FBXO7 (F-box protein 7) - Rat Genome Database

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Gene: FBXO7 (F-box protein 7) Homo sapiens
Analyze
Symbol: FBXO7
Name: F-box protein 7
RGD ID: 1313800
HGNC Page HGNC:13586
Description: Enables several functions, including enzyme binding activity; protein heterodimerization activity; and ubiquitin-like ligase-substrate adaptor activity. Involved in several processes, including positive regulation of mitophagy; protein K48-linked ubiquitination; and protein targeting to mitochondrion. Located in several cellular components, including Lewy body core; Lewy body corona; and Lewy neurite. Part of SCF ubiquitin ligase complex. Is active in nucleus. Implicated in Parkinson's disease and Parkinson's disease 15.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp686B08113; F-box only protein 7; FBX; FBX07; FBX7; PARK15; PKPS
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
GRCh382232,474,811 - 32,498,829 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2232,474,676 - 32,498,829 (+)EnsemblGRCh38hg38GRCh38
GRCh372232,870,798 - 32,894,816 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362231,200,707 - 31,224,818 (+)NCBINCBI36Build 36hg18NCBI36
Build 342231,195,263 - 31,219,369NCBI
Celera2216,672,879 - 16,696,990 (+)NCBICelera
Cytogenetic Map22q12.3NCBI
HuRef2215,827,931 - 15,852,000 (+)NCBIHuRef
CHM1_12232,830,063 - 32,854,178 (+)NCBICHM1_1
T2T-CHM13v2.02232,938,705 - 32,962,724 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

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

References - curated
# Reference Title Reference Citation
1. Genes associated with Parkinson's disease: regulation of autophagy and beyond. Beilina A and Cookson MR, J Neurochem. 2015 Jul 30. doi: 10.1111/jnc.13266.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
6. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
Additional References at PubMed
PMID:10531035   PMID:10531037   PMID:10591208   PMID:10737800   PMID:10945468   PMID:11076863   PMID:11256614   PMID:12477932   PMID:12527899   PMID:12529303   PMID:14702039   PMID:15145941  
PMID:15461802   PMID:15489334   PMID:15489336   PMID:16196087   PMID:16278047   PMID:16381901   PMID:16510124   PMID:16581786   PMID:18495667   PMID:18624398   PMID:19028597   PMID:19038853  
PMID:19615732   PMID:19820697   PMID:20301402   PMID:20603184   PMID:20669327   PMID:21139048   PMID:21145461   PMID:21347293   PMID:21378169   PMID:21653829   PMID:21695055   PMID:21873635  
PMID:21890473   PMID:21906983   PMID:21963094   PMID:21988832   PMID:22212761   PMID:22490479   PMID:22505724   PMID:22632967   PMID:23133663   PMID:23196729   PMID:23222517   PMID:23318512  
PMID:23352116   PMID:23656991   PMID:23933751   PMID:24112787   PMID:24419388   PMID:24811749   PMID:24947323   PMID:25029497   PMID:25085748   PMID:25169713   PMID:25416956   PMID:25910212  
PMID:26010069   PMID:26186194   PMID:26245297   PMID:26310625   PMID:26496610   PMID:26882974   PMID:26965690   PMID:27497298   PMID:27503909   PMID:27565346   PMID:27689878   PMID:27705803  
PMID:28514442   PMID:28581483   PMID:29103612   PMID:29117863   PMID:29134665   PMID:29370161   PMID:29987050   PMID:30026574   PMID:30232368   PMID:30454685   PMID:30463901   PMID:30759391  
PMID:31515488   PMID:32274857   PMID:32423001   PMID:32493843   PMID:32628020   PMID:32814053   PMID:32877691   PMID:32933748   PMID:33002721   PMID:33010352   PMID:33291077   PMID:33504946  
PMID:33774278   PMID:33961781   PMID:34060591   PMID:34791250   PMID:34800438   PMID:35211260   PMID:35242855   PMID:35509820   PMID:35670764   PMID:35831314   PMID:35914814   PMID:35944360  
PMID:36215168   PMID:36261086   PMID:36274328   PMID:36646384   PMID:37028429   PMID:37071682   PMID:37317656   PMID:37344480   PMID:37822160   PMID:37827155   PMID:37874827   PMID:38839752  


Genomics

Comparative Map Data
FBXO7
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382232,474,811 - 32,498,829 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2232,474,676 - 32,498,829 (+)EnsemblGRCh38hg38GRCh38
GRCh372232,870,798 - 32,894,816 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362231,200,707 - 31,224,818 (+)NCBINCBI36Build 36hg18NCBI36
Build 342231,195,263 - 31,219,369NCBI
Celera2216,672,879 - 16,696,990 (+)NCBICelera
Cytogenetic Map22q12.3NCBI
HuRef2215,827,931 - 15,852,000 (+)NCBIHuRef
CHM1_12232,830,063 - 32,854,178 (+)NCBICHM1_1
T2T-CHM13v2.02232,938,705 - 32,962,724 (+)NCBIT2T-CHM13v2.0
Fbxo7
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391085,856,313 - 85,887,737 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1085,857,836 - 85,887,737 (+)EnsemblGRCm39 Ensembl
