chr1:46273427 [GRCh38]
Chr1:46739099 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.317G>C (p.Arg106Pro) single nucleotide variant not specified [RCV004048847] Chr1:46260009 [GRCh38]
Chr1:46725681 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1607G>A (p.Arg536Gln) single nucleotide variant not specified [RCV004057451] Chr1:46273744 [GRCh38]
Chr1:46739416 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.573G>A (p.Leu191=) single nucleotide variant not specified [RCV004053771] Chr1:46260822 [GRCh38]
Chr1:46726494 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.385C>T (p.His129Tyr) single nucleotide variant not specified [RCV004599290] Chr1:46260077 [GRCh38]
Chr1:46725749 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1116A>C (p.Ala372=) single nucleotide variant not specified [RCV004062273] Chr1:46270732 [GRCh38]
Chr1:46736404 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1455C>T (p.Tyr485=) single nucleotide variant not specified [RCV004057929] Chr1:46273434 [GRCh38]
Chr1:46739106 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.730G>T (p.Asp244Tyr) single nucleotide variant not specified [RCV004055881] Chr1:46260979 [GRCh38]
Chr1:46726651 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1137G>A (p.Glu379=) single nucleotide variant not specified [RCV004049521] Chr1:46270753 [GRCh38]
Chr1:46736425 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.980C>T (p.Pro327Leu) single nucleotide variant not specified [RCV004057623] Chr1:46267547 [GRCh38]
Chr1:46733219 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1593G>A (p.Lys531=) single nucleotide variant not specified [RCV004057376] Chr1:46273730 [GRCh38]
Chr1:46739402 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.333C>A (p.Asp111Glu) single nucleotide variant not specified [RCV004599282] Chr1:46260025 [GRCh38]
Chr1:46725697 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1995T>C (p.Phe665=) single nucleotide variant not specified [RCV004061694] Chr1:46277942 [GRCh38]
Chr1:46743614 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1996A>G (p.Ile666Val) single nucleotide variant not specified [RCV004061698] Chr1:46277943 [GRCh38]
Chr1:46743615 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1998C>G (p.Ile666Met) single nucleotide variant not specified [RCV004061705] Chr1:46277945 [GRCh38]
Chr1:46743617 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.199A>G (p.Ser67Gly) single nucleotide variant not specified [RCV004061715] Chr1:46250108 [GRCh38]
Chr1:46715780 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2199C>T (p.Phe733=) single nucleotide variant not specified [RCV004061198] Chr1:46278237 [GRCh38]
Chr1:46743909 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.580A>C (p.Ile194Leu) single nucleotide variant not specified [RCV004054128] Chr1:46260829 [GRCh38]
Chr1:46726501 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1566C>T (p.Tyr522=) single nucleotide variant not specified [RCV004059161] Chr1:46273703 [GRCh38]
Chr1:46739375 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2004T>A (p.Asp668Glu) single nucleotide variant not specified [RCV004059478] Chr1:46277951 [GRCh38]
Chr1:46743623 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1414G>A (p.Asp472Asn) single nucleotide variant not specified [RCV004057199] Chr1:46273393 [GRCh38]
Chr1:46739065 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.108A>G (p.Lys36=) single nucleotide variant not specified [RCV004061969] Chr1:46250017 [GRCh38]
Chr1:46715689 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1645A>G (p.Ile549Val) single nucleotide variant not specified [RCV004058157] Chr1:46274172 [GRCh38]
Chr1:46739844 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1273A>G (p.Lys425Glu) single nucleotide variant not specified [RCV004055028] Chr1:46272700 [GRCh38]
Chr1:46738372 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.845T>C (p.Val282Ala) single nucleotide variant not specified [RCV004056161] Chr1:46261339 [GRCh38]
Chr1:46727011 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.429G>A (p.Val143=) single nucleotide variant not specified [RCV004049945] Chr1:46260563 [GRCh38]
Chr1:46726235 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1974G>A (p.Leu658=) single nucleotide variant not specified [RCV004061606] Chr1:46277921 [GRCh38]
Chr1:46743593 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2212C>T (p.Arg738Cys) single nucleotide variant not specified [RCV004061766] Chr1:46278250 [GRCh38]
Chr1:46743922 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2213G>C (p.Arg738Pro) single nucleotide variant not specified [RCV004061773] Chr1:46278251 [GRCh38]
Chr1:46743923 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2213G>T (p.Arg738Leu) single nucleotide variant not specified [RCV004061774] Chr1:46278251 [GRCh38]
Chr1:46743923 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.853C>T (p.Leu285Phe) single nucleotide variant not specified [RCV004056232] Chr1:46261347 [GRCh38]
Chr1:46727019 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.296G>C (p.Gly99Ala) single nucleotide variant not specified [RCV004065396] Chr1:46259988 [GRCh38]
Chr1:46725660 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.5G>C (p.Arg2Thr) single nucleotide variant not specified [RCV004052558] Chr1:46248513 [GRCh38]
Chr1:46714185 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1569C>A (p.Thr523=) single nucleotide variant not specified [RCV004059177] Chr1:46273706 [GRCh38]
Chr1:46739378 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.940A>G (p.Ser314Gly) single nucleotide variant not specified [RCV004056780] Chr1:46267507 [GRCh38]
Chr1:46733179 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.177C>T (p.Thr59=) single nucleotide variant not specified [RCV004061435] Chr1:46250086 [GRCh38]
Chr1:46715758 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.857A>T (p.Gln286Leu) single nucleotide variant not specified [RCV004056523] Chr1:46261351 [GRCh38]
Chr1:46727023 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.867T>C (p.Ser289=) single nucleotide variant not specified [RCV004056625] Chr1:46261361 [GRCh38]
Chr1:46727033 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.467A>C (p.His156Pro) single nucleotide variant not specified [RCV004051621] Chr1:46260601 [GRCh38]
Chr1:46726273 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.723G>A (p.Leu241=) single nucleotide variant not specified [RCV004055798] Chr1:46260972 [GRCh38]
Chr1:46726644 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.597A>C (p.Thr199=) single nucleotide variant not specified [RCV004052510] Chr1:46260846 [GRCh38]
Chr1:46726518 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1601G>A (p.Arg534His) single nucleotide variant RAD54L-related disorder [RCV003926389]|not specified [RCV004057423] Chr1:46273738 [GRCh38]
Chr1:46739410 [GRCh37]
Chr1:1p34.1
benign|likely benign
NM_003579.4(RAD54L):c.311G>A (p.Gly104Glu) single nucleotide variant not specified [RCV004048388] Chr1:46260003 [GRCh38]
Chr1:46725675 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.894A>T (p.Gly298=) single nucleotide variant not specified [RCV004054885] Chr1:46267461 [GRCh38]
Chr1:46733133 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.687G>A (p.Glu229=) single nucleotide variant not specified [RCV004052906] Chr1:46260936 [GRCh38]
Chr1:46726608 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.760A>G (p.Lys254Glu) single nucleotide variant not specified [RCV004056448] Chr1:46261009 [GRCh38]
Chr1:46726681 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1673G>A (p.Arg558His) single nucleotide variant not specified [RCV004059843] Chr1:46274200 [GRCh38]
Chr1:46739872 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2181C>T (p.Ala727=) single nucleotide variant not specified [RCV004061148] Chr1:46278219 [GRCh38]
Chr1:46743891 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1965C>T (p.His655=) single nucleotide variant not specified [RCV004061560] Chr1:46277912 [GRCh38]
Chr1:46743584 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.341A>G (p.Glu114Gly) single nucleotide variant not specified [RCV004047973] Chr1:46260033 [GRCh38]
Chr1:46725705 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.753A>G (p.Ile251Met) single nucleotide variant not specified [RCV004056377] Chr1:46261002 [GRCh38]
Chr1:46726674 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1707C>T (p.Phe569=) single nucleotide variant not specified [RCV004060551] Chr1:46274555 [GRCh38]
Chr1:46740227 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.707G>A (p.Gly236Glu) single nucleotide variant not specified [RCV004055222] Chr1:46260956 [GRCh38]
Chr1:46726628 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2051G>A (p.Cys684Tyr) single nucleotide variant not specified [RCV004059649] Chr1:46278089 [GRCh38]
Chr1:46743761 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.94C>T (p.Pro32Ser) single nucleotide variant not specified [RCV004056863] Chr1:46250003 [GRCh38]
Chr1:46715675 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.950C>T (p.Thr317Ile) single nucleotide variant not specified [RCV004056870] Chr1:46267517 [GRCh38]
Chr1:46733189 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.469C>A (p.Gln157Lys) single nucleotide variant not specified [RCV004051997] Chr1:46260603 [GRCh38]
Chr1:46726275 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1793C>T (p.Ala598Val) single nucleotide variant not specified [RCV004059235] Chr1:46274641 [GRCh38]
Chr1:46740313 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1061A>G (p.Lys354Arg) single nucleotide variant not specified [RCV004059254] Chr1:46270677 [GRCh38]
Chr1:46736349 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1224T>C (p.Ile408=) single nucleotide variant not specified [RCV004054341] Chr1:46272520 [GRCh38]
Chr1:46738192 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.618G>A (p.Glu206=) single nucleotide variant not specified [RCV004053382] Chr1:46260867 [GRCh38]
Chr1:46726539 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.605G>A (p.Arg202His) single nucleotide variant not specified [RCV004052644] Chr1:46260854 [GRCh38]
Chr1:46726526 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1165A>G (p.Asn389Asp) single nucleotide variant not specified [RCV004051713] Chr1:46270781 [GRCh38]
Chr1:46736453 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.227G>C (p.Ser76Thr) single nucleotide variant not specified [RCV004599387] Chr1:46258702 [GRCh38]
Chr1:46724374 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1669G>C (p.Glu557Gln) single nucleotide variant not specified [RCV004059817] Chr1:46274196 [GRCh38]
Chr1:46739868 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1578G>A (p.Leu526=) single nucleotide variant not specified [RCV004057295] Chr1:46273715 [GRCh38]
Chr1:46739387 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1500C>A (p.Val500=) single nucleotide variant not specified [RCV004058543] Chr1:46273637 [GRCh38]
Chr1:46739309 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.952A>T (p.Ser318Cys) single nucleotide variant not specified [RCV004056887] Chr1:46267519 [GRCh38]
Chr1:46733191 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.923C>T (p.Thr308Ile) single nucleotide variant not specified [RCV004055623] Chr1:46267490 [GRCh38]
Chr1:46733162 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1429G>T (p.Ala477Ser) single nucleotide variant not specified [RCV004599345] Chr1:46273408 [GRCh38]
Chr1:46739080 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.937G>C (p.Asp313His) single nucleotide variant not specified [RCV004055720] Chr1:46267504 [GRCh38]
Chr1:46733176 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.758A>G (p.Gln253Arg) single nucleotide variant not specified [RCV004056425] Chr1:46261007 [GRCh38]
Chr1:46726679 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.613C>G (p.Pro205Ala) single nucleotide variant not specified [RCV004053302] Chr1:46260862 [GRCh38]
Chr1:46726534 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1482G>A (p.Leu494=) single nucleotide variant not specified [RCV004058456] Chr1:46273461 [GRCh38]
Chr1:46739133 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1482G>T (p.Leu494=) single nucleotide variant not specified [RCV004058458] Chr1:46273461 [GRCh38]
Chr1:46739133 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.24C>G (p.Ser8Arg) single nucleotide variant not specified [RCV004062012] Chr1:46248532 [GRCh38]
Chr1:46714204 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2176G>A (p.Ala726Thr) single nucleotide variant not specified [RCV004061129] Chr1:46278214 [GRCh38]
Chr1:46743886 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.865A>G (p.Ser289Gly) single nucleotide variant not specified [RCV004056602] Chr1:46261359 [GRCh38]
Chr1:46727031 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2074C>T (p.Pro692Ser) single nucleotide variant not specified [RCV004060233] Chr1:46278112 [GRCh38]
Chr1:46743784 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1095A>G (p.Arg365=) single nucleotide variant not specified [RCV004063320] Chr1:46270711 [GRCh38]
Chr1:46736383 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.956G>A (p.Arg319Gln) single nucleotide variant not specified [RCV004056922] Chr1:46267523 [GRCh38]
Chr1:46733195 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.103C>T (p.Arg35Trp) single nucleotide variant not specified [RCV004058476] Chr1:46250012 [GRCh38]
Chr1:46715684 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1432T>C (p.Leu478=) single nucleotide variant not specified [RCV004057812] Chr1:46273411 [GRCh38]
Chr1:46739083 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2221G>A (p.Glu741Lys) single nucleotide variant not specified [RCV004061807] Chr1:46278259 [GRCh38]
Chr1:46743931 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1531C>T (p.Arg511Cys) single nucleotide variant not specified [RCV004058962] Chr1:46273668 [GRCh38]
Chr1:46739340 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1533T>C (p.Arg511=) single nucleotide variant not specified [RCV004058974] Chr1:46273670 [GRCh38]
Chr1:46739342 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1671A>C (p.Glu557Asp) single nucleotide variant not specified [RCV004059829] Chr1:46274198 [GRCh38]
Chr1:46739870 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2177C>T (p.Ala726Val) single nucleotide variant not specified [RCV004061132] Chr1:46278215 [GRCh38]
Chr1:46743887 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1672C>T (p.Arg558Cys) single nucleotide variant not specified [RCV004059838] Chr1:46274199 [GRCh38]
Chr1:46739871 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.993T>G (p.Asp331Glu) single nucleotide variant not specified [RCV004057714] Chr1:46267560 [GRCh38]
Chr1:46733232 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.100A>C (p.Lys34Gln) single nucleotide variant not specified [RCV004064142] Chr1:46250009 [GRCh38]
Chr1:46715681 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.586T>C (p.Leu196=) single nucleotide variant not specified [RCV004054210] Chr1:46260835 [GRCh38]
Chr1:46726507 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.966C>T (p.Leu322=) single nucleotide variant not specified [RCV004056993] Chr1:46267533 [GRCh38]
Chr1:46733205 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1385T>C (p.Leu462Pro) single nucleotide variant not specified [RCV004057047] Chr1:46273364 [GRCh38]
Chr1:46739036 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1250C>G (p.Thr417Arg) single nucleotide variant not specified [RCV004599327] Chr1:46272677 [GRCh38]
Chr1:46738349 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.780C>T (p.Asn260=) single nucleotide variant not specified [RCV004054699] Chr1:46261274 [GRCh38]
Chr1:46726946 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1981T>G (p.Leu661Val) single nucleotide variant not specified [RCV004061644] Chr1:46277928 [GRCh38]
Chr1:46743600 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1036A>G (p.Ile346Val) single nucleotide variant not specified [RCV004057838] Chr1:46267603 [GRCh38]
Chr1:46733275 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.861A>G (p.Lys287=) single nucleotide variant not specified [RCV004056555] Chr1:46261355 [GRCh38]
Chr1:46727027 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.996G>C (p.Leu332=) single nucleotide variant not specified [RCV004057728] Chr1:46267563 [GRCh38]
Chr1:46733235 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.835C>G (p.Arg279Gly) single nucleotide variant not specified [RCV004056074] Chr1:46261329 [GRCh38]
Chr1:46727001 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.382G>A (p.Ala128Thr) single nucleotide variant not specified [RCV004048171] Chr1:46260074 [GRCh38]
Chr1:46725746 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.27G>C (p.Gln9His) single nucleotide variant not specified [RCV004062259] Chr1:46248535 [GRCh38]
Chr1:46714207 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1388T>A (p.Ile463Asn) single nucleotide variant not specified [RCV004057067] Chr1:46273367 [GRCh38]
Chr1:46739039 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.903C>G (p.Leu301=) single nucleotide variant not specified [RCV004054943] Chr1:46267470 [GRCh38]
Chr1:46733142 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1389C>G (p.Ile463Met) single nucleotide variant not specified [RCV004057069] Chr1:46273368 [GRCh38]