GRCm381086,020,449 - 86,051,873 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1086,021,972 - 86,051,873 (+)EnsemblGRCm38mm10GRCm38
MGSCv371085,484,674 - 85,511,073 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361085,451,796 - 85,478,128 (+)NCBIMGSCv36mm8
Celera1087,995,701 - 88,022,106 (+)NCBICelera
Cytogenetic Map10C1NCBI
cM Map1041.91NCBI
Fbxo7
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8719,696,951 - 19,725,180 (-)NCBIGRCr8
mRatBN7.2717,809,224 - 17,837,549 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl717,809,231 - 17,837,530 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx719,771,322 - 19,799,547 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0721,928,523 - 21,956,738 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0721,710,970 - 21,739,195 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0723,815,246 - 23,843,505 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl723,815,245 - 23,843,634 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0723,964,601 - 23,993,030 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4719,947,498 - 19,975,730 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1719,960,416 - 19,988,648 (-)NCBI
Celera715,042,489 - 15,070,722 (-)NCBICelera
Cytogenetic Map7q13NCBI
Fbxo7
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540541,433,082 - 41,453,909 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540541,429,421 - 41,449,670 (+)NCBIChiLan1.0ChiLan1.0
FBXO7
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22342,411,197 - 42,435,546 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12245,111,484 - 45,135,854 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02213,481,255 - 13,505,301 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12231,335,423 - 31,359,224 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2231,335,423 - 31,359,224 (+)Ensemblpanpan1.1panPan2
FBXO7
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11030,928,059 - 30,948,858 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1030,928,329 - 30,948,977 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1030,910,928 - 30,931,963 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01031,770,136 - 31,791,111 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1031,770,138 - 31,791,130 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11031,510,102 - 31,530,961 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01031,799,411 - 31,820,248 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01031,985,722 - 32,006,997 (-)NCBIUU_Cfam_GSD_1.0
Fbxo7
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494514,251,029 - 14,266,764 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364927,261,009 - 7,276,943 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364927,261,442 - 7,276,779 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FBXO7
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl512,505,654 - 12,526,232 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1512,505,646 - 12,526,206 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2512,291,445 - 12,313,045 (-)NCBISscrofa10.2Sscrofa10.2susScr3
FBXO7
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11915,300,135 - 15,324,256 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1915,300,158 - 15,323,956 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666045110,683,150 - 110,707,342 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Fbxo7
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247501,977,761 - 1,997,231 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247501,977,666 - 1,997,408 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in FBXO7
364 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_012179.4(FBXO7):c.1132C>G (p.Arg378Gly) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000005077] Chr22:32493269 [GRCh38]
Chr22:32889256 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1492C>T (p.Arg498Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000005078]|not provided [RCV002281696] Chr22:32498453 [GRCh38]
Chr22:32894440 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1144+1G>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000005079] Chr22:32493282 [GRCh38]
Chr22:32889269 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.65C>T (p.Thr22Met) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000005080] Chr22:32475067 [GRCh38]
Chr22:32871054 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1264A>T (p.Ile422Phe) single nucleotide variant Inborn genetic diseases [RCV003166548]|Parkinsonian-pyramidal syndrome [RCV001246833] Chr22:32498225 [GRCh38]
Chr22:32894212 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh38/hg38 22q12.1-12.3(chr22:26979579-33992220)x3 copy number gain See cases [RCV000050553] Chr22:26979579..33992220 [GRCh38]
Chr22:27375542..34388209 [GRCh37]
Chr22:25705542..32718209 [NCBI36]
Chr22:22q12.1-12.3		 pathogenic
NM_012179.3(FBXO7):c.968-43C>T single nucleotide variant Malignant melanoma [RCV000063898] Chr22:32493062 [GRCh38]
Chr22:32889049 [GRCh37]
Chr22:31219049 [NCBI36]
Chr22:22q12.3		 not provided
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 copy number gain See cases [RCV000133646] Chr22:16916608..50739836 [GRCh38]
Chr22:17397498..51178264 [GRCh37]
Chr22:15777498..49525130 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
NM_012179.4(FBXO7):c.345G>A (p.Met115Ile) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000616422]|not provided [RCV001610488]|not specified [RCV000175837] Chr22:32479203 [GRCh38]
Chr22:32875190 [GRCh37]
Chr22:22q12.3		 benign
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 copy number gain See cases [RCV000134730] Chr22:16916743..50739785 [GRCh38]
Chr22:17397633..51178213 [GRCh37]
Chr22:15777633..49525079 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3 copy number gain See cases [RCV000138172] Chr22:23279231..36247369 [GRCh38]
Chr22:23621418..36643415 [GRCh37]
Chr22:21951418..34973361 [NCBI36]
Chr22:22q11.23-12.3		 pathogenic
GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3 copy number gain See cases [RCV000137926] Chr22:20907226..37187347 [GRCh38]
Chr22:21261514..37583387 [GRCh37]
Chr22:19591514..35913333 [NCBI36]
Chr22:22q11.21-12.3		 pathogenic
NM_012179.4(FBXO7):c.839T>C (p.Leu280Pro) single nucleotide variant Inborn genetic diseases [RCV002525226]|Parkinsonian-pyramidal syndrome [RCV001858020]|not provided [RCV000519913] Chr22:32487796 [GRCh38]
Chr22:32883783 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 copy number gain See cases [RCV000240091] Chr22:16054691..51237518 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_012179.4(FBXO7):c.1505A>G (p.Asn502Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000263188]|not provided [RCV001573646] Chr22:32498466 [GRCh38]
Chr22:32894453 [GRCh37]
Chr22:22q12.3		 likely benign|uncertain significance
NM_012179.4(FBXO7):c.-93G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000280639] Chr22:32474910 [GRCh38]
Chr22:32870897 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.3(FBXO7):c.-221C>T single nucleotide variant Parkinson Disease, Recessive [RCV000269648]|not provided [RCV001594976] Chr22:32474782 [GRCh38]
Chr22:32870769 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1144+9C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000641221]|not provided [RCV001579859] Chr22:32493290 [GRCh38]
Chr22:32889277 [GRCh37]
Chr22:22q12.3		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_012179.3(FBXO7):c.-268C>G single nucleotide variant Parkinson Disease, Recessive [RCV000309507] Chr22:32474735 [GRCh38]
Chr22:32870722 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.-184C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000274674]|not provided [RCV001653654] Chr22:32474819 [GRCh38]
Chr22:32870806 [GRCh37]
Chr22:22q12.3		 benign|likely benign
NM_012179.4(FBXO7):c.1125A>G (p.Leu375=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000873830]|not provided [RCV002259337] Chr22:32493262 [GRCh38]
Chr22:32889249 [GRCh37]
Chr22:22q12.3		 benign|likely benign|uncertain significance
NM_012179.4(FBXO7):c.949C>T (p.Leu317=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000611094]|not provided [RCV001672611] Chr22:32491163 [GRCh38]
Chr22:32887150 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.425C>G (p.Pro142Arg) single nucleotide variant Parkinson Disease, Recessive [RCV000283154] Chr22:32483904 [GRCh38]
Chr22:32879891 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1527C>A (p.Pro509=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000318405] Chr22:32498488 [GRCh38]
Chr22:32894475 [GRCh37]
Chr22:22q12.3		 conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.122+9G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000531417]|not provided [RCV003221941]|not specified [RCV000592300] Chr22:32475133 [GRCh38]
Chr22:32871120 [GRCh37]
Chr22:22q12.3		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.745A>G (p.Thr249Ala) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000307882] Chr22:32485167 [GRCh38]
Chr22:32881154 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.3(FBXO7):c.*301A>G single nucleotide variant Parkinson Disease, Recessive [RCV000284058] Chr22:32498831 [GRCh38]
Chr22:32894818 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.274G>C (p.Asp92His) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000286438]|not provided [RCV001532462] Chr22:32479132 [GRCh38]