Chr1:46739040 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.731A>G (p.Asp244Gly) single nucleotide variant not specified [RCV004055893] Chr1:46260980 [GRCh38]
Chr1:46726652 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.732T>C (p.Asp244=) single nucleotide variant not specified [RCV004055911] Chr1:46260981 [GRCh38]
Chr1:46726653 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.235T>G (p.Ser79Ala) single nucleotide variant not specified [RCV004063293] Chr1:46258710 [GRCh38]
Chr1:46724382 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1694C>T (p.Pro565Leu) single nucleotide variant not specified [RCV004059957] Chr1:46274542 [GRCh38]
Chr1:46740214 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1626C>A (p.Arg542=) single nucleotide variant not specified [RCV004058050] Chr1:46274153 [GRCh38]
Chr1:46739825 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.776T>G (p.Met259Arg) single nucleotide variant not specified [RCV004054666] Chr1:46261270 [GRCh38]
Chr1:46726942 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.777G>T (p.Met259Ile) single nucleotide variant not specified [RCV004054674] Chr1:46261271 [GRCh38]
Chr1:46726943 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1758C>A (p.Asn586Lys) single nucleotide variant not specified [RCV004061322] Chr1:46274606 [GRCh38]
Chr1:46740278 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.837C>G (p.Arg279=) single nucleotide variant not specified [RCV004056090] Chr1:46261331 [GRCh38]
Chr1:46727003 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.196G>A (p.Asp66Asn) single nucleotide variant not specified [RCV004061583] Chr1:46250105 [GRCh38]
Chr1:46715777 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1408G>A (p.Glu470Lys) single nucleotide variant not specified [RCV004057167] Chr1:46273387 [GRCh38]
Chr1:46739059 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1032C>T (p.Ser344=) single nucleotide variant not specified [RCV004057083] Chr1:46267599 [GRCh38]
Chr1:46733271 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1641G>A (p.Met547Ile) single nucleotide variant not specified [RCV004058140] Chr1:46274168 [GRCh38]
Chr1:46739840 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1460C>T (p.Ser487Phe) single nucleotide variant not specified [RCV004057961] Chr1:46273439 [GRCh38]
Chr1:46739111 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1584C>T (p.Leu528=) single nucleotide variant not specified [RCV004057322] Chr1:46273721 [GRCh38]
Chr1:46739393 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1891A>G (p.Ile631Val) single nucleotide variant not specified [RCV004060204] Chr1:46277838 [GRCh38]
Chr1:46743510 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1343C>A (p.Ser448Tyr) single nucleotide variant not specified [RCV004058742] Chr1:46272770 [GRCh38]
Chr1:46738442 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1992G>A (p.Leu664=) single nucleotide variant not specified [RCV004061684] Chr1:46277939 [GRCh38]
Chr1:46743611 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1495C>A (p.Leu499Met) single nucleotide variant not specified [RCV004058515] Chr1:46273632 [GRCh38]
Chr1:46739304 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.933C>T (p.Ala311=) single nucleotide variant not specified [RCV004055696] Chr1:46267500 [GRCh38]
Chr1:46733172 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1517C>T (p.Ala506Val) single nucleotide variant not specified [RCV004058635] Chr1:46273654 [GRCh38]
Chr1:46739326 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1518G>C (p.Ala506=) single nucleotide variant not specified [RCV004058640] Chr1:46273655 [GRCh38]
Chr1:46739327 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1740C>T (p.Leu580=) single nucleotide variant not specified [RCV004061224] Chr1:46274588 [GRCh38]
Chr1:46740260 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1742A>G (p.Asn581Ser) single nucleotide variant not specified [RCV004061237] Chr1:46274590 [GRCh38]
Chr1:46740262 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.317G>A (p.Arg106His) single nucleotide variant not specified [RCV004048845] Chr1:46260009 [GRCh38]
Chr1:46725681 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1194T>A (p.Asp398Glu) single nucleotide variant not specified [RCV004051100] Chr1:46272490 [GRCh38]
Chr1:46738162 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1381G>A (p.Ala461Thr) single nucleotide variant not specified [RCV004057024] Chr1:46273360 [GRCh38]
Chr1:46739032 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.105G>T (p.Arg35=) single nucleotide variant not specified [RCV004061443] Chr1:46250014 [GRCh38]
Chr1:46715686 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1767C>T (p.Val589=) single nucleotide variant not specified [RCV004061368] Chr1:46274615 [GRCh38]
Chr1:46740287 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2146C>T (p.Arg716Trp) single nucleotide variant not specified [RCV004061010] Chr1:46278184 [GRCh38]
Chr1:46743856 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.324C>A (p.Ala108=) single nucleotide variant not specified [RCV004049346] Chr1:46260016 [GRCh38]
Chr1:46725688 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.736G>A (p.Gly246Arg) single nucleotide variant not specified [RCV004055950] Chr1:46260985 [GRCh38]
Chr1:46726657 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1556T>C (p.Val519Ala) single nucleotide variant not specified [RCV004059097] Chr1:46273693 [GRCh38]
Chr1:46739365 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.657T>C (p.Pro219=) single nucleotide variant not specified [RCV004054430] Chr1:46260906 [GRCh38]
Chr1:46726578 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1894T>C (p.Phe632Leu) single nucleotide variant not specified [RCV004060219] Chr1:46277841 [GRCh38]
Chr1:46743513 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1099G>A (p.Ala367Thr) single nucleotide variant not specified [RCV004063885] Chr1:46270715 [GRCh38]
Chr1:46736387 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1079C>G (p.Pro360Arg) single nucleotide variant not specified [RCV004060292] Chr1:46270695 [GRCh38]
Chr1:46736367 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.313G>A (p.Val105Ile) single nucleotide variant not specified [RCV004048448] Chr1:46260005 [GRCh38]
Chr1:46725677 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1521G>T (p.Val507=) single nucleotide variant not specified [RCV004058656] Chr1:46273658 [GRCh38]
Chr1:46739330 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.703G>A (p.Gly235Arg) single nucleotide variant not specified [RCV004055178] Chr1:46260952 [GRCh38]
Chr1:46726624 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1734T>C (p.Cys578=) single nucleotide variant not specified [RCV004060697] Chr1:46274582 [GRCh38]
Chr1:46740254 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1195A>G (p.Ile399Val) single nucleotide variant not specified [RCV004051632] Chr1:46272491 [GRCh38]
Chr1:46738163 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.452A>T (p.Lys151Met) single nucleotide variant not specified [RCV004051377] Chr1:46260586 [GRCh38]
Chr1:46726258 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1286G>T (p.Arg429Ile) single nucleotide variant not specified [RCV004057774] Chr1:46272713 [GRCh38]
Chr1:46738385 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1794C>T (p.Ala598=) single nucleotide variant not specified [RCV004059241] Chr1:46274642 [GRCh38]
Chr1:46740314 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.929A>G (p.Gln310Arg) single nucleotide variant not specified [RCV004055659] Chr1:46267496 [GRCh38]
Chr1:46733168 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.641C>A (p.Ala214Glu) single nucleotide variant not specified [RCV004053964] Chr1:46260890 [GRCh38]
Chr1:46726562 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1592A>C (p.Lys531Thr) single nucleotide variant not specified [RCV004057367] Chr1:46273729 [GRCh38]
Chr1:46739401 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1011C>T (p.Ser337=) single nucleotide variant not specified [RCV004047747] Chr1:46267578 [GRCh38]
Chr1:46733250 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1704C>A (p.Val568=) single nucleotide variant not specified [RCV004060530] Chr1:46274552 [GRCh38]
Chr1:46740224 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.660C>T (p.Ser220=) single nucleotide variant not specified [RCV004054455] Chr1:46260909 [GRCh38]
Chr1:46726581 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1509T>C (p.Tyr503=) single nucleotide variant not specified [RCV004058578] Chr1:46273646 [GRCh38]
Chr1:46739318 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.318C>T (p.Arg106=) single nucleotide variant not specified [RCV004048879] Chr1:46260010 [GRCh38]
Chr1:46725682 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1555G>C (p.Val519Leu) single nucleotide variant not specified [RCV004059090] Chr1:46273692 [GRCh38]
Chr1:46739364 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.234G>A (p.Leu78=) single nucleotide variant not specified [RCV004063244] Chr1:46258709 [GRCh38]
Chr1:46724381 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.654G>A (p.Ser218=) single nucleotide variant not specified [RCV004054389] Chr1:46260903 [GRCh38]
Chr1:46726575 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1620C>T (p.Tyr540=) single nucleotide variant not specified [RCV004057516] Chr1:46274147 [GRCh38]
Chr1:46739819 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.454G>A (p.Val152Ile) single nucleotide variant not specified [RCV004051412] Chr1:46260588 [GRCh38]
Chr1:46726260 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2050T>C (p.Cys684Arg) single nucleotide variant not specified [RCV004059647] Chr1:46278088 [GRCh38]
Chr1:46743760 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.405C>G (p.Asp135Glu) single nucleotide variant not specified [RCV004051227] Chr1:46260097 [GRCh38]
Chr1:46725769 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.599T>C (p.Leu200Pro) single nucleotide variant not specified [RCV004052541] Chr1:46260848 [GRCh38]
Chr1:46726520 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.59G>C (p.Cys20Ser) single nucleotide variant not specified [RCV004052550] Chr1:46248567 [GRCh38]
Chr1:46714239 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1467C>T (p.Ala489=) single nucleotide variant not specified [RCV004057991] Chr1:46273446 [GRCh38]
Chr1:46739118 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1656A>T (p.Arg552=) single nucleotide variant not specified [RCV004059743] Chr1:46274183 [GRCh38]
Chr1:46739855 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1048G>A (p.Ala350Thr) single nucleotide variant not specified [RCV004057406] Chr1:46270664 [GRCh38]
Chr1:46736336 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1373A>G (p.Asn458Ser) single nucleotide variant not specified [RCV004058896] Chr1:46272800 [GRCh38]
Chr1:46738472 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1351A>C (p.Thr451Pro) single nucleotide variant not specified [RCV004058793] Chr1:46272778 [GRCh38]
Chr1:46738450 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2109G>C (p.Leu703=) single nucleotide variant not specified [RCV004060355] Chr1:46278147 [GRCh38]
Chr1:46743819 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1637C>T (p.Thr546Met) single nucleotide variant not specified [RCV004058113] Chr1:46274164 [GRCh38]
Chr1:46739836 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1638G>A (p.Thr546=) single nucleotide variant not specified [RCV004058120] Chr1:46274165 [GRCh38]
Chr1:46739837 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.138T>C (p.Cys46=) single nucleotide variant not specified [RCV004057082] Chr1:46250047 [GRCh38]
Chr1:46715719 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1356G>A (p.Ser452=) single nucleotide variant not specified [RCV004058816] Chr1:46272783 [GRCh38]
Chr1:46738455 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1885G>A (p.Glu629Lys) single nucleotide variant not specified [RCV004060179] Chr1:46277832 [GRCh38]
Chr1:46743504 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1349T>C (p.Ile450Thr) single nucleotide variant not specified [RCV004058777] Chr1:46272776 [GRCh38]
Chr1:46738448 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.250G>A (p.Val84Ile) single nucleotide variant not specified [RCV004062054] Chr1:46258725 [GRCh38]
Chr1:46724397 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1101T>C (p.Ala367=) single nucleotide variant not specified [RCV004062095] Chr1:46270717 [GRCh38]
Chr1:46736389 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2195C>T (p.Thr732Ile) single nucleotide variant not specified [RCV004061185] Chr1:46278233 [GRCh38]
Chr1:46743905 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.643G>T (p.Val215Leu) single nucleotide variant not specified [RCV004053993] Chr1:46260892 [GRCh38]
Chr1:46726564 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2158C>G (p.Leu720Val) single nucleotide variant not specified [RCV004061058] Chr1:46278196 [GRCh38]
Chr1:46743868 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.6G>T (p.Arg2Ser) single nucleotide variant not specified [RCV004055130] Chr1:46248514 [GRCh38]
Chr1:46714186 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1909C>G (p.His637Asp) single nucleotide variant not specified [RCV004060812] Chr1:46277856 [GRCh38]
Chr1:46743528 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.48A>G (p.Glu16=) single nucleotide variant not specified [RCV004050180] Chr1:46248556 [GRCh38]
Chr1:46714228 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.334C>A (p.Pro112Thr) single nucleotide variant not specified [RCV004047792] Chr1:46260026 [GRCh38]
Chr1:46725698 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1761G>A (p.Arg587=) single nucleotide variant not specified [RCV004061341] Chr1:46274609 [GRCh38]
Chr1:46740281 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1642T>G (p.Ser548Ala) single nucleotide variant not specified [RCV004058147] Chr1:46274169 [GRCh38]
Chr1:46739841 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1698C>T (p.Asp566=) single nucleotide variant not specified [RCV004060494] Chr1:46274546 [GRCh38]
Chr1:46740218 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.419C>T (p.Pro140Leu) single nucleotide variant not specified [RCV004051869] Chr1:46260553 [GRCh38]
Chr1:46726225 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1050C>A (p.Ala350=) single nucleotide variant not specified [RCV004058094] Chr1:46270666 [GRCh38]
Chr1:46736338 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1363A>C (p.Lys455Gln) single nucleotide variant not specified [RCV004058850] Chr1:46272790 [GRCh38]
Chr1:46738462 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.253C>G (p.Pro85Ala) single nucleotide variant not specified [RCV004062149] Chr1:46258728 [GRCh38]
Chr1:46724400 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.274C>T (p.Pro92Ser) single nucleotide variant not specified [RCV004064101] Chr1:46259966 [GRCh38]
Chr1:46725638 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.876G>A (p.Leu292=) single nucleotide variant not specified [RCV004056694] Chr1:46261370 [GRCh38]
Chr1:46727042 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.752T>C (p.Ile251Thr) single nucleotide variant not specified [RCV004056370] Chr1:46261001 [GRCh38]
Chr1:46726673 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1569C>T (p.Thr523=) single nucleotide variant not specified [RCV004059178] Chr1:46273706 [GRCh38]
Chr1:46739378 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.704G>A (p.Gly235Glu) single nucleotide variant not specified [RCV004055189] Chr1:46260953 [GRCh38]
Chr1:46726625 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2147G>A (p.Arg716Gln) single nucleotide variant not specified [RCV004061015] Chr1:46278185 [GRCh38]
Chr1:46743857 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.254C>G (p.Pro85Arg) single nucleotide variant not specified [RCV004062186] Chr1:46258729 [GRCh38]
Chr1:46724401 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1703T>A (p.Val568Asp) single nucleotide variant not specified [RCV004060526] Chr1:46274551 [GRCh38]
Chr1:46740223 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.219T>C (p.Phe73=) single nucleotide variant not specified [RCV004061208] Chr1:46258694 [GRCh38]
Chr1:46724366 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1423G>A (p.Val475Met) single nucleotide variant not specified [RCV004057251] Chr1:46273402 [GRCh38]
Chr1:46739074 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.603A>C (p.Leu201Phe) single nucleotide variant not specified [RCV004052612] Chr1:46260852 [GRCh38]
Chr1:46726524 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1474C>T (p.Pro492Ser) single nucleotide variant not specified [RCV004058037] Chr1:46273453 [GRCh38]
Chr1:46739125 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1666G>A (p.Val556Ile) single nucleotide variant not specified [RCV004059799] Chr1:46274193 [GRCh38]
Chr1:46739865 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1666G>C (p.Val556Leu) single nucleotide variant not specified [RCV004059800] Chr1:46274193 [GRCh38]
Chr1:46739865 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1706T>C (p.Phe569Ser) single nucleotide variant not specified [RCV004060548] Chr1:46274554 [GRCh38]