Chr22:32875119 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.*47A>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000354444] Chr22:32498577 [GRCh38]
Chr22:32894564 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.693C>T (p.Ser231=) single nucleotide variant FBXO7-related disorder [RCV003897774]|Parkinsonian-pyramidal syndrome [RCV000552061]|not provided [RCV001310799]|not specified [RCV000591434] Chr22:32485115 [GRCh38]
Chr22:32881102 [GRCh37]
Chr22:22q12.3		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.358C>T (p.Pro120Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000393330] Chr22:32479216 [GRCh38]
Chr22:32875203 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.*170C>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000259495] Chr22:32498700 [GRCh38]
Chr22:32894687 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.540A>G (p.Pro180=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000546312]|not provided [RCV001672610] Chr22:32484019 [GRCh38]
Chr22:32880006 [GRCh37]
Chr22:22q12.3		 benign|likely benign|conflicting interpretations of pathogenicity
NM_012179.4(FBXO7):c.1054G>A (p.Val352Ile) single nucleotide variant Inborn genetic diseases [RCV004021863]|Parkinsonian-pyramidal syndrome [RCV000400945] Chr22:32493191 [GRCh38]
Chr22:32889178 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.260T>C (p.Ile87Thr) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000490301] Chr22:32479118 [GRCh38]
Chr22:32875105 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.-168A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000329836] Chr22:32474835 [GRCh38]
Chr22:32870822 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.3(FBXO7):c.-232G>C single nucleotide variant Parkinson Disease, Recessive [RCV000364231] Chr22:32474771 [GRCh38]
Chr22:32870758 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.49C>G (p.Pro17Ala) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000317019] Chr22:32475051 [GRCh38]
Chr22:32871038 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.3(FBXO7):c.-200G>A single nucleotide variant Parkinson Disease, Recessive [RCV000334060] Chr22:32474803 [GRCh38]
Chr22:32870790 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.3(FBXO7):c.-197C>T single nucleotide variant Parkinson Disease, Recessive [RCV000369298] Chr22:32474806 [GRCh38]
Chr22:32870793 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.*263A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000324196] Chr22:32498793 [GRCh38]
Chr22:32894780 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.-118T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000375116] Chr22:32474885 [GRCh38]
Chr22:32870872 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.*282A>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000378716] Chr22:32498812 [GRCh38]
Chr22:32894799 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.152del (p.Asn51fs) deletion Parkinsonian-pyramidal syndrome [RCV000578350] Chr22:32479009 [GRCh38]
Chr22:32874996 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.601G>A (p.Val201Met) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000641220]|not provided [RCV001546047] Chr22:32484080 [GRCh38]
Chr22:32880067 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1453G>A (p.Val485Ile) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001049233]|not provided [RCV000734164] Chr22:32498414 [GRCh38]
Chr22:32894401 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 copy number gain See cases [RCV000446956] Chr22:16054691..51220902 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_012179.4(FBXO7):c.1530C>T (p.Ser510=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611511]|not specified [RCV000441024] Chr22:32498491 [GRCh38]
Chr22:32894478 [GRCh37]
Chr22:22q12.3		 likely benign
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 copy number gain See cases [RCV000448847] Chr22:16054691..51237463 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.1-12.3(chr22:28349854-33013062)x3 copy number gain See cases [RCV000510523] Chr22:28349854..33013062 [GRCh37]
Chr22:22q12.1-12.3		 likely pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) copy number gain See cases [RCV000510873] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.23-12.3(chr22:23637907-36614412)x3 copy number gain See cases [RCV000511098] Chr22:23637907..36614412 [GRCh37]
Chr22:22q11.23-12.3		 pathogenic
NM_012179.4(FBXO7):c.122+272T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000609047]|not provided [RCV001683608] Chr22:32475396 [GRCh38]