Chr1:46740226 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.429G>T (p.Val143=) single nucleotide variant not specified [RCV004049948] Chr1:46260563 [GRCh38]
Chr1:46726235 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1197C>T (p.Ile399=) single nucleotide variant not specified [RCV004052254] Chr1:46272493 [GRCh38]
Chr1:46738165 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.582C>G (p.Ile194Met) single nucleotide variant not specified [RCV004054150] Chr1:46260831 [GRCh38]
Chr1:46726503 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1769T>C (p.Met590Thr) single nucleotide variant Familial cancer of breast [RCV003138254]|not specified [RCV004061380] Chr1:46274617 [GRCh38]
Chr1:46740289 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.641C>G (p.Ala214Gly) single nucleotide variant not specified [RCV004053965] Chr1:46260890 [GRCh38]
Chr1:46726562 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1051C>T (p.His351Tyr) single nucleotide variant not specified [RCV004059729] Chr1:46270667 [GRCh38]
Chr1:46736339 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1560G>A (p.Ser520=) single nucleotide variant not specified [RCV004059127] Chr1:46273697 [GRCh38]
Chr1:46739369 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.420T>C (p.Pro140=) single nucleotide variant not specified [RCV004051898] Chr1:46260554 [GRCh38]
Chr1:46726226 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.277C>T (p.Leu93=) single nucleotide variant not specified [RCV004064198] Chr1:46259969 [GRCh38]
Chr1:46725641 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.589A>G (p.Met197Val) single nucleotide variant not specified [RCV004054234] Chr1:46260838 [GRCh38]
Chr1:46726510 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1969T>A (p.Ser657Thr) single nucleotide variant not specified [RCV004061578] Chr1:46277916 [GRCh38]
Chr1:46743588 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.350C>T (p.Ala117Val) single nucleotide variant not specified [RCV004048692] Chr1:46260042 [GRCh38]
Chr1:46725714 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2206C>T (p.His736Tyr) single nucleotide variant not specified [RCV004061752] Chr1:46278244 [GRCh38]
Chr1:46743916 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2207A>C (p.His736Pro) single nucleotide variant not specified [RCV004061753] Chr1:46278245 [GRCh38]
Chr1:46743917 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.166A>G (p.Ser56Gly) single nucleotide variant not specified [RCV004059819] Chr1:46250075 [GRCh38]
Chr1:46715747 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.216A>C (p.Ala72=) single nucleotide variant not specified [RCV004061099] Chr1:46258691 [GRCh38]
Chr1:46724363 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.170A>G (p.Gln57Arg) single nucleotide variant not specified [RCV004060559] Chr1:46250079 [GRCh38]
Chr1:46715751 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.446T>G (p.Leu149Arg) single nucleotide variant not specified [RCV004050759] Chr1:46260580 [GRCh38]
Chr1:46726252 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.462G>A (p.Arg154=) single nucleotide variant not specified [RCV004051535] Chr1:46260596 [GRCh38]
Chr1:46726268 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.525C>G (p.Gly175=) single nucleotide variant not specified [RCV004052292] Chr1:46260774 [GRCh38]
Chr1:46726446 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1018C>G (p.His340Asp) single nucleotide variant not specified [RCV004599313] Chr1:46267585 [GRCh38]
Chr1:46733257 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.9G>C (p.Arg3Ser) single nucleotide variant not specified [RCV004057765] Chr1:46248517 [GRCh38]
Chr1:46714189 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1806A>C (p.Gln602His) single nucleotide variant not specified [RCV004059291] Chr1:46274654 [GRCh38]
Chr1:46740326 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1809C>T (p.Ala603=) single nucleotide variant not specified [RCV004059305] Chr1:46274657 [GRCh38]
Chr1:46740329 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1264G>C (p.Glu422Gln) single nucleotide variant not specified [RCV004056522] Chr1:46272691 [GRCh38]
Chr1:46738363 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1674C>T (p.Arg558=) single nucleotide variant not specified [RCV004059846] Chr1:46274201 [GRCh38]
Chr1:46739873 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1970C>G (p.Ser657Cys) single nucleotide variant not specified [RCV004061588] Chr1:46277917 [GRCh38]
Chr1:46743589 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1662G>A (p.Lys554=) single nucleotide variant not specified [RCV004059783] Chr1:46274189 [GRCh38]
Chr1:46739861 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1927A>G (p.Ser643Gly) single nucleotide variant not specified [RCV004060888] Chr1:46277874 [GRCh38]
Chr1:46743546 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1965C>A (p.His655Gln) single nucleotide variant not specified [RCV004061559] Chr1:46277912 [GRCh38]
Chr1:46743584 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.617A>G (p.Glu206Gly) single nucleotide variant not specified [RCV004053366] Chr1:46260866 [GRCh38]
Chr1:46726538 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.617A>T (p.Glu206Val) single nucleotide variant not specified [RCV004053368] Chr1:46260866 [GRCh38]
Chr1:46726538 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.164T>G (p.Leu55Trp) single nucleotide variant not specified [RCV004059718] Chr1:46250073 [GRCh38]
Chr1:46715745 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.104G>A (p.Arg35Gln) single nucleotide variant not specified [RCV004057528] Chr1:46250013 [GRCh38]
Chr1:46715685 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1815C>T (p.Ala605=) single nucleotide variant not specified [RCV004059345] Chr1:46274663 [GRCh38]
Chr1:46740335 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1686A>G (p.Pro562=) single nucleotide variant not specified [RCV004059903] Chr1:46274213 [GRCh38]
Chr1:46739885 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.168T>G (p.Ser56Arg) single nucleotide variant not specified [RCV004059931] Chr1:46250077 [GRCh38]
Chr1:46715749 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.925T>C (p.Tyr309His) single nucleotide variant not specified [RCV004055639] Chr1:46267492 [GRCh38]
Chr1:46733164 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.756C>T (p.Asp252=) single nucleotide variant not specified [RCV004056403] Chr1:46261005 [GRCh38]
Chr1:46726677 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1660A>G (p.Lys554Glu) single nucleotide variant not specified [RCV004059773] Chr1:46274187 [GRCh38]
Chr1:46739859 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.923C>A (p.Thr308Asn) single nucleotide variant not specified [RCV004055622] Chr1:46267490 [GRCh38]
Chr1:46733162 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.603A>G (p.Leu201=) single nucleotide variant not specified [RCV004052613] Chr1:46260852 [GRCh38]
Chr1:46726524 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.653C>T (p.Ser218Leu) single nucleotide variant not specified [RCV004054377] Chr1:46260902 [GRCh38]
Chr1:46726574 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1692C>A (p.Ser564Arg) single nucleotide variant not specified [RCV004059942] Chr1:46274540 [GRCh38]
Chr1:46740212 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1888A>G (p.Lys630Glu) single nucleotide variant not specified [RCV004060190] Chr1:46277835 [GRCh38]
Chr1:46743507 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1820T>C (p.Val607Ala) single nucleotide variant not specified [RCV004059379] Chr1:46274668 [GRCh38]
Chr1:46740340 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1822T>G (p.Trp608Gly) single nucleotide variant not specified [RCV004059385] Chr1:46274670 [GRCh38]
Chr1:46740342 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1878C>G (p.Thr626=) single nucleotide variant not specified [RCV004060147] Chr1:46277825 [GRCh38]
Chr1:46743497 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1983G>A (p.Leu661=) single nucleotide variant not specified [RCV004061650] Chr1:46277930 [GRCh38]
Chr1:46743602 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1782C>T (p.Asp594=) single nucleotide variant not specified [RCV004061452] Chr1:46274630 [GRCh38]
Chr1:46740302 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.72C>G (p.Asp24Glu) single nucleotide variant not specified [RCV004055864] Chr1:46248580 [GRCh38]
Chr1:46714252 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1978G>A (p.Glu660Lys) single nucleotide variant not specified [RCV004061627] Chr1:46277925 [GRCh38]
Chr1:46743597 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1223T>C (p.Ile408Thr) single nucleotide variant RAD54L-related disorder [RCV003933763]|not specified [RCV004054026] Chr1:46272519 [GRCh38]
Chr1:46738191 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1225G>C (p.Glu409Gln) single nucleotide variant not specified [RCV004054396] Chr1:46272521 [GRCh38]
Chr1:46738193 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.430G>A (p.Val144Ile) single nucleotide variant not specified [RCV004049971] Chr1:46260564 [GRCh38]
Chr1:46726236 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.45T>C (p.Pro15=) single nucleotide variant not specified [RCV004051496] Chr1:46248553 [GRCh38]
Chr1:46714225 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.437A>C (p.Asp146Ala) single nucleotide variant not specified [RCV004050598] Chr1:46260571 [GRCh38]
Chr1:46726243 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.784C>T (p.Arg262Cys) single nucleotide variant not specified [RCV004054726] Chr1:46261278 [GRCh38]
Chr1:46726950 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1859G>A (p.Arg620His) single nucleotide variant not specified [RCV004060054] Chr1:46274707 [GRCh38]
Chr1:46740379 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1498G>A (p.Val500Ile) single nucleotide variant not specified [RCV004058528] Chr1:46273635 [GRCh38]
Chr1:46739307 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.14T>C (p.Leu5Ser) single nucleotide variant not specified [RCV004058540] Chr1:46248522 [GRCh38]
Chr1:46714194 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2235C>T (p.Gly745=) single nucleotide variant not specified [RCV004061858] Chr1:46278273 [GRCh38]
Chr1:46743945 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1989G>A (p.Glu663=) single nucleotide variant not specified [RCV004061665] Chr1:46277936 [GRCh38]
Chr1:46743608 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.932C>A (p.Ala311Asp) single nucleotide variant not specified [RCV004055690] Chr1:46267499 [GRCh38]
Chr1:46733171 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1087A>G (p.Lys363Glu) single nucleotide variant not specified [RCV004061798] Chr1:46270703 [GRCh38]
Chr1:46736375 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.424C>T (p.His142Tyr) single nucleotide variant not specified [RCV004049839] Chr1:46260558 [GRCh38]
Chr1:46726230 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1063A>G (p.Lys355Glu) single nucleotide variant not specified [RCV004059413] Chr1:46270679 [GRCh38]
Chr1:46736351 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1688C>T (p.Ser563Leu) single nucleotide variant not specified [RCV004059916] Chr1:46274215 [GRCh38]
Chr1:46739887 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2106C>T (p.Asp702=) single nucleotide variant not specified [RCV004060342] Chr1:46278144 [GRCh38]
Chr1:46743816 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.144G>T (p.Leu48=) single nucleotide variant RAD54L-related disorder [RCV003943390]|not specified [RCV004057903] Chr1:46250053 [GRCh38]
Chr1:46715725 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1091G>A (p.Gly364Asp) single nucleotide variant not specified [RCV004062659] Chr1:46270707 [GRCh38]
Chr1:46736379 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1616T>C (p.Leu539Ser) single nucleotide variant not specified [RCV004057493] Chr1:46274143 [GRCh38]
Chr1:46739815 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.22A>C (p.Ser8Arg) single nucleotide variant not specified [RCV004062610] Chr1:46248530 [GRCh38]
Chr1:46714202 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2108T>C (p.Leu703Pro) single nucleotide variant not specified [RCV004060348] Chr1:46278146 [GRCh38]
Chr1:46743818 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.689T>C (p.Val230Ala) single nucleotide variant not specified [RCV004052938] Chr1:46260938 [GRCh38]
Chr1:46726610 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1040T>G (p.Leu347Arg) single nucleotide variant not specified [RCV004058556] Chr1:46267607 [GRCh38]
Chr1:46733279 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2100T>C (p.Thr700=) single nucleotide variant not specified [RCV004060325] Chr1:46278138 [GRCh38]
Chr1:46743810 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1907G>C (p.Ser636Thr) single nucleotide variant not specified [RCV004060799] Chr1:46277854 [GRCh38]
Chr1:46743526 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1910A>C (p.His637Pro) single nucleotide variant not specified [RCV004060817] Chr1:46277857 [GRCh38]
Chr1:46743529 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1910A>G (p.His637Arg) single nucleotide variant not specified [RCV004060818] Chr1:46277857 [GRCh38]
Chr1:46743529 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1252C>G (p.Pro418Ala) single nucleotide variant not specified [RCV004054749] Chr1:46272679 [GRCh38]
Chr1:46738351 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.279G>A (p.Leu93=) single nucleotide variant not specified [RCV004062241] Chr1:46259971 [GRCh38]
Chr1:46725643 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1623C>T (p.Val541=) single nucleotide variant not specified [RCV004057526] Chr1:46274150 [GRCh38]
Chr1:46739822 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.336C>G (p.Pro112=) single nucleotide variant not specified [RCV004047853] Chr1:46260028 [GRCh38]
Chr1:46725700 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1155C>T (p.Thr385=) single nucleotide variant not specified [RCV004048132] Chr1:46270771 [GRCh38]
Chr1:46736443 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.380G>A (p.Ser127Asn) single nucleotide variant not specified [RCV004048135] Chr1:46260072 [GRCh38]
Chr1:46725744 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.116G>A (p.Ser39Asn) single nucleotide variant not specified [RCV004049869] Chr1:46250025 [GRCh38]
Chr1:46715697 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.461G>A (p.Arg154Gln) single nucleotide variant not specified [RCV004051521] Chr1:46260595 [GRCh38]
Chr1:46726267 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1914G>A (p.Lys638=) single nucleotide variant not specified [RCV004060834] Chr1:46277861 [GRCh38]
Chr1:46743533 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1866G>C (p.Leu622=) single nucleotide variant not specified [RCV004060083] Chr1:46274714 [GRCh38]
Chr1:46740386 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.978T>C (p.Thr326=) single nucleotide variant not specified [RCV004057610] Chr1:46267545 [GRCh38]
Chr1:46733217 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1641G>C (p.Met547Ile) single nucleotide variant Familial cancer of breast [RCV004584974]|not specified [RCV004058143] Chr1:46274168 [GRCh38]
Chr1:46739840 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.342A>G (p.Glu114=) single nucleotide variant not specified [RCV004047996] Chr1:46260034 [GRCh38]
Chr1:46725706 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1362G>A (p.Lys454=) single nucleotide variant not specified [RCV004058847] Chr1:46272789 [GRCh38]
Chr1:46738461 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.807C>T (p.Pro269=) single nucleotide variant not specified [RCV004055425] Chr1:46261301 [GRCh38]
Chr1:46726973 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.826G>A (p.Glu276Lys) single nucleotide variant not specified [RCV004055586] Chr1:46261320 [GRCh38]
Chr1:46726992 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.746A>T (p.Asp249Val) single nucleotide variant not specified [RCV004056303] Chr1:46260995 [GRCh38]
Chr1:46726667 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1747A>T (p.Ile583Phe) single nucleotide variant not specified [RCV004061266] Chr1:46274595 [GRCh38]
Chr1:46740267 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.433G>C (p.Val145Leu) single nucleotide variant not specified [RCV004050020] Chr1:46260567 [GRCh38]
Chr1:46726239 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1875G>C (p.Gly625=) single nucleotide variant not specified [RCV004060130] Chr1:46277822 [GRCh38]
Chr1:46743494 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1876A>G (p.Thr626Ala) single nucleotide variant not specified [RCV004060134] Chr1:46277823 [GRCh38]
Chr1:46743495 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1877C>T (p.Thr626Ile) single nucleotide variant not specified [RCV004060144] Chr1:46277824 [GRCh38]
Chr1:46743496 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.570G>A (p.Thr190=) single nucleotide variant not specified [RCV004053736] Chr1:46260819 [GRCh38]
Chr1:46726491 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1416T>A (p.Asp472Glu) single nucleotide variant not specified [RCV004057209] Chr1:46273395 [GRCh38]
Chr1:46739067 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1209T>C (p.Tyr403=) single nucleotide variant not specified [RCV004054090] Chr1:46272505 [GRCh38]
Chr1:46738177 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.325C>A (p.Leu109Ile) single nucleotide variant not specified [RCV004049378] Chr1:46260017 [GRCh38]
Chr1:46725689 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1143G>C (p.Leu381=) single nucleotide variant not specified [RCV004048646] Chr1:46270759 [GRCh38]
Chr1:46736431 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.294G>A (p.Leu98=) single nucleotide variant not specified [RCV004065325] Chr1:46259986 [GRCh38]
Chr1:46725658 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1241G>A (p.Cys414Tyr) single nucleotide variant not specified [RCV004055920] Chr1:46272537 [GRCh38]
Chr1:46738209 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.347A>G (p.Asp116Gly) single nucleotide variant not specified [RCV004048617] Chr1:46260039 [GRCh38]
Chr1:46725711 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.117T>C (p.Ser39=) single nucleotide variant not specified [RCV004051518] Chr1:46250026 [GRCh38]
Chr1:46715698 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.492G>T (p.Leu164=) single nucleotide variant RAD54L-related disorder [RCV003926375]|not specified [RCV004050243] Chr1:46260741 [GRCh38]
Chr1:46726413 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1834C>G (p.Gln612Glu) single nucleotide variant not specified [RCV004059435] Chr1:46274682 [GRCh38]
Chr1:46740354 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1602T>G (p.Arg534=) single nucleotide variant not specified [RCV004057428] Chr1:46273739 [GRCh38]
Chr1:46739411 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.374C>T (p.Pro125Leu) single nucleotide variant not specified [RCV004048005] Chr1:46260066 [GRCh38]
Chr1:46725738 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.562G>A (p.Gly188Arg) single nucleotide variant not specified [RCV004053629] Chr1:46260811 [GRCh38]
Chr1:46726483 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1128A>T (p.Leu376=) single nucleotide variant not specified [RCV004048263] Chr1:46270744 [GRCh38]
Chr1:46736416 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1557G>A (p.Val519=) single nucleotide variant not specified [RCV004059101] Chr1:46273694 [GRCh38]
Chr1:46739366 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1559C>T (p.Ser520Leu) single nucleotide variant Familial cancer of breast [RCV003340489]|not specified [RCV004059112] Chr1:46273696 [GRCh38]
Chr1:46739368 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1923G>A (p.Leu641=) single nucleotide variant not specified [RCV004060874] Chr1:46277870 [GRCh38]
Chr1:46743542 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.494G>C (p.Trp165Ser) single nucleotide variant not specified [RCV004050275] Chr1:46260743 [GRCh38]
Chr1:46726415 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.494G>T (p.Trp165Leu) single nucleotide variant not specified [RCV004050276] Chr1:46260743 [GRCh38]
Chr1:46726415 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1703T>C (p.Val568Ala) single nucleotide variant not specified [RCV004060527] Chr1:46274551 [GRCh38]
Chr1:46740223 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2202C>G (p.Val734=) single nucleotide variant not specified [RCV004061736] Chr1:46278240 [GRCh38]
Chr1:46743912 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1216G>A (p.Val406Met) single nucleotide variant not specified [RCV004053275] Chr1:46272512 [GRCh38]
Chr1:46738184 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.612T>G (p.Ser204Arg) single nucleotide variant not specified [RCV004053296] Chr1:46260861 [GRCh38]
Chr1:46726533 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1858C>T (p.Arg620Cys) single nucleotide variant not specified [RCV004060051] Chr1:46274706 [GRCh38]
Chr1:46740378 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2203T>A (p.Phe735Ile) single nucleotide variant not specified [RCV004061743] Chr1:46278241 [GRCh38]
Chr1:46743913 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2163G>A (p.Gln721=) single nucleotide variant not specified [RCV004061082] Chr1:46278201 [GRCh38]
Chr1:46743873 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.375G>T (p.Pro125=) single nucleotide variant not specified [RCV004048031] Chr1:46260067 [GRCh38]
Chr1:46725739 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.579C>T (p.Cys193=) single nucleotide variant not specified [RCV004054098] Chr1:46260828 [GRCh38]
Chr1:46726500 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.55T>C (p.Ser19Pro) single nucleotide variant not specified [RCV004053580] Chr1:46248563 [GRCh38]
Chr1:46714235 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1431C>T (p.Ala477=) single nucleotide variant not specified [RCV004057806] Chr1:46273410 [GRCh38]
Chr1:46739082 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.467A>G (p.His156Arg) single nucleotide variant not specified [RCV004051964] Chr1:46260601 [GRCh38]
Chr1:46726273 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.866G>C (p.Ser289Thr) single nucleotide variant not specified [RCV004056610] Chr1:46261360 [GRCh38]
Chr1:46727032 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2208C>T (p.His736=) single nucleotide variant not specified [RCV004061759] Chr1:46278246 [GRCh38]
Chr1:46743918 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1215T>C (p.Pro405=) single nucleotide variant not specified [RCV004052707] Chr1:46272511 [GRCh38]
Chr1:46738183 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1298C>T (p.Pro433Leu) single nucleotide variant not specified [RCV004058227] Chr1:46272725 [GRCh38]
Chr1:46738397 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.375G>A (p.Pro125=) single nucleotide variant not specified [RCV004048027] Chr1:46260067 [GRCh38]
Chr1:46725739 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.446T>C (p.Leu149Pro) single nucleotide variant not specified [RCV004050758] Chr1:46260580 [GRCh38]
Chr1:46726252 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1933G>A (p.Val645Met) single nucleotide variant not specified [RCV004060920] Chr1:46277880 [GRCh38]
Chr1:46743552 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1848C>T (p.Cys616=) single nucleotide variant not specified [RCV004060011] Chr1:46274696 [GRCh38]
Chr1:46740368 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.184C>A (p.Pro62Thr) single nucleotide variant not specified [RCV004060019] Chr1:46250093 [GRCh38]
Chr1:46715765 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1850A>G (p.Tyr617Cys) single nucleotide variant not specified [RCV004060022] Chr1:46274698 [GRCh38]
Chr1:46740370 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1230G>A (p.Gln410=) single nucleotide variant not specified [RCV004052807] Chr1:46272526 [GRCh38]
Chr1:46738198 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.360G>A (p.Leu120=) single nucleotide variant not specified [RCV004049238] Chr1:46260052 [GRCh38]
Chr1:46725724 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2058C>T (p.Asn686=) single nucleotide variant not specified [RCV004059666] Chr1:46278096 [GRCh38]
Chr1:46743768 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2059A>G (p.Ser687Gly) single nucleotide variant not specified [RCV004059669] Chr1:46278097 [GRCh38]
Chr1:46743769 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1536C>T (p.Ser512=) single nucleotide variant not specified [RCV004058986] Chr1:46273673 [GRCh38]
Chr1:46739345 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2058C>A (p.Asn686Lys) single nucleotide variant not specified [RCV004059664] Chr1:46278096 [GRCh38]
Chr1:46743768 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2216C>T (p.Ser739Phe) single nucleotide variant not specified [RCV004061785] Chr1:46278254 [GRCh38]
Chr1:46743926 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1934T>G (p.Val645Gly) single nucleotide variant not specified [RCV004060922] Chr1:46277881 [GRCh38]
Chr1:46743553 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1938G>T (p.Val646=) single nucleotide variant not specified [RCV004060943] Chr1:46277885 [GRCh38]
Chr1:46743557 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1852A>G (p.Ile618Val) single nucleotide variant not specified [RCV004060031] Chr1:46274700 [GRCh38]
Chr1:46740372 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1231G>A (p.Val411Ile) single nucleotide variant not specified [RCV004052851] Chr1:46272527 [GRCh38]
Chr1:46738199 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1526G>A (p.Arg509Gln) single nucleotide variant not specified [RCV004058682] Chr1:46273663 [GRCh38]
Chr1:46739335 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1533T>G (p.Arg511=) single nucleotide variant not specified [RCV004058977] Chr1:46273670 [GRCh38]
Chr1:46739342 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1044G>T (p.Gly348=) single nucleotide variant not specified [RCV004059072] Chr1:46270660 [GRCh38]
Chr1:46736332 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.516C>T (p.Arg172=) single nucleotide variant not specified [RCV004051630] Chr1:46260765 [GRCh38]
Chr1:46726437 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.779A>G (p.Asn260Ser) single nucleotide variant not specified [RCV004054688] Chr1:46261273 [GRCh38]
Chr1:46726945 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1352C>T (p.Thr451Ile) single nucleotide variant not specified [RCV004599342] Chr1:46272779 [GRCh38]
Chr1:46738451 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1523C>A (p.Thr508Asn) single nucleotide variant not specified [RCV004058666] Chr1:46273660 [GRCh38]
Chr1:46739332 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.828G>A (p.Glu276=) single nucleotide variant not specified [RCV004056006] Chr1:46261322 [GRCh38]
Chr1:46726994 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1078C>G (p.Pro360Ala) single nucleotide variant not specified [RCV004060228] Chr1:46270694 [GRCh38]
Chr1:46736366 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1181G>A (p.Arg394Gln) single nucleotide variant not specified [RCV004051611] Chr1:46272477 [GRCh38]
Chr1:46738149 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.171G>A (p.Gln57=) single nucleotide variant not specified [RCV004060613] Chr1:46250080 [GRCh38]
Chr1:46715752 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.193C>T (p.Leu65=) single nucleotide variant not specified [RCV004060948] Chr1:46250102 [GRCh38]
Chr1:46715774 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1941T>A (p.Asp647Glu) single nucleotide variant not specified [RCV004060957] Chr1:46277888 [GRCh38]
Chr1:46743560 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1941T>C (p.Asp647=) single nucleotide variant not specified [RCV004060959] Chr1:46277888 [GRCh38]
Chr1:46743560 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1944G>A (p.Glu648=) single nucleotide variant not specified [RCV004060975] Chr1:46277891 [GRCh38]
Chr1:46743563 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2080C>G (p.Pro694Ala) single nucleotide variant not specified [RCV004060261] Chr1:46278118 [GRCh38]
Chr1:46743790 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1606C>G (p.Arg536Gly) single nucleotide variant not specified [RCV004057445] Chr1:46273743 [GRCh38]
Chr1:46739415 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1814C>T (p.Ala605Val) single nucleotide variant not specified [RCV004059340] Chr1:46274662 [GRCh38]
Chr1:46740334 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.274C>A (p.Pro92Thr) single nucleotide variant not specified [RCV004599402] Chr1:46259966 [GRCh38]
Chr1:46725638 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.942C>T (p.Ser314=) single nucleotide variant not specified [RCV004056794] Chr1:46267509 [GRCh38]
Chr1:46733181 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.943T>C (p.Leu315=) single nucleotide variant not specified [RCV004056805] Chr1:46267510 [GRCh38]
Chr1:46733182 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.945G>A (p.Leu315=) single nucleotide variant not specified [RCV004056829] Chr1:46267512 [GRCh38]
Chr1:46733184 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2137T>C (p.Trp713Arg) single nucleotide variant not specified [RCV004060467] Chr1:46278175 [GRCh38]
Chr1:46743847 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2075C>T (p.Pro692Leu) single nucleotide variant not specified [RCV004060236] Chr1:46278113 [GRCh38]
Chr1:46743785 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1279T>G (p.Phe427Val) single nucleotide variant not specified [RCV004056924] Chr1:46272706 [GRCh38]
Chr1:46738378 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.261A>T (p.Pro87=) single nucleotide variant not specified [RCV004062959] Chr1:46258736 [GRCh38]
Chr1:46724408 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1547T>C (p.Val516Ala) single nucleotide variant not specified [RCV004059046] Chr1:46273684 [GRCh38]
Chr1:46739356 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.82G>A (p.Gly28Ser) single nucleotide variant not specified [RCV004056019] Chr1:46248590 [GRCh38]
Chr1:46714262 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1378C>T (p.Pro460Ser) single nucleotide variant not specified [RCV004058925] Chr1:46273357 [GRCh38]
Chr1:46739029 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.994C>T (p.Leu332=) single nucleotide variant not specified [RCV004057715] Chr1:46267561 [GRCh38]
Chr1:46733233 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.775A>G (p.Met259Val) single nucleotide variant not specified [RCV004054648] Chr1:46261269 [GRCh38]
Chr1:46726941 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.718C>T (p.Pro240Ser) single nucleotide variant not specified [RCV004055736] Chr1:46260967 [GRCh38]
Chr1:46726639 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.584C>T (p.Thr195Ile) single nucleotide variant not specified [RCV004054189] Chr1:46260833 [GRCh38]
Chr1:46726505 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2144T>C (p.Leu715Pro) single nucleotide variant not specified [RCV004061005] Chr1:46278182 [GRCh38]
Chr1:46743854 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1818G>A (p.Arg606=) single nucleotide variant not specified [RCV004059358] Chr1:46274666 [GRCh38]
Chr1:46740338 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.403G>T (p.Asp135Tyr) single nucleotide variant not specified [RCV004051184] Chr1:46260095 [GRCh38]
Chr1:46725767 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.903C>T (p.Leu301=) single nucleotide variant not specified [RCV004054944] Chr1:46267470 [GRCh38]
Chr1:46733142 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1389C>T (p.Ile463=) single nucleotide variant not specified [RCV004057070] Chr1:46273368 [GRCh38]
Chr1:46739040 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.719C>T (p.Pro240Leu) single nucleotide variant not specified [RCV004055741] Chr1:46260968 [GRCh38]
Chr1:46726640 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1384C>T (p.Leu462=) single nucleotide variant not specified [RCV004057038] Chr1:46273363 [GRCh38]
Chr1:46739035 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.781C>A (p.Gln261Lys) single nucleotide variant not specified [RCV004054709] Chr1:46261275 [GRCh38]
Chr1:46726947 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.368C>T (p.Pro123Leu) single nucleotide variant not specified [RCV004049675] Chr1:46260060 [GRCh38]
Chr1:46725732 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1655G>A (p.Arg552Gln) single nucleotide variant not specified [RCV004059740] Chr1:46274182 [GRCh38]
Chr1:46739854 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1469T>C (p.Leu490Pro) single nucleotide variant not specified [RCV004057999] Chr1:46273448 [GRCh38]
Chr1:46739120 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1014G>A (p.Leu338=) single nucleotide variant not specified [RCV004050007] Chr1:46267581 [GRCh38]
Chr1:46733253 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2146C>A (p.Arg716=) single nucleotide variant not specified [RCV004061009] Chr1:46278184 [GRCh38]
Chr1:46743856 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1652A>C (p.Lys551Thr) single nucleotide variant not specified [RCV004059730] Chr1:46274179 [GRCh38]
Chr1:46739851 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1398G>A (p.Lys466=) single nucleotide variant not specified [RCV004057116] Chr1:46273377 [GRCh38]
Chr1:46739049 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.944T>G (p.Leu315Trp) single nucleotide variant not specified [RCV004056817] Chr1:46267511 [GRCh38]
Chr1:46733183 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.651G>A (p.Val217=) single nucleotide variant not specified [RCV004054353] Chr1:46260900 [GRCh38]
Chr1:46726572 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1381G>C (p.Ala461Pro) single nucleotide variant not specified [RCV004057025] Chr1:46273360 [GRCh38]
Chr1:46739032 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.134A>G (p.Glu45Gly) single nucleotide variant not specified [RCV004119293] Chr1:46250043 [GRCh38]
Chr1:46715715 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2138G>T (p.Trp713Leu) single nucleotide variant not specified [RCV004231304] Chr1:46278176 [GRCh38]
Chr1:46743848 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.770G>T (p.Gly257Val) single nucleotide variant not specified [RCV004233392] Chr1:46261264 [GRCh38]