Chr22:32871383 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 copy number gain See cases [RCV000512333] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_012179.4(FBXO7):c.1546G>C (p.Asp516His) single nucleotide variant FBXO7-related disorder [RCV003942668]|Parkinsonian-pyramidal syndrome [RCV000615906]|not provided [RCV000513395] Chr22:32498507 [GRCh38]
Chr22:32894494 [GRCh37]
Chr22:22q12.3		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 22q11.22-12.3(chr22:22460754-35198232)x3 copy number gain not provided [RCV000684530] Chr22:22460754..35198232 [GRCh37]
Chr22:22q11.22-12.3		 pathogenic
NM_012179.4(FBXO7):c.1144+185T>G single nucleotide variant not provided [RCV001544672] Chr22:32493466 [GRCh38]
Chr22:32889453 [GRCh37]
Chr22:22q12.3		 likely benign
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 copy number gain not provided [RCV000741689] Chr22:16054667..51243435 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 copy number gain not provided [RCV000741691] Chr22:16114244..51195728 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 copy number gain not provided [RCV000741692] Chr22:16114244..51211392 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_012179.4(FBXO7):c.1145-156A>G single nucleotide variant not provided [RCV001583051] Chr22:32495337 [GRCh38]
Chr22:32891324 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1145-110_1145-109insCTT insertion not provided [RCV001583062] Chr22:32495381..32495382 [GRCh38]
Chr22:32891368..32891369 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1145-110del deletion not provided [RCV001724533] Chr22:32495369 [GRCh38]
Chr22:32891356 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.417+141del deletion not provided [RCV001612552] Chr22:32479402 [GRCh38]
Chr22:32875389 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1089T>C (p.Phe363=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001471578] Chr22:32493226 [GRCh38]
Chr22:32889213 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.787+182A>G single nucleotide variant not provided [RCV001535264] Chr22:32485391 [GRCh38]
Chr22:32881378 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.*82G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001146785] Chr22:32498612 [GRCh38]
Chr22:32894599 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.*104T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001146786] Chr22:32498634 [GRCh38]
Chr22:32894621 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.11:g.32474600T>C single nucleotide variant not provided [RCV001583277] Chr22:32474600 [GRCh38]
Chr22:32870587 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.646-9G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505145] Chr22:32485059 [GRCh38]
Chr22:32881046 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.303T>C (p.Asn101=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002066262] Chr22:32479161 [GRCh38]
Chr22:32875148 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.522G>A (p.Ser174=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505137] Chr22:32484001 [GRCh38]
Chr22:32879988 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1271T>A (p.Phe424Tyr) single nucleotide variant not provided [RCV000949110] Chr22:32498232 [GRCh38]
Chr22:32894219 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1272C>T (p.Phe424=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611539] Chr22:32498233 [GRCh38]
Chr22:32894220 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1535G>A (p.Gly512Asp) single nucleotide variant Inborn genetic diseases [RCV002539232]|Parkinsonian-pyramidal syndrome [RCV001144824]|not provided [RCV000876905] Chr22:32498496 [GRCh38]
Chr22:32894483 [GRCh37]
Chr22:22q12.3		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.465G>A (p.Ala155=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002502817] Chr22:32483944 [GRCh38]
Chr22:32879931 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1441C>T (p.Arg481Cys) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000945785]|not provided [RCV004783870] Chr22:32498402 [GRCh38]
Chr22:32894389 [GRCh37]
Chr22:22q12.3		 likely benign|uncertain significance
NM_012179.4(FBXO7):c.726_727del (p.Cys243fs) microsatellite FBXO7-related disorder [RCV003392591]|Parkinsonian-pyramidal syndrome [RCV000778655]|not provided [RCV002223936] Chr22:32485144..32485145 [GRCh38]
Chr22:32881131..32881132 [GRCh37]
Chr22:22q12.3		 likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.1268_1272dup (p.Tyr425fs) microsatellite Parkinsonian-pyramidal syndrome [RCV000778656]|not provided [RCV001585706] Chr22:32498222..32498223 [GRCh38]
Chr22:32894209..32894210 [GRCh37]
Chr22:22q12.3		 likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.1271_1272delinsAT (p.Phe424Tyr) indel Parkinsonian-pyramidal syndrome [RCV000874043] Chr22:32498232..32498233 [GRCh38]