Chr1:46726936 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1621G>A (p.Val541Ile) single nucleotide variant not specified [RCV004226900] Chr1:46274148 [GRCh38]
Chr1:46739820 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2200G>A (p.Val734Ile) single nucleotide variant not specified [RCV004209085] Chr1:46278238 [GRCh38]
Chr1:46743910 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1250C>T (p.Thr417Ile) single nucleotide variant Familial cancer of breast [RCV003154093]|not specified [RCV004246179] Chr1:46272677 [GRCh38]
Chr1:46738349 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.399G>A (p.Lys133=) single nucleotide variant not specified [RCV004327934] Chr1:46260091 [GRCh38]
Chr1:46725763 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.561A>G (p.Leu187=) single nucleotide variant not specified [RCV004327937] Chr1:46260810 [GRCh38]
Chr1:46726482 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1813G>A (p.Ala605Thr) single nucleotide variant not specified [RCV004330311] Chr1:46274661 [GRCh38]
Chr1:46740333 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1716C>T (p.Ser572=) single nucleotide variant not specified [RCV004330312] Chr1:46274564 [GRCh38]
Chr1:46740236 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.327C>T (p.Leu109=) single nucleotide variant not specified [RCV004330313] Chr1:46260019 [GRCh38]
Chr1:46725691 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2091T>C (p.Ser697=) single nucleotide variant not specified [RCV004330317] Chr1:46278129 [GRCh38]
Chr1:46743801 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1519G>A (p.Val507Met) single nucleotide variant not specified [RCV004330318] Chr1:46273656 [GRCh38]
Chr1:46739328 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1951G>T (p.Asp651Tyr) single nucleotide variant not specified [RCV004330332] Chr1:46277898 [GRCh38]
Chr1:46743570 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1428T>C (p.Gly476=) single nucleotide variant not specified [RCV004330334] Chr1:46273407 [GRCh38]
Chr1:46739079 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1812G>A (p.Met604Ile) single nucleotide variant not specified [RCV004327923] Chr1:46274660 [GRCh38]
Chr1:46740332 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.915G>A (p.Glu305=) single nucleotide variant not specified [RCV004262925] Chr1:46267482 [GRCh38]
Chr1:46733154 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1518G>T (p.Ala506=) single nucleotide variant not specified [RCV004262839] Chr1:46273655 [GRCh38]
Chr1:46739327 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.525C>T (p.Gly175=) single nucleotide variant not specified [RCV004256181] Chr1:46260774 [GRCh38]
Chr1:46726446 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2080C>T (p.Pro694Ser) single nucleotide variant not specified [RCV004260348] Chr1:46278118 [GRCh38]
Chr1:46743790 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.224G>A (p.Arg75Gln) single nucleotide variant not specified [RCV004258388] Chr1:46258699 [GRCh38]
Chr1:46724371 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1737C>T (p.Gly579=) single nucleotide variant not specified [RCV004281402] Chr1:46274585 [GRCh38]
Chr1:46740257 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2182T>C (p.Ser728Pro) single nucleotide variant not specified [RCV004281403] Chr1:46278220 [GRCh38]
Chr1:46743892 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.177C>G (p.Thr59=) single nucleotide variant not specified [RCV004247418] Chr1:46250086 [GRCh38]
Chr1:46715758 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1846T>C (p.Cys616Arg) single nucleotide variant not specified [RCV004247421] Chr1:46274694 [GRCh38]
Chr1:46740366 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.316C>T (p.Arg106Cys) single nucleotide variant not specified [RCV004252682] Chr1:46260008 [GRCh38]
Chr1:46725680 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.440C>G (p.Pro147Arg) single nucleotide variant not specified [RCV004260609] Chr1:46260574 [GRCh38]
Chr1:46726246 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1679A>G (p.Asn560Ser) single nucleotide variant not specified [RCV004257802] Chr1:46274206 [GRCh38]
Chr1:46739878 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.713T>C (p.Ile238Thr) single nucleotide variant not specified [RCV004247427] Chr1:46260962 [GRCh38]
Chr1:46726634 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2217T>C (p.Ser739=) single nucleotide variant not specified [RCV004247426] Chr1:46278255 [GRCh38]
Chr1:46743927 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.499T>G (p.Cys167Gly) single nucleotide variant not specified [RCV004247420] Chr1:46260748 [GRCh38]
Chr1:46726420 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1379C>T (p.Pro460Leu) single nucleotide variant not specified [RCV004260750] Chr1:46273358 [GRCh38]
Chr1:46739030 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.883T>C (p.Cys295Arg) single nucleotide variant not provided [RCV003491344]|not specified [RCV004258064] Chr1:46261377 [GRCh38]
Chr1:46727049 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.686A>T (p.Glu229Val) single nucleotide variant not specified [RCV004255774] Chr1:46260935 [GRCh38]
Chr1:46726607 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1180C>T (p.Arg394Trp) single nucleotide variant not specified [RCV004260272] Chr1:46272476 [GRCh38]
Chr1:46738148 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1094G>C (p.Arg365Pro) single nucleotide variant not specified [RCV004247425] Chr1:46270710 [GRCh38]
Chr1:46736382 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1771T>C (p.Phe591Leu) single nucleotide variant not specified [RCV004247423] Chr1:46274619 [GRCh38]
Chr1:46740291 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1950G>C (p.Gln650His) single nucleotide variant not specified [RCV004247422] Chr1:46277897 [GRCh38]
Chr1:46743569 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1768A>G (p.Met590Val) single nucleotide variant not specified [RCV004247416] Chr1:46274616 [GRCh38]
Chr1:46740288 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.281G>C (p.Gly94Ala) single nucleotide variant not specified [RCV004252903] Chr1:46259973 [GRCh38]
Chr1:46725645 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.86T>C (p.Leu29Pro) single nucleotide variant not specified [RCV004262561] Chr1:46248594 [GRCh38]
Chr1:46714266 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.473G>C (p.Arg158Thr) single nucleotide variant not specified [RCV004262729] Chr1:46260607 [GRCh38]
Chr1:46726279 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1016T>C (p.Val339Ala) single nucleotide variant not specified [RCV004256017] Chr1:46267583 [GRCh38]
Chr1:46733255 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.396G>C (p.Leu132=) single nucleotide variant not specified [RCV004258549] Chr1:46260088 [GRCh38]
Chr1:46725760 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2129C>G (p.Thr710Ser) single nucleotide variant not specified [RCV004262290] Chr1:46278167 [GRCh38]
Chr1:46743839 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.9G>A (p.Arg3=) single nucleotide variant not specified [RCV004256104] Chr1:46248517 [GRCh38]
Chr1:46714189 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1479G>C (p.Gln493His) single nucleotide variant not specified [RCV004247419] Chr1:46273458 [GRCh38]
Chr1:46739130 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1617A>T (p.Leu539Phe) single nucleotide variant not specified [RCV004247431] Chr1:46274144 [GRCh38]
Chr1:46739816 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2047C>T (p.Arg683Cys) single nucleotide variant not specified [RCV004260162] Chr1:46278085 [GRCh38]
Chr1:46743757 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.265T>C (p.Tyr89His) single nucleotide variant not specified [RCV004281407] Chr1:46258740 [GRCh38]
Chr1:46724412 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.906G>A (p.Lys302=) single nucleotide variant not specified [RCV004261010] Chr1:46267473 [GRCh38]
Chr1:46733145 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.836G>A (p.Arg279His) single nucleotide variant not specified [RCV004253922] Chr1:46261330 [GRCh38]
Chr1:46727002 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.955C>T (p.Arg319Trp) single nucleotide variant not specified [RCV004257906] Chr1:46267522 [GRCh38]
Chr1:46733194 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.384T>A (p.Ala128=) single nucleotide variant not specified [RCV004247449] Chr1:46260076 [GRCh38]
Chr1:46725748 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.137G>A (p.Cys46Tyr) single nucleotide variant not specified [RCV004247445] Chr1:46250046 [GRCh38]
Chr1:46715718 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1895T>G (p.Phe632Cys) single nucleotide variant not specified [RCV004247444] Chr1:46277842 [GRCh38]
Chr1:46743514 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1120A>G (p.Arg374Gly) single nucleotide variant not specified [RCV004247434] Chr1:46270736 [GRCh38]
Chr1:46736408 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1665T>G (p.Val555=) single nucleotide variant not specified [RCV004247433] Chr1:46274192 [GRCh38]
Chr1:46739864 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.247A>G (p.Lys83Glu) single nucleotide variant not specified [RCV004247430] Chr1:46258722 [GRCh38]
Chr1:46724394 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.319C>T (p.Arg107Trp) single nucleotide variant not specified [RCV004258159] Chr1:46260011 [GRCh38]
Chr1:46725683 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.788G>A (p.Gly263Glu) single nucleotide variant not specified [RCV004260075] Chr1:46261282 [GRCh38]
Chr1:46726954 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.785G>T (p.Arg262Leu) single nucleotide variant not specified [RCV004262367] Chr1:46261279 [GRCh38]
Chr1:46726951 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1234G>T (p.Val412Phe) single nucleotide variant not specified [RCV004263024] Chr1:46272530 [GRCh38]
Chr1:46738202 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1333T>A (p.Ser445Thr) single nucleotide variant not specified [RCV004256506] Chr1:46272760 [GRCh38]
Chr1:46738432 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.535T>A (p.Cys179Ser) single nucleotide variant not specified [RCV004256425] Chr1:46260784 [GRCh38]
Chr1:46726456 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.122C>T (p.Thr41Ile) single nucleotide variant not specified [RCV004258718] Chr1:46250031 [GRCh38]
Chr1:46715703 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.214G>C (p.Ala72Pro) single nucleotide variant Familial cancer of breast [RCV003142329] Chr1:46258689 [GRCh38]
Chr1:46724361 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1811T>C (p.Met604Thr) single nucleotide variant not specified [RCV004258801] Chr1:46274659 [GRCh38]
Chr1:46740331 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.180T>C (p.Asn60=) single nucleotide variant not specified [RCV004258884] Chr1:46250089 [GRCh38]
Chr1:46715761 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.816C>G (p.Ile272Met) single nucleotide variant not specified [RCV004263098] Chr1:46261310 [GRCh38]
Chr1:46726982 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.683A>G (p.Asn228Ser) single nucleotide variant not specified [RCV004255836] Chr1:46260932 [GRCh38]
Chr1:46726604 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.320G>A (p.Arg107Gln) single nucleotide variant not specified [RCV004255614] Chr1:46260012 [GRCh38]
Chr1:46725684 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.954C>G (p.Ser318Arg) single nucleotide variant not specified [RCV004255694] Chr1:46267521 [GRCh38]
Chr1:46733193 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1336T>A (p.Ser446Thr) single nucleotide variant not specified [RCV004257989] Chr1:46272763 [GRCh38]
Chr1:46738435 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1520T>C (p.Val507Ala) single nucleotide variant not specified [RCV004258239] Chr1:46273657 [GRCh38]
Chr1:46739329 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1360A>G (p.Lys454Glu) single nucleotide variant not specified [RCV004258636] Chr1:46272787 [GRCh38]
Chr1:46738459 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.333C>T (p.Asp111=) single nucleotide variant not specified [RCV004260528] Chr1:46260025 [GRCh38]
Chr1:46725697 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1788C>G (p.Asn596Lys) single nucleotide variant not specified [RCV004260450] Chr1:46274636 [GRCh38]
Chr1:46740308 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.835C>T (p.Arg279Cys) single nucleotide variant not specified [RCV004262449] Chr1:46261329 [GRCh38]
Chr1:46727001 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1777C>A (p.Pro593Thr) single nucleotide variant not specified [RCV004260195] Chr1:46274625 [GRCh38]
Chr1:46740297 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.28C>G (p.Leu10Val) single nucleotide variant not specified [RCV004262817] Chr1:46248536 [GRCh38]
Chr1:46714208 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.136T>G (p.Cys46Gly) single nucleotide variant not specified [RCV004258472] Chr1:46250045 [GRCh38]
Chr1:46715717 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1944G>C (p.Glu648Asp) single nucleotide variant not specified [RCV004259921] Chr1:46277891 [GRCh38]
Chr1:46743563 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2082T>C (p.Pro694=) single nucleotide variant not specified [RCV004260825] Chr1:46278120 [GRCh38]
Chr1:46743792 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.54G>T (p.Arg18Ser) single nucleotide variant not specified [RCV004247446] Chr1:46248562 [GRCh38]
Chr1:46714234 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1702G>T (p.Val568Phe) single nucleotide variant not specified [RCV004247448] Chr1:46274550 [GRCh38]
Chr1:46740222 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1538G>A (p.Ser513Asn) single nucleotide variant not specified [RCV004247428] Chr1:46273675 [GRCh38]
Chr1:46739347 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2080C>A (p.Pro694Thr) single nucleotide variant not specified [RCV004258628] Chr1:46278118 [GRCh38]
Chr1:46743790 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2072G>A (p.Arg691Gln) single nucleotide variant not specified [RCV004259997] Chr1:46278110 [GRCh38]
Chr1:46743782 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.111C>T (p.Ser37=) single nucleotide variant not specified [RCV004281401] Chr1:46250020 [GRCh38]
Chr1:46715692 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.358C>T (p.Leu120=) single nucleotide variant not specified [RCV004281404] Chr1:46260050 [GRCh38]
Chr1:46725722 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1260G>T (p.Gln420His) single nucleotide variant not specified [RCV004281405] Chr1:46272687 [GRCh38]
Chr1:46738359 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.506C>T (p.Thr169Ile) single nucleotide variant not specified [RCV004281406] Chr1:46260755 [GRCh38]
Chr1:46726427 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.565A>G (p.Lys189Glu) single nucleotide variant not specified [RCV004281409] Chr1:46260814 [GRCh38]
Chr1:46726486 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2204T>C (p.Phe735Ser) single nucleotide variant not specified [RCV004281410] Chr1:46278242 [GRCh38]
Chr1:46743914 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.838C>T (p.Leu280Phe) single nucleotide variant not specified [RCV004281411] Chr1:46261332 [GRCh38]
Chr1:46727004 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.609G>T (p.Gln203His) single nucleotide variant not specified [RCV004262651] Chr1:46260858 [GRCh38]
Chr1:46726530 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1145G>A (p.Arg382Gln) single nucleotide variant not specified [RCV004255932] Chr1:46270761 [GRCh38]
Chr1:46736433 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.246C>G (p.Phe82Leu) single nucleotide variant not specified [RCV004247417] Chr1:46258721 [GRCh38]
Chr1:46724393 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1499T>A (p.Val500Asp) single nucleotide variant not specified [RCV004247424] Chr1:46273636 [GRCh38]
Chr1:46739308 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1743T>C (p.Asn581=) single nucleotide variant not specified [RCV004247429] Chr1:46274591 [GRCh38]
Chr1:46740263 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.796G>A (p.Val266Met) single nucleotide variant not specified [RCV004247432] Chr1:46261290 [GRCh38]
Chr1:46726962 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.829A>T (p.Thr277Ser) single nucleotide variant not specified [RCV004247435] Chr1:46261323 [GRCh38]
Chr1:46726995 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1430C>T (p.Ala477Val) single nucleotide variant not specified [RCV004247436] Chr1:46273409 [GRCh38]
Chr1:46739081 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1505A>G (p.Asp502Gly) single nucleotide variant not specified [RCV004247437] Chr1:46273642 [GRCh38]
Chr1:46739314 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1736G>A (p.Gly579Asp) single nucleotide variant not specified [RCV004247438] Chr1:46274584 [GRCh38]
Chr1:46740256 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1140G>C (p.Arg380=) single nucleotide variant not specified [RCV004247439] Chr1:46270756 [GRCh38]
Chr1:46736428 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1505A>C (p.Asp502Ala) single nucleotide variant not specified [RCV004247440] Chr1:46273642 [GRCh38]