Chr22:32894219..32894220 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1183-4del deletion Parkinsonian-pyramidal syndrome [RCV001474113] Chr22:32498140 [GRCh38]
Chr22:32894127 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1009T>C (p.Leu337=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611540] Chr22:32493146 [GRCh38]
Chr22:32889133 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.999C>T (p.Val333=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001398914] Chr22:32493136 [GRCh38]
Chr22:32889123 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.866A>G (p.Lys289Arg) single nucleotide variant Inborn genetic diseases [RCV003248119] Chr22:32487823 [GRCh38]
Chr22:32883810 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1536_1539del (p.Arg513fs) deletion Parkinsonian-pyramidal syndrome [RCV000793915]|not provided [RCV002466584] Chr22:32498495..32498498 [GRCh38]
Chr22:32894482..32894485 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1206_1207dup (p.Arg403fs) duplication Parkinsonian-pyramidal syndrome [RCV000795355]|not provided [RCV002223941] Chr22:32498165..32498166 [GRCh38]
Chr22:32894152..32894153 [GRCh37]
Chr22:22q12.3		 pathogenic|likely pathogenic
NM_012179.4(FBXO7):c.1385G>T (p.Ser462Ile) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000812038]|not provided [RCV001766700] Chr22:32498346 [GRCh38]
Chr22:32894333 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1070C>T (p.Ala357Val) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000808574] Chr22:32493207 [GRCh38]
Chr22:32889194 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.*198T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001146787] Chr22:32498728 [GRCh38]
Chr22:32894715 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.697G>A (p.Val233Met) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV000802923] Chr22:32485119 [GRCh38]
Chr22:32881106 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.291A>C (p.Ser97=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001495702] Chr22:32479149 [GRCh38]
Chr22:32875136 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.169A>G (p.Thr57Ala) single nucleotide variant Inborn genetic diseases [RCV002535891]|Parkinsonian-pyramidal syndrome [RCV000793300] Chr22:32479027 [GRCh38]
Chr22:32875014 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.-130C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001146687] Chr22:32474873 [GRCh38]
Chr22:32870860 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.367T>G (p.Ser123Ala) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001147594] Chr22:32479225 [GRCh38]
Chr22:32875212 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.447G>A (p.Glu149=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001147595] Chr22:32483926 [GRCh38]
Chr22:32879913 [GRCh37]
Chr22:22q12.3		 conflicting interpretations of pathogenicity|uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 copy number gain not provided [RCV000846344] Chr22:16888899..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_012179.4(FBXO7):c.464C>A (p.Ala155Glu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001225456] Chr22:32483943 [GRCh38]
Chr22:32879930 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.403A>T (p.Asn135Tyr) single nucleotide variant not provided [RCV003318070] Chr22:32479261 [GRCh38]
Chr22:32875248 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.155A>G (p.Tyr52Cys) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001147592]|not provided [RCV002225799] Chr22:32479013 [GRCh38]
Chr22:32875000 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1181_1182+1del microsatellite Parkinsonian-pyramidal syndrome [RCV001247770] Chr22:32495526..32495528 [GRCh38]
Chr22:32891513..32891515 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.122+116C>T single nucleotide variant not provided [RCV001673400] Chr22:32475240 [GRCh38]
Chr22:32475240..32475241 [GRCh38]
Chr22:32871227 [GRCh37]
Chr22:32871227..32871228 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.417+141dup duplication not provided [RCV001635956] Chr22:32479401..32479402 [GRCh38]
Chr22:32875388..32875389 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.968-122A>G single nucleotide variant not provided [RCV001555758] Chr22:32492983 [GRCh38]
Chr22:32888970 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.418-267G>T single nucleotide variant not provided [RCV001688630] Chr22:32483630 [GRCh38]
Chr22:32879617 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.645+76G>A single nucleotide variant not provided [RCV001687307] Chr22:32484200 [GRCh38]
Chr22:32880187 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1145-111_1145-110insCT insertion not provided [RCV001643970] Chr22:32495381..32495382 [GRCh38]
Chr22:32891368..32891369 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.968-27C>G single nucleotide variant not provided [RCV001620767] Chr22:32493078 [GRCh38]
Chr22:32889065 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.872-75T>C single nucleotide variant not provided [RCV001719485] Chr22:32491011 [GRCh38]
Chr22:32886998 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.122+555A>G single nucleotide variant not provided [RCV001552450] Chr22:32475679 [GRCh38]
Chr22:32871666 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.213G>A (p.Gly71=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002064750] Chr22:32479071 [GRCh38]
Chr22:32875058 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.319G>A (p.Ala107Thr) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001422015] Chr22:32479177 [GRCh38]
Chr22:32875164 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1506T>C (p.Asn502=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001144823] Chr22:32498467 [GRCh38]
Chr22:32894454 [GRCh37]
Chr22:22q12.3		 conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.-97C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001146688] Chr22:32474906 [GRCh38]
Chr22:32870893 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1221G>A (p.Pro407=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001483333] Chr22:32498182 [GRCh38]
Chr22:32894169 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+343C>G single nucleotide variant not provided [RCV001562683] Chr22:32475467 [GRCh38]
Chr22:32871454 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+119G>T single nucleotide variant not provided [RCV001596725] Chr22:32475243 [GRCh38]
Chr22:32871230 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1144+290C>T single nucleotide variant not provided [RCV001639659] Chr22:32493571 [GRCh38]
Chr22:32889558 [GRCh37]
Chr22:22q12.3		 benign
NC_000022.11:g.32474587A>G single nucleotide variant not provided [RCV001638846] Chr22:32474587 [GRCh38]
Chr22:32870574 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.417+295T>C single nucleotide variant not provided [RCV001678398] Chr22:32479570 [GRCh38]
Chr22:32875557 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3 copy number gain not provided [RCV001007181] Chr22:30654764..51197838 [GRCh37]
Chr22:22q12.2-13.33		 pathogenic
NM_012179.4(FBXO7):c.957T>C (p.Phe319=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001150918] Chr22:32491171 [GRCh38]
Chr22:32887158 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.968-14T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001150919]|not provided [RCV001655685] Chr22:32493091 [GRCh38]
Chr22:32889078 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1266T>G (p.Ile422Met) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001144821] Chr22:32498227 [GRCh38]
Chr22:32894214 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1198C>A (p.His400Asn) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001066527] Chr22:32498159 [GRCh38]
Chr22:32894146 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.728G>C (p.Cys243Ser) single nucleotide variant not provided [RCV001171725] Chr22:32485150 [GRCh38]
Chr22:32881137 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1183-211C>T single nucleotide variant not provided [RCV001610879] Chr22:32497933 [GRCh38]
Chr22:32893920 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.122+382G>A single nucleotide variant not provided [RCV001588777] Chr22:32475506 [GRCh38]
Chr22:32871493 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1182+173T>C single nucleotide variant not provided [RCV001611183] Chr22:32495703 [GRCh38]
Chr22:32891690 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1183-226C>T single nucleotide variant not provided [RCV001710212] Chr22:32497918 [GRCh38]
Chr22:32893905 [GRCh37]
Chr22:22q12.3		 benign
NC_000022.11:g.32474674C>T single nucleotide variant not provided [RCV001707296] Chr22:32474674 [GRCh38]
Chr22:32870661 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.122+254G>A single nucleotide variant not provided [RCV001648362] Chr22:32475378 [GRCh38]
Chr22:32871365 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1145-110dup duplication not provided [RCV001694764] Chr22:32495368..32495369 [GRCh38]
Chr22:32891355..32891356 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.645+32A>G single nucleotide variant not provided [RCV001668704] Chr22:32484156 [GRCh38]
Chr22:32880143 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1183-106T>G single nucleotide variant not provided [RCV001683890] Chr22:32498038 [GRCh38]