Chr1:46739314 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1292C>G (p.Ala431Gly) single nucleotide variant not specified [RCV004247441] Chr1:46272719 [GRCh38]
Chr1:46738391 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1442T>C (p.Phe481Ser) single nucleotide variant not specified [RCV004247442] Chr1:46273421 [GRCh38]
Chr1:46739093 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1814C>A (p.Ala605Asp) single nucleotide variant not specified [RCV004247443] Chr1:46274662 [GRCh38]
Chr1:46740334 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.750A>G (p.Glu250=) single nucleotide variant not specified [RCV004247447] Chr1:46260999 [GRCh38]
Chr1:46726671 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1931G>A (p.Cys644Tyr) single nucleotide variant not specified [RCV004247450] Chr1:46277878 [GRCh38]
Chr1:46743550 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2061C>G (p.Ser687Arg) single nucleotide variant not specified [RCV004281408] Chr1:46278099 [GRCh38]
Chr1:46743771 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.521C>A (p.Pro174His) single nucleotide variant not specified [RCV004256348] Chr1:46260770 [GRCh38]
Chr1:46726442 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1410G>C (p.Glu470Asp) single nucleotide variant not specified [RCV004258322] Chr1:46273389 [GRCh38]
Chr1:46739061 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1760G>A (p.Arg587Gln) single nucleotide variant not specified [RCV004260899] Chr1:46274608 [GRCh38]
Chr1:46740280 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.639G>T (p.Lys213Asn) single nucleotide variant not specified [RCV004262806] Chr1:46260888 [GRCh38]
Chr1:46726560 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1901G>A (p.Arg634His) single nucleotide variant not specified [RCV004258308] Chr1:46277848 [GRCh38]
Chr1:46743520 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1768A>T (p.Met590Leu) single nucleotide variant not specified [RCV004326076] Chr1:46274616 [GRCh38]
Chr1:46740288 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.717A>G (p.Gln239=) single nucleotide variant not specified [RCV004326077] Chr1:46260966 [GRCh38]
Chr1:46726638 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1302A>C (p.Ala434=) single nucleotide variant not specified [RCV004326078] Chr1:46272729 [GRCh38]
Chr1:46738401 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1892T>A (p.Ile631Asn) single nucleotide variant not specified [RCV004326079] Chr1:46277839 [GRCh38]
Chr1:46743511 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.458T>C (p.Leu153Ser) single nucleotide variant not specified [RCV004326081] Chr1:46260592 [GRCh38]
Chr1:46726264 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1963C>T (p.His655Tyr) single nucleotide variant not specified [RCV004326082] Chr1:46277910 [GRCh38]
Chr1:46743582 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1678A>T (p.Asn560Tyr) single nucleotide variant not specified [RCV004326083] Chr1:46274205 [GRCh38]
Chr1:46739877 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.64G>A (p.Asp22Asn) single nucleotide variant not specified [RCV004326084] Chr1:46248572 [GRCh38]
Chr1:46714244 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1957G>A (p.Glu653Lys) single nucleotide variant not specified [RCV004326085] Chr1:46277904 [GRCh38]
Chr1:46743576 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2209C>T (p.Gln737Ter) single nucleotide variant Familial cancer of breast [RCV003337945] Chr1:46278247 [GRCh38]
Chr1:46743919 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.15G>A (p.Leu5=) single nucleotide variant not specified [RCV004342406] Chr1:46248523 [GRCh38]
Chr1:46714195 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1158C>A (p.Ser386Arg) single nucleotide variant not specified [RCV004335511] Chr1:46270774 [GRCh38]
Chr1:46736446 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1533T>A (p.Arg511=) single nucleotide variant not specified [RCV004337791] Chr1:46273670 [GRCh38]
Chr1:46739342 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1479G>T (p.Gln493His) single nucleotide variant not specified [RCV004335607] Chr1:46273458 [GRCh38]
Chr1:46739130 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.57C>T (p.Ser19=) single nucleotide variant not specified [RCV004342127] Chr1:46248565 [GRCh38]
Chr1:46714237 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1998C>T (p.Ile666=) single nucleotide variant not specified [RCV004366215] Chr1:46277945 [GRCh38]
Chr1:46743617 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.297C>T (p.Gly99=) single nucleotide variant not specified [RCV004366216] Chr1:46259989 [GRCh38]
Chr1:46725661 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1396A>G (p.Lys466Glu) single nucleotide variant not specified [RCV004366217] Chr1:46273375 [GRCh38]
Chr1:46739047 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2162A>G (p.Gln721Arg) single nucleotide variant not specified [RCV004366218] Chr1:46278200 [GRCh38]
Chr1:46743872 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.254C>T (p.Pro85Leu) single nucleotide variant not specified [RCV004340148] Chr1:46258729 [GRCh38]
Chr1:46724401 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1077G>A (p.Leu359=) single nucleotide variant not specified [RCV004364427] Chr1:46270693 [GRCh38]
Chr1:46736365 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1590G>A (p.Glu530=) single nucleotide variant not specified [RCV004364431] Chr1:46273727 [GRCh38]
Chr1:46739399 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1125G>A (p.Gln375=) single nucleotide variant not specified [RCV004364434] Chr1:46270741 [GRCh38]
Chr1:46736413 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.843T>G (p.His281Gln) single nucleotide variant not specified [RCV004364435] Chr1:46261337 [GRCh38]
Chr1:46727009 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.751A>G (p.Ile251Val) single nucleotide variant not specified [RCV004364428] Chr1:46261000 [GRCh38]
Chr1:46726672 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1353C>T (p.Thr451=) single nucleotide variant not specified [RCV004364437] Chr1:46272780 [GRCh38]
Chr1:46738452 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1658C>T (p.Ala553Val) single nucleotide variant not specified [RCV004366221] Chr1:46274185 [GRCh38]
Chr1:46739857 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1938G>A (p.Val646=) single nucleotide variant not specified [RCV004336034] Chr1:46277885 [GRCh38]
Chr1:46743557 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2010T>C (p.Ala670=) single nucleotide variant not specified [RCV004366219] Chr1:46277957 [GRCh38]
Chr1:46743629 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1896C>A (p.Phe632Leu) single nucleotide variant not specified [RCV004342320] Chr1:46277843 [GRCh38]
Chr1:46743515 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1356G>T (p.Ser452=) single nucleotide variant not specified [RCV004364423] Chr1:46272783 [GRCh38]
Chr1:46738455 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.427G>A (p.Val143Met) single nucleotide variant not specified [RCV004364426] Chr1:46260561 [GRCh38]
Chr1:46726233 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.118G>A (p.Glu40Lys) single nucleotide variant not specified [RCV004364430] Chr1:46250027 [GRCh38]
Chr1:46715699 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1889A>T (p.Lys630Met) single nucleotide variant not specified [RCV004366205] Chr1:46277836 [GRCh38]
Chr1:46743508 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1295A>C (p.Lys432Thr) single nucleotide variant not specified [RCV004366207] Chr1:46272722 [GRCh38]
Chr1:46738394 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1288C>G (p.Gln430Glu) single nucleotide variant not specified [RCV004340250] Chr1:46272715 [GRCh38]
Chr1:46738387 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.251T>G (p.Val84Gly) single nucleotide variant not specified [RCV004364425] Chr1:46258726 [GRCh38]
Chr1:46724398 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.613C>T (p.Pro205Ser) single nucleotide variant not specified [RCV004364429] Chr1:46260862 [GRCh38]
Chr1:46726534 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1380A>C (p.Pro460=) single nucleotide variant not specified [RCV004364432] Chr1:46273359 [GRCh38]
Chr1:46739031 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.619T>A (p.Cys207Ser) single nucleotide variant not specified [RCV004364433] Chr1:46260868 [GRCh38]
Chr1:46726540 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.357T>G (p.Val119=) single nucleotide variant not specified [RCV004364438] Chr1:46260049 [GRCh38]
Chr1:46725721 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2233G>T (p.Gly745Cys) single nucleotide variant not specified [RCV004366206] Chr1:46278271 [GRCh38]
Chr1:46743943 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.7A>T (p.Arg3Trp) single nucleotide variant not specified [RCV004366208] Chr1:46248515 [GRCh38]
Chr1:46714187 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.26A>G (p.Gln9Arg) single nucleotide variant not specified [RCV004366210] Chr1:46248534 [GRCh38]
Chr1:46714206 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.648G>C (p.Val216=) single nucleotide variant not specified [RCV004366211] Chr1:46260897 [GRCh38]
Chr1:46726569 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.538A>C (p.Ile180Leu) single nucleotide variant not specified [RCV004366212] Chr1:46260787 [GRCh38]
Chr1:46726459 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2014C>T (p.Leu672Phe) single nucleotide variant not specified [RCV004366214] Chr1:46277961 [GRCh38]
Chr1:46743633 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1773T>A (p.Phe591Leu) single nucleotide variant not specified [RCV004364424] Chr1:46274621 [GRCh38]
Chr1:46740293 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.564A>G (p.Gly188=) single nucleotide variant not specified [RCV004366209] Chr1:46260813 [GRCh38]
Chr1:46726485 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.95C>A (p.Pro32His) single nucleotide variant not specified [RCV004366213] Chr1:46250004 [GRCh38]
Chr1:46715676 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2142G>A (p.Gly714=) single nucleotide variant not specified [RCV004338124] Chr1:46278180 [GRCh38]
Chr1:46743852 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.30G>A (p.Leu10=) single nucleotide variant not specified [RCV004366220] Chr1:46248538 [GRCh38]
Chr1:46714210 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1424T>C (p.Val475Ala) single nucleotide variant not specified [RCV004359795] Chr1:46273403 [GRCh38]
Chr1:46739075 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.632T>C (p.Ile211Thr) single nucleotide variant not specified [RCV004340418] Chr1:46260881 [GRCh38]
Chr1:46726553 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.959G>T (p.Arg320Leu) single nucleotide variant not specified [RCV004341949] Chr1:46267526 [GRCh38]
Chr1:46733198 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1562A>T (p.Asn521Ile) single nucleotide variant not specified [RCV004358290] Chr1:46273699 [GRCh38]
Chr1:46739371 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.305G>C (p.Arg102Thr) single nucleotide variant not specified [RCV004359776] Chr1:46259997 [GRCh38]
Chr1:46725669 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1782C>G (p.Asp594Glu) single nucleotide variant not specified [RCV004359786] Chr1:46274630 [GRCh38]
Chr1:46740302 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.967A>C (p.Ile323Leu) single nucleotide variant not specified [RCV004359804] Chr1:46267534 [GRCh38]
Chr1:46733206 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.491T>C (p.Leu164Pro) single nucleotide variant not specified [RCV004335871] Chr1:46260740 [GRCh38]
Chr1:46726412 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1542C>T (p.Asp514=) single nucleotide variant not specified [RCV004338164] Chr1:46273679 [GRCh38]
Chr1:46739351 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.227G>A (p.Ser76Asn) single nucleotide variant not specified [RCV004365418] Chr1:46258702 [GRCh38]
Chr1:46724374 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.144G>A (p.Leu48=) single nucleotide variant not specified [RCV004335951] Chr1:46250053 [GRCh38]
Chr1:46715725 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1238G>C (p.Cys413Ser) single nucleotide variant not specified [RCV004365409] Chr1:46272534 [GRCh38]
Chr1:46738206 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.882A>G (p.Ile294Met) single nucleotide variant not specified [RCV004342209] Chr1:46261376 [GRCh38]
Chr1:46727048 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.6G>A (p.Arg2=) single nucleotide variant not specified [RCV004335432] Chr1:46248514 [GRCh38]
Chr1:46714186 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.237A>G (p.Ser79=) single nucleotide variant not specified [RCV004339991] Chr1:46258712 [GRCh38]
Chr1:46724384 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1229A>G (p.Gln410Arg) single nucleotide variant not specified [RCV004335768] Chr1:46272525 [GRCh38]
Chr1:46738197 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.437A>G (p.Asp146Gly) single nucleotide variant Familial cancer of breast [RCV004819030] Chr1:46260571 [GRCh38]
Chr1:46726243 [GRCh37]
uncertain significance
Single allele inversion Bilateral polymicrogyria [RCV003459046] Chr1:33246132..61045156 [GRCh38]
Chr1:1p35.1-31.3
likely pathogenic
NM_003579.4(RAD54L):c.2213G>A (p.Arg738His) single nucleotide variant not provided [RCV003406473] Chr1:46278251 [GRCh38]
Chr1:46743923 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.154C>G (p.Arg52Gly) single nucleotide variant not specified [RCV004445476] Chr1:46250063 [GRCh38]
Chr1:46715735 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.862G>C (p.Gly288Arg) single nucleotide variant not specified [RCV004445480] Chr1:46261356 [GRCh38]
Chr1:46727028 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.866G>A (p.Ser289Asn) single nucleotide variant not specified [RCV004445481] Chr1:46261360 [GRCh38]
Chr1:46727032 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.222T>G (p.Ile74Met) single nucleotide variant not specified [RCV004445477] Chr1:46258697 [GRCh38]
Chr1:46724369 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.737G>T (p.Gly246Val) single nucleotide variant not specified [RCV004445478] Chr1:46260986 [GRCh38]
Chr1:46726658 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1070T>C (p.Phe357Ser) single nucleotide variant not specified [RCV004445475] Chr1:46270686 [GRCh38]
Chr1:46736358 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.785G>A (p.Arg262His) single nucleotide variant not specified [RCV004445479] Chr1:46261279 [GRCh38]
Chr1:46726951 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.343A>G (p.Lys115Glu) single nucleotide variant not specified [RCV004508789] Chr1:46260035 [GRCh38]
Chr1:46725707 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.360G>C (p.Leu120=) single nucleotide variant not specified [RCV004508790] Chr1:46260052 [GRCh38]
Chr1:46725724 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.36G>C (p.Lys12Asn) single nucleotide variant not specified [RCV004508791] Chr1:46248544 [GRCh38]
Chr1:46714216 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.688G>A (p.Val230Ile) single nucleotide variant not specified [RCV004508805] Chr1:46260937 [GRCh38]
Chr1:46726609 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2048G>T (p.Arg683Leu) single nucleotide variant not specified [RCV004508778] Chr1:46278086 [GRCh38]
Chr1:46743758 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2017A>G (p.Ser673Gly) single nucleotide variant not specified [RCV004508777] Chr1:46277964 [GRCh38]
Chr1:46743636 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1974G>C (p.Leu658=) single nucleotide variant not specified [RCV004508776] Chr1:46277921 [GRCh38]
Chr1:46743593 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1027A>G (p.Asn343Asp) single nucleotide variant not specified [RCV004508745] Chr1:46267594 [GRCh38]
Chr1:46733266 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1040T>A (p.Leu347Gln) single nucleotide variant not specified [RCV004508746] Chr1:46267607 [GRCh38]
Chr1:46733279 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1065G>T (p.Lys355Asn) single nucleotide variant not specified [RCV004508747] Chr1:46270681 [GRCh38]
Chr1:46736353 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1156A>G (p.Ser386Gly) single nucleotide variant not specified [RCV004508748] Chr1:46270772 [GRCh38]
Chr1:46736444 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1171T>A (p.Cys391Ser) single nucleotide variant not specified [RCV004508749] Chr1:46272467 [GRCh38]
Chr1:46738139 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.118G>C (p.Glu40Gln) single nucleotide variant not specified [RCV004508750] Chr1:46250027 [GRCh38]
Chr1:46715699 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.11G>T (p.Ser4Ile) single nucleotide variant not specified [RCV004508751] Chr1:46248519 [GRCh38]
Chr1:46714191 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1211T>A (p.Leu404Gln) single nucleotide variant not specified [RCV004508752] Chr1:46272507 [GRCh38]
Chr1:46738179 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1231G>T (p.Val411Phe) single nucleotide variant not specified [RCV004508753] Chr1:46272527 [GRCh38]