Chr22:32894025 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.593C>G (p.Ala198Gly) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001235832] Chr22:32484072 [GRCh38]
Chr22:32880059 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1497C>T (p.Gly499=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001236791] Chr22:32498458 [GRCh38]
Chr22:32894445 [GRCh37]
Chr22:22q12.3		 likely benign|uncertain significance
NM_012179.4(FBXO7):c.1332C>G (p.Ile444Met) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001144822] Chr22:32498293 [GRCh38]
Chr22:32894280 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1552C>T (p.Arg518Trp) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001146784]|not provided [RCV004694911] Chr22:32498513 [GRCh38]
Chr22:32894500 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.277T>G (p.Ser93Ala) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001147593] Chr22:32479135 [GRCh38]
Chr22:32875122 [GRCh37]
Chr22:22q12.3		 conflicting interpretations of pathogenicity|uncertain significance
NM_012179.4(FBXO7):c.32C>T (p.Thr11Ile) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001203007] Chr22:32475034 [GRCh38]
Chr22:32871021 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3 copy number gain See cases [RCV001263056] Chr22:16197005..51224252 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_012179.4(FBXO7):c.1312C>T (p.Arg438Cys) single nucleotide variant Inborn genetic diseases [RCV002570643]|Parkinsonian-pyramidal syndrome [RCV002032519]|not provided [RCV001540091] Chr22:32498273 [GRCh38]
Chr22:32894260 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.11:g.32503839_32503840insACGCCCCAACCTCTTATCTCTGCGCCCCAATCGCTTATTTCC insertion not provided [RCV001354305] Chr22:32503824..32503825 [GRCh38]
Chr22:32899811..32899812 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.11:g.32500544C>T single nucleotide variant not provided [RCV001355638] Chr22:32500544 [GRCh38]
Chr22:32896531 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.11:g.32500543_32500544insGTTTTTTTTTTT insertion not provided [RCV001354321] Chr22:32500543..32500544 [GRCh38]
Chr22:32896530..32896531 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1546G>T (p.Asp516Tyr) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001340077] Chr22:32498507 [GRCh38]
Chr22:32894494 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.11:g.32502021T>C single nucleotide variant not provided [RCV001354334] Chr22:32502021 [GRCh38]
Chr22:32898008 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.11:g.32500544delinsGTTTTTTTTTTTT indel not provided [RCV001354433] Chr22:32500544 [GRCh38]
Chr22:32896531 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1086C>T (p.Leu362=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001401961] Chr22:32493223 [GRCh38]
Chr22:32889210 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.872-288C>T single nucleotide variant not provided [RCV001675295] Chr22:32490798 [GRCh38]
Chr22:32886785 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.418-7T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001457798] Chr22:32483890 [GRCh38]
Chr22:32879877 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.123-10T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001482804] Chr22:32478971 [GRCh38]
Chr22:32874958 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1145-8C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001473873] Chr22:32495485 [GRCh38]
Chr22:32891472 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.871+221T>A single nucleotide variant not provided [RCV001715706] Chr22:32488049 [GRCh38]
Chr22:32884036 [GRCh37]
Chr22:22q12.3		 benign
NC_000022.11:g.32474434G>A single nucleotide variant not provided [RCV001590007] Chr22:32474434 [GRCh38]
Chr22:32870421 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+331C>A single nucleotide variant not provided [RCV001616918] Chr22:32475455 [GRCh38]
Chr22:32871442 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.993G>T (p.Gly331=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001463195] Chr22:32493130 [GRCh38]
Chr22:32889117 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.646-10C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001452468] Chr22:32485058 [GRCh38]
Chr22:32881045 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1495G>A (p.Gly499Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001495246]|not provided [RCV002225839] Chr22:32498456 [GRCh38]
Chr22:32894443 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.803A>G (p.Asn268Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002032754]|not