Chr1:46738199 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1251A>G (p.Thr417=) single nucleotide variant not specified [RCV004508754] Chr1:46272678 [GRCh38]
Chr1:46738350 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1252C>T (p.Pro418Ser) single nucleotide variant not specified [RCV004508755] Chr1:46272679 [GRCh38]
Chr1:46738351 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1253C>A (p.Pro418His) single nucleotide variant not specified [RCV004508756] Chr1:46272680 [GRCh38]
Chr1:46738352 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1253C>T (p.Pro418Leu) single nucleotide variant not specified [RCV004508757] Chr1:46272680 [GRCh38]
Chr1:46738352 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2168C>T (p.Ala723Val) single nucleotide variant not specified [RCV004508782] Chr1:46278206 [GRCh38]
Chr1:46743878 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2183C>T (p.Ser728Phe) single nucleotide variant not specified [RCV004508783] Chr1:46278221 [GRCh38]
Chr1:46743893 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2203T>G (p.Phe735Val) single nucleotide variant not specified [RCV004508784] Chr1:46278241 [GRCh38]
Chr1:46743913 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2243G>A (p.Ter748=) single nucleotide variant not specified [RCV004508785] Chr1:46278281 [GRCh38]
Chr1:46743953 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.253C>T (p.Pro85Ser) single nucleotide variant not specified [RCV004508786] Chr1:46258728 [GRCh38]
Chr1:46724400 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.27G>T (p.Gln9His) single nucleotide variant not specified [RCV004508787] Chr1:46248535 [GRCh38]
Chr1:46714207 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.292T>C (p.Leu98=) single nucleotide variant not specified [RCV004508788] Chr1:46259984 [GRCh38]
Chr1:46725656 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.389A>C (p.Asp130Ala) single nucleotide variant not specified [RCV004508793] Chr1:46260081 [GRCh38]
Chr1:46725753 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2144T>G (p.Leu715Arg) single nucleotide variant not specified [RCV004508781] Chr1:46278182 [GRCh38]
Chr1:46743854 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.509G>A (p.Ser170Asn) single nucleotide variant not specified [RCV004508801] Chr1:46260758 [GRCh38]
Chr1:46726430 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.541A>C (p.Met181Leu) single nucleotide variant not specified [RCV004508802] Chr1:46260790 [GRCh38]
Chr1:46726462 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.754G>A (p.Asp252Asn) single nucleotide variant not specified [RCV004508809] Chr1:46261003 [GRCh38]
Chr1:46726675 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.768A>G (p.Glu256=) single nucleotide variant not specified [RCV004508811] Chr1:46261262 [GRCh38]
Chr1:46726934 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.776T>A (p.Met259Lys) single nucleotide variant not specified [RCV004508812] Chr1:46261270 [GRCh38]
Chr1:46726942 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.803C>A (p.Ser268Tyr) single nucleotide variant not specified [RCV004508813] Chr1:46261297 [GRCh38]
Chr1:46726969 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.871G>T (p.Gly291Cys) single nucleotide variant not specified [RCV004508815] Chr1:46261365 [GRCh38]
Chr1:46727037 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.8G>A (p.Arg3Lys) single nucleotide variant not specified [RCV004508817] Chr1:46248516 [GRCh38]
Chr1:46714188 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.900G>A (p.Arg300=) single nucleotide variant not specified [RCV004508818] Chr1:46267467 [GRCh38]
Chr1:46733139 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.919C>G (p.Gln307Glu) single nucleotide variant not specified [RCV004508820] Chr1:46267486 [GRCh38]
Chr1:46733158 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.935T>A (p.Leu312Gln) single nucleotide variant not specified [RCV004508821] Chr1:46267502 [GRCh38]
Chr1:46733174 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.98G>A (p.Arg33Lys) single nucleotide variant not specified [RCV004508822] Chr1:46250007 [GRCh38]
Chr1:46715679 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.997C>T (p.Leu333Phe) single nucleotide variant not specified [RCV004508823] Chr1:46267564 [GRCh38]
Chr1:46733236 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2132A>T (p.Asp711Val) single nucleotide variant not specified [RCV004508780] Chr1:46278170 [GRCh38]
Chr1:46743842 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2067G>C (p.Gln689His) single nucleotide variant not specified [RCV004508779] Chr1:46278105 [GRCh38]
Chr1:46743777 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1921C>T (p.Leu641=) single nucleotide variant not specified [RCV004508774] Chr1:46277868 [GRCh38]
Chr1:46743540 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1847G>A (p.Cys616Tyr) single nucleotide variant not specified [RCV004508773] Chr1:46274695 [GRCh38]
Chr1:46740367 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1780G>T (p.Asp594Tyr) single nucleotide variant not specified [RCV004508772] Chr1:46274628 [GRCh38]
Chr1:46740300 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1722A>G (p.Lys574=) single nucleotide variant not specified [RCV004508771] Chr1:46274570 [GRCh38]
Chr1:46740242 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1709T>G (p.Met570Arg) single nucleotide variant not specified [RCV004508770] Chr1:46274557 [GRCh38]
Chr1:46740229 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1680T>C (p.Asn560=) single nucleotide variant not specified [RCV004508769] Chr1:46274207 [GRCh38]
Chr1:46739879 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1522A>G (p.Thr508Ala) single nucleotide variant not specified [RCV004508768] Chr1:46273659 [GRCh38]
Chr1:46739331 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1496T>G (p.Leu499Arg) single nucleotide variant not specified [RCV004508767] Chr1:46273633 [GRCh38]
Chr1:46739305 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1437C>G (p.Asp479Glu) single nucleotide variant not specified [RCV004508766] Chr1:46273416 [GRCh38]
Chr1:46739088 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1422T>C (p.Phe474=) single nucleotide variant not specified [RCV004508765] Chr1:46273401 [GRCh38]
Chr1:46739073 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1397A>T (p.Lys466Met) single nucleotide variant not specified [RCV004508762] Chr1:46273376 [GRCh38]
Chr1:46739048 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1392T>C (p.Tyr464=) single nucleotide variant not specified [RCV004508761] Chr1:46273371 [GRCh38]
Chr1:46739043 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1345T>C (p.Ser449Pro) single nucleotide variant not specified [RCV004508760] Chr1:46272772 [GRCh38]
Chr1:46738444 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1328G>A (p.Ser443Asn) single nucleotide variant not specified [RCV004508759] Chr1:46272755 [GRCh38]
Chr1:46738427 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1323G>A (p.Lys441=) single nucleotide variant not specified [RCV004508758] Chr1:46272750 [GRCh38]
Chr1:46738422 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.425A>T (p.His142Leu) single nucleotide variant not specified [RCV004508794] Chr1:46260559 [GRCh38]
Chr1:46726231 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.436G>T (p.Asp146Tyr) single nucleotide variant not specified [RCV004508795] Chr1:46260570 [GRCh38]
Chr1:46726242 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.438C>A (p.Asp146Glu) single nucleotide variant not specified [RCV004508796] Chr1:46260572 [GRCh38]
Chr1:46726244 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.44C>T (p.Pro15Leu) single nucleotide variant not specified [RCV004508797] Chr1:46248552 [GRCh38]
Chr1:46714224 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.464C>T (p.Pro155Leu) single nucleotide variant not specified [RCV004508798] Chr1:46260598 [GRCh38]
Chr1:46726270 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.502G>A (p.Val168Ile) single nucleotide variant not specified [RCV004508799] Chr1:46260751 [GRCh38]
Chr1:46726423 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.508A>G (p.Ser170Gly) single nucleotide variant not specified [RCV004508800] Chr1:46260757 [GRCh38]
Chr1:46726429 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.542T>C (p.Met181Thr) single nucleotide variant not specified [RCV004508803] Chr1:46260791 [GRCh38]
Chr1:46726463 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.646G>A (p.Val216Met) single nucleotide variant not specified [RCV004508804] Chr1:46260895 [GRCh38]
Chr1:46726567 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.696A>G (p.Lys232=) single nucleotide variant not specified [RCV004508806] Chr1:46260945 [GRCh38]
Chr1:46726617 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.724G>A (p.Ala242Thr) single nucleotide variant not specified [RCV004508807] Chr1:46260973 [GRCh38]
Chr1:46726645 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.725C>T (p.Ala242Val) single nucleotide variant not specified [RCV004508808] Chr1:46260974 [GRCh38]
Chr1:46726646 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.756C>A (p.Asp252Glu) single nucleotide variant not specified [RCV004508810] Chr1:46261005 [GRCh38]
Chr1:46726677 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.830C>T (p.Thr277Ile) single nucleotide variant not specified [RCV004508814] Chr1:46261324 [GRCh38]
Chr1:46726996 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.872G>A (p.Gly291Asp) single nucleotide variant not specified [RCV004508816] Chr1:46261366 [GRCh38]
Chr1:46727038 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1405G>A (p.Glu469Lys) single nucleotide variant not specified [RCV004508764] Chr1:46273384 [GRCh38]
Chr1:46739056 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1399T>C (p.Cys467Arg) single nucleotide variant not specified [RCV004508763] Chr1:46273378 [GRCh38]
Chr1:46739050 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.829A>C (p.Thr277Pro) single nucleotide variant not specified [RCV004665265] Chr1:46261323 [GRCh38]
Chr1:46726995 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1917G>T (p.Lys639Asn) single nucleotide variant not specified [RCV004669493] Chr1:46277864 [GRCh38]
Chr1:46743536 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.353T>C (p.Leu118Ser) single nucleotide variant not specified [RCV004665222] Chr1:46260045 [GRCh38]
Chr1:46725717 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2005G>A (p.Glu669Lys) single nucleotide variant not specified [RCV004665282] Chr1:46277952 [GRCh38]
Chr1:46743624 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1071T>G (p.Phe357Leu) single nucleotide variant not specified [RCV004669489] Chr1:46270687 [GRCh38]
Chr1:46736359 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.815T>C (p.Ile272Thr) single nucleotide variant not specified [RCV004665239] Chr1:46261309 [GRCh38]
Chr1:46726981 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.814A>C (p.Ile272Leu) single nucleotide variant not specified [RCV004665240] Chr1:46261308 [GRCh38]
Chr1:46726980 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.678G>T (p.Trp226Cys) single nucleotide variant not specified [RCV004665243] Chr1:46260927 [GRCh38]
Chr1:46726599 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.733G>A (p.Gly245Arg) single nucleotide variant not specified [RCV004665246] Chr1:46260982 [GRCh38]
Chr1:46726654 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.988A>G (p.Asn330Asp) single nucleotide variant not specified [RCV004665249] Chr1:46267555 [GRCh38]
Chr1:46733227 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.371C>T (p.Pro124Leu) single nucleotide variant not specified [RCV004665253] Chr1:46260063 [GRCh38]
Chr1:46725735 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1665T>C (p.Val555=) single nucleotide variant not specified [RCV004665264] Chr1:46274192 [GRCh38]
Chr1:46739864 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1123C>A (p.Gln375Lys) single nucleotide variant not specified [RCV004665274] Chr1:46270739 [GRCh38]
Chr1:46736411 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2141G>A (p.Gly714Glu) single nucleotide variant not specified [RCV004665225] Chr1:46278179 [GRCh38]
Chr1:46743851 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.209A>G (p.His70Arg) single nucleotide variant not specified [RCV004665220] Chr1:46250118 [GRCh38]
Chr1:46715790 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1470G>A (p.Leu490=) single nucleotide variant not specified [RCV004665221] Chr1:46273449 [GRCh38]
Chr1:46739121 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.694A>G (p.Lys232Glu) single nucleotide variant not specified [RCV004665224] Chr1:46260943 [GRCh38]
Chr1:46726615 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1319G>A (p.Gly440Asp) single nucleotide variant not specified [RCV004665236] Chr1:46272746 [GRCh38]
Chr1:46738418 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1364A>C (p.Lys455Thr) single nucleotide variant not specified [RCV004665237] Chr1:46272791 [GRCh38]
Chr1:46738463 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.470A>G (p.Gln157Arg) single nucleotide variant not specified [RCV004665244] Chr1:46260604 [GRCh38]
Chr1:46726276 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1596G>C (p.Leu532=) single nucleotide variant not specified [RCV004665245] Chr1:46273733 [GRCh38]
Chr1:46739405 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1434G>C (p.Leu478Phe) single nucleotide variant not specified [RCV004665248] Chr1:46273413 [GRCh38]
Chr1:46739085 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1423G>T (p.Val475Leu) single nucleotide variant not specified [RCV004665257] Chr1:46273402 [GRCh38]
Chr1:46739074 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1464G>C (p.Lys488Asn) single nucleotide variant not specified [RCV004665263] Chr1:46273443 [GRCh38]
Chr1:46739115 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.392A>C (p.Gln131Pro) single nucleotide variant not specified [RCV004665269] Chr1:46260084 [GRCh38]
Chr1:46725756 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1274A>T (p.Lys425Met) single nucleotide variant not specified [RCV004665233] Chr1:46272701 [GRCh38]
Chr1:46738373 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.625C>G (p.Pro209Ala) single nucleotide variant not specified [RCV004665278] Chr1:46260874 [GRCh38]
Chr1:46726546 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1907G>A (p.Ser636Asn) single nucleotide variant not specified [RCV004665285] Chr1:46277854 [GRCh38]
Chr1:46743526 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.311G>T (p.Gly104Val) single nucleotide variant not specified [RCV004669491] Chr1:46260003 [GRCh38]
Chr1:46725675 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1896C>T (p.Phe632=) single nucleotide variant not specified [RCV004669499] Chr1:46277843 [GRCh38]
Chr1:46743515 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2192T>C (p.Ile731Thr) single nucleotide variant not specified [RCV004665270] Chr1:46278230 [GRCh38]
Chr1:46743902 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1891A>C (p.Ile631Leu) single nucleotide variant not specified [RCV004665256] Chr1:46277838 [GRCh38]
Chr1:46743510 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2040C>G (p.His680Gln) single nucleotide variant not specified [RCV004665255] Chr1:46278078 [GRCh38]
Chr1:46743750 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2152G>A (p.Glu718Lys) single nucleotide variant not specified [RCV004665277] Chr1:46278190 [GRCh38]
Chr1:46743862 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1925G>A (p.Ser642Asn) single nucleotide variant not specified [RCV004665254] Chr1:46277872 [GRCh38]
Chr1:46743544 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2070C>T (p.Ile690=) single nucleotide variant not specified [RCV004665228] Chr1:46278108 [GRCh38]
Chr1:46743780 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1657G>C (p.Ala553Pro) single nucleotide variant not specified [RCV004665223] Chr1:46274184 [GRCh38]
Chr1:46739856 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.733G>C (p.Gly245Arg) single nucleotide variant not specified [RCV004665230] Chr1:46260982 [GRCh38]
Chr1:46726654 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1357C>T (p.Leu453=) single nucleotide variant not specified [RCV004665231] Chr1:46272784 [GRCh38]
Chr1:46738456 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1692C>G (p.Ser564Arg) single nucleotide variant not specified [RCV004665247] Chr1:46274540 [GRCh38]
Chr1:46740212 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.712A>G (p.Ile238Val) single nucleotide variant not specified [RCV004665252] Chr1:46260961 [GRCh38]
Chr1:46726633 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.453G>C (p.Lys151Asn) single nucleotide variant not specified [RCV004665258] Chr1:46260587 [GRCh38]
Chr1:46726259 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.139T>G (p.Phe47Val) single nucleotide variant not specified [RCV004665262] Chr1:46250048 [GRCh38]
Chr1:46715720 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.335C>G (p.Pro112Arg) single nucleotide variant not specified [RCV004665279] Chr1:46260027 [GRCh38]
Chr1:46725699 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.143T>G (p.Leu48Arg) single nucleotide variant not specified [RCV004665272] Chr1:46250052 [GRCh38]
Chr1:46715724 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2084A>C (p.Asp695Ala) single nucleotide variant not specified [RCV004665273] Chr1:46278122 [GRCh38]
Chr1:46743794 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.718C>G (p.Pro240Ala) single nucleotide variant not specified [RCV004665259] Chr1:46260967 [GRCh38]
Chr1:46726639 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1435G>A (p.Asp479Asn) single nucleotide variant not specified [RCV004665271] Chr1:46273414 [GRCh38]
Chr1:46739086 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.874C>G (p.Leu292Val) single nucleotide variant not specified [RCV004665281] Chr1:46261368 [GRCh38]
Chr1:46727040 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.2049T>C (p.Arg683=) single nucleotide variant not specified [RCV004669487] Chr1:46278087 [GRCh38]
Chr1:46743759 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1953T>C (p.Asp651=) single nucleotide variant not specified [RCV004665268] Chr1:46277900 [GRCh38]
Chr1:46743572 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2143C>A (p.Leu715Ile) single nucleotide variant not specified [RCV004665227] Chr1:46278181 [GRCh38]
Chr1:46743853 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.255C>T (p.Pro85=) single nucleotide variant not specified [RCV004669486] Chr1:46258730 [GRCh38]
Chr1:46724402 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.825T>C (p.Tyr275=) single nucleotide variant not specified [RCV004669488] Chr1:46261319 [GRCh38]
Chr1:46726991 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1013T>C (p.Leu338Ser) single nucleotide variant not specified [RCV004665234] Chr1:46267580 [GRCh38]
Chr1:46733252 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.20C>T (p.Pro7Leu) single nucleotide variant not specified [RCV004665238] Chr1:46248528 [GRCh38]
Chr1:46714200 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.979C>A (p.Pro327Thr) single nucleotide variant not specified [RCV004665250] Chr1:46267546 [GRCh38]
Chr1:46733218 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.146C>A (p.Ser49Tyr) single nucleotide variant not specified [RCV004665251] Chr1:46250055 [GRCh38]
Chr1:46715727 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1579G>T (p.Asp527Tyr) single nucleotide variant not specified [RCV004665261] Chr1:46273716 [GRCh38]
Chr1:46739388 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.228C>G (p.Ser76Arg) single nucleotide variant not specified [RCV004665266] Chr1:46258703 [GRCh38]
Chr1:46724375 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1282C>G (p.Leu428Val) single nucleotide variant not specified [RCV004665275] Chr1:46272709 [GRCh38]
Chr1:46738381 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1154C>A (p.Thr385Asn) single nucleotide variant not specified [RCV004665280] Chr1:46270770 [GRCh38]
Chr1:46736442 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.547G>C (p.Asp183His) single nucleotide variant not specified [RCV004665284] Chr1:46260796 [GRCh38]
Chr1:46726468 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1123C>G (p.Gln375Glu) single nucleotide variant not specified [RCV004665286] Chr1:46270739 [GRCh38]
Chr1:46736411 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1899G>C (p.Gln633His) single nucleotide variant not specified [RCV004669494] Chr1:46277846 [GRCh38]
Chr1:46743518 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.1986G>A (p.Lys662=) single nucleotide variant not specified [RCV004665232] Chr1:46277933 [GRCh38]
Chr1:46743605 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.2145C>G (p.Leu715=) single nucleotide variant not specified [RCV004669501] Chr1:46278183 [GRCh38]
Chr1:46743855 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1143G>T (p.Leu381=) single nucleotide variant not specified [RCV004669492] Chr1:46270759 [GRCh38]
Chr1:46736431 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.187C>G (p.Pro63Ala) single nucleotide variant not specified [RCV004669495] Chr1:46250096 [GRCh38]
Chr1:46715768 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.969C>A (p.Ile323=) single nucleotide variant not specified [RCV004669496] Chr1:46267536 [GRCh38]
Chr1:46733208 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1462A>G (p.Lys488Glu) single nucleotide variant not specified [RCV004669497] Chr1:46273441 [GRCh38]
Chr1:46739113 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.924T>C (p.Thr308=) single nucleotide variant not specified [RCV004669498] Chr1:46267491 [GRCh38]
Chr1:46733163 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1779T>G (p.Pro593=) single nucleotide variant not specified [RCV004669500] Chr1:46274627 [GRCh38]
Chr1:46740299 [GRCh37]
Chr1:1p34.1
likely benign
NM_003579.4(RAD54L):c.1770G>C (p.Met590Ile) single nucleotide variant not specified [RCV004669502] Chr1:46274618 [GRCh38]
Chr1:46740290 [GRCh37]
Chr1:1p34.1
uncertain significance
NM_003579.4(RAD54L):c.267T>G (p.Tyr89Ter) single nucleotide variant Lymphoma, non-Hodgkin, familial [RCV004764674] Chr1:46258742 [GRCh38]
Chr1:46724414 [GRCh37]
Chr1:1p34.1
likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2693
Count of miRNA genes:884
Interacting mature miRNAs:1073
Transcripts:ENST00000371975, ENST00000442598, ENST00000459678, ENST00000463715, ENST00000469835, ENST00000472889, ENST00000473251, ENST00000476687, ENST00000487700, ENST00000488942, ENST00000493032, ENST00000493985
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
2314561GLUCO47_HGlucose level QTL 47 (human)1.1Glucose level14477336070773360Human

Markers in Region
RH93140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37146,743,180 - 46,743,336UniSTSGRCh37
Build 36146,515,767 - 46,515,923RGDNCBI36
Celera145,030,560 - 45,030,716RGD
Cytogenetic Map1p32UniSTS
HuRef144,859,023 - 44,859,179UniSTS
GeneMap99-GB4 RH Map1143.98UniSTS
RH47045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37146,743,954 - 46,744,084UniSTSGRCh37
Build 36146,516,541 - 46,516,671RGDNCBI36
Celera145,031,334 - 45,031,464RGD
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map1p32UniSTS
HuRef144,859,797 - 44,859,927UniSTS
GeneMap99-GB4 RH Map1144.4UniSTS
RAD54L_8807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37146,743,794 - 46,744,289UniSTSGRCh37
Build 36146,516,381 - 46,516,876RGDNCBI36
Celera145,031,174 - 45,031,669RGD
HuRef144,859,637 - 44,860,132UniSTS
SHGC-74777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37146,743,860 - 46,743,969UniSTSGRCh37
Build 36146,516,447 - 46,516,556RGDNCBI36
Celera145,031,240 - 45,031,349RGD
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map1p32UniSTS
HuRef144,859,703 - 44,859,812UniSTS
TNG Radiation Hybrid Map123751.0UniSTS
GeneMap99-GB4 RH Map1144.4UniSTS
RH70932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37146,744,161 - 46,744,370UniSTSGRCh37
Build 36146,516,748 - 46,516,957RGDNCBI36
Celera145,031,541 - 45,031,750RGD
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map1p32UniSTS
HuRef144,860,004 - 44,860,213UniSTS
GeneMap99-GB4 RH Map1143.72UniSTS
NCBI RH Map1294.0UniSTS
RH70950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37146,743,944 - 46,744,079UniSTSGRCh37
Build 36146,516,531 - 46,516,666RGDNCBI36
Celera145,031,324 - 45,031,459RGD
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map1p32UniSTS
HuRef144,859,787 - 44,859,922UniSTS
GeneMap99-GB4 RH Map1144.91UniSTS
NCBI RH Map1294.0UniSTS
MARC_7379-7380:996687836:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37146,724,386 - 46,725,736UniSTSGRCh37
Celera145,011,765 - 45,013,115UniSTS
HuRef144,840,149 - 44,841,499UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1202 2432 2780 2232 4944 1712 2338 5 611 1938 453 2267 7252 6429 52 3708 849 1735 1615 172

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370766 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011542299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011542300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA582917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL121602 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY623117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC121059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC121060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM464345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM678712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB048280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB449264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X97795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000371975   ⟹   ENSP00000361043
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,763 - 46,278,473 (+)Ensembl
Ensembl Acc Id: ENST00000442598   ⟹   ENSP00000396113
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,695 - 46,278,473 (+)Ensembl
Ensembl Acc Id: ENST00000459678   ⟹   ENSP00000479155
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,272,505 - 46,278,145 (+)Ensembl
Ensembl Acc Id: ENST00000463715   ⟹   ENSP00000480207
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,688 - 46,261,358 (+)Ensembl
Ensembl Acc Id: ENST00000469835   ⟹   ENSP00000477172
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,769 - 46,260,879 (+)Ensembl
Ensembl Acc Id: ENST00000472889   ⟹   ENSP00000477729
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,259,964 - 46,267,608 (+)Ensembl
Ensembl Acc Id: ENST00000473251   ⟹   ENSP00000483843
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,260,848 - 46,272,800 (+)Ensembl
Ensembl Acc Id: ENST00000476687   ⟹   ENSP00000479734
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,261,338 - 46,273,681 (+)Ensembl
Ensembl Acc Id: ENST00000487700
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,248,512 - 46,267,584 (+)Ensembl
Ensembl Acc Id: ENST00000488942   ⟹   ENSP00000476642
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,272,466 - 46,278,439 (+)Ensembl
Ensembl Acc Id: ENST00000493032   ⟹   ENSP00000479995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,248,512 - 46,261,015 (+)Ensembl
Ensembl Acc Id: ENST00000493985   ⟹   ENSP00000479823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,700 - 46,261,015 (+)Ensembl
Ensembl Acc Id: ENST00000655446   ⟹   ENSP00000499451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,797 - 46,278,467 (+)Ensembl
Ensembl Acc Id: ENST00000657122   ⟹   ENSP00000499519
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,248,238 - 46,260,568 (+)Ensembl
Ensembl Acc Id: ENST00000661174
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,246,461 - 46,248,584 (+)Ensembl
Ensembl Acc Id: ENST00000661701   ⟹   ENSP00000499340
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,270,659 - 46,278,472 (+)Ensembl
Ensembl Acc Id: ENST00000664182
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,267,505 - 46,273,670 (+)Ensembl
Ensembl Acc Id: ENST00000668390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,069 - 46,250,008 (+)Ensembl
Ensembl Acc Id: ENST00000668565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,258,707 - 46,260,161 (+)Ensembl
Ensembl Acc Id: ENST00000669994   ⟹   ENSP00000499311
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,715 - 46,260,928 (+)Ensembl
Ensembl Acc Id: ENST00000671528   ⟹   ENSP00000499652
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl146,247,700 - 46,278,480 (+)Ensembl
RefSeq Acc Id: NM_001142548   ⟹   NP_001136020
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38146,247,688 - 46,278,473 (+)NCBI
GRCh37146,713,367 - 46,744,145 (+)NCBI
HuRef144,829,132 - 44,859,988 (+)ENTREZGENE
CHM1_1146,830,372 - 46,861,163 (+)NCBI
T2T-CHM13v2.0146,124,906 - 46,155,694 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001370766   ⟹   NP_001357695
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38146,247,688 - 46,278,473 (+)NCBI
T2T-CHM13v2.0146,124,906 - 46,155,694 (+)NCBI
Sequence:
RefSeq Acc Id: NM_003579   ⟹   NP_003570
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38146,247,763 - 46,278,473 (+)NCBI
GRCh37146,713,367 - 46,744,145 (+)ENTREZGENE
GRCh37146,713,367 - 46,744,145 (+)NCBI
Build 36146,486,004 - 46,516,732 (+)NCBI Archive
HuRef144,829,132 - 44,859,988 (+)ENTREZGENE
CHM1_1146,830,372 - 46,861,163 (+)NCBI
T2T-CHM13v2.0146,124,981 - 46,155,694 (+)NCBI
Sequence:
RefSeq Acc Id: NP_003570   ⟸   NM_003579
- Peptide Label: isoform 1
- UniProtKB: Q5TE31 (UniProtKB/Swiss-Prot),   Q6IUY3 (UniProtKB/Swiss-Prot),   Q92698 (UniProtKB/Swiss-Prot),   A8K996 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136020   ⟸   NM_001142548
- Peptide Label: isoform 1
- UniProtKB: Q5TE31 (UniProtKB/Swiss-Prot),   Q6IUY3 (UniProtKB/Swiss-Prot),   Q92698 (UniProtKB/Swiss-Prot),   A8K996 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001357695   ⟸   NM_001370766
- Peptide Label: isoform 2
- UniProtKB: B4DLX7 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000480207   ⟸   ENST00000463715
Ensembl Acc Id: ENSP00000361043   ⟸   ENST00000371975
Ensembl Acc Id: ENSP00000499340   ⟸   ENST00000661701
Ensembl Acc Id: ENSP00000479995   ⟸   ENST00000493032
Ensembl Acc Id: ENSP00000479823   ⟸   ENST00000493985
Ensembl Acc Id: ENSP00000477172   ⟸   ENST00000469835
Ensembl Acc Id: ENSP00000396113   ⟸   ENST00000442598
Ensembl Acc Id: ENSP00000499311   ⟸   ENST00000669994
Ensembl Acc Id: ENSP00000499451   ⟸   ENST00000655446
Ensembl Acc Id: ENSP00000479155   ⟸   ENST00000459678
Ensembl Acc Id: ENSP00000499519   ⟸   ENST00000657122
Ensembl Acc Id: ENSP00000477729   ⟸   ENST00000472889
Ensembl Acc Id: ENSP00000483843   ⟸   ENST00000473251
Ensembl Acc Id: ENSP00000476642   ⟸   ENST00000488942
Ensembl Acc Id: ENSP00000499652   ⟸   ENST00000671528
Ensembl Acc Id: ENSP00000479734   ⟸   ENST00000476687
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q92698-F1-model_v2 AlphaFold Q92698 1-747 view protein structure

Promoters
RGD ID:6855402
Promoter ID:EPDNEW_H866
Type:initiation region
Name:RAD54L_1
Description:RAD54 like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38146,247,763 - 46,247,823EPDNEW
RGD ID:6786382
Promoter ID:HG_KWN:2550
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001142548,   NM_003579,   OTTHUMT00000021273,   OTTHUMT00000021274,   OTTHUMT00000021276,   OTTHUMT00000021277,   OTTHUMT00000021278
Position:
Human AssemblyChrPosition (strand)Source
Build 36146,485,131 - 46,486,507 (+)MPROMDB
RGD ID:6786383
Promoter ID:HG_KWN:2554
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000021281,   OTTHUMT00000021282
Position:
Human AssemblyChrPosition (strand)Source
Build 36146,510,809 - 46,511,309 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9826 AgrOrtholog
COSMIC RAD54L COSMIC
Ensembl Genes ENSG00000085999 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000371975 ENTREZGENE
  ENST00000371975.9 UniProtKB/Swiss-Prot
  ENST00000442598 ENTREZGENE
  ENST00000442598.5 UniProtKB/Swiss-Prot
  ENST00000459678.2 UniProtKB/TrEMBL
  ENST00000463715.5 UniProtKB/TrEMBL
  ENST00000469835.6 UniProtKB/TrEMBL
  ENST00000472889.2 UniProtKB/TrEMBL
  ENST00000473251.2 UniProtKB/TrEMBL
  ENST00000476687.2 UniProtKB/TrEMBL
  ENST00000488942.5 UniProtKB/TrEMBL
  ENST00000493032.5 UniProtKB/TrEMBL
  ENST00000493985.5 UniProtKB/TrEMBL
  ENST00000655446.1 UniProtKB/TrEMBL
  ENST00000657122.1 UniProtKB/TrEMBL
  ENST00000661701.1 UniProtKB/TrEMBL
  ENST00000669994.1 UniProtKB/TrEMBL
  ENST00000671528.1 UniProtKB/Swiss-Prot
Gene3D-CATH 3.40.50.10810 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SWI2/SNF2 ATPases, N-terminal domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000085999 GTEx
HGNC ID HGNC:9826 ENTREZGENE
Human Proteome Map RAD54L Human Proteome Map
InterPro Helicase_ATP-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Helicase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2/RAD54-like_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2_RAD54_helicase_repair UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8438 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8438 ENTREZGENE
OMIM 603615 OMIM
PANTHER DNA EXCISION REPAIR PROTEIN ERCC-6-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2/RAD54 FAMILY MEMBER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Helicase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SNF2_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34181 PharmGKB
PROSITE HELICASE_ATP_BIND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HELICASE_CTER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DEXDc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HELICc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WTB0_HUMAN UniProtKB/TrEMBL
  A0A087WV39_HUMAN UniProtKB/TrEMBL
  A0A087WVW5_HUMAN UniProtKB/TrEMBL
  A0A087WW72_HUMAN UniProtKB/TrEMBL
  A0A087WWG5_HUMAN UniProtKB/TrEMBL
  A0A087X124_HUMAN UniProtKB/TrEMBL
  A0A590UJ71_HUMAN UniProtKB/TrEMBL
  A0A590UJ90_HUMAN UniProtKB/TrEMBL
  A0A590UJJ7_HUMAN UniProtKB/TrEMBL
  A0A590UJQ8_HUMAN UniProtKB/TrEMBL
  A8K996 ENTREZGENE, UniProtKB/TrEMBL
  B4DLX7 ENTREZGENE, UniProtKB/TrEMBL
  L8E913_HUMAN UniProtKB/TrEMBL
  Q5TE31 ENTREZGENE
  Q6IUY3 ENTREZGENE
  Q92698 ENTREZGENE, UniProtKB/Swiss-Prot
  V9GYD3_HUMAN UniProtKB/TrEMBL
  V9GYX6_HUMAN UniProtKB/TrEMBL
UniProt Secondary Q5TE31 UniProtKB/Swiss-Prot
  Q6IUY3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-08-15 RAD54L  RAD54 like  RAD54L  RAD54 like (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED
2017-02-28 RAD54L  RAD54 like (S. cerevisiae)  RAD54L  RAD54-like (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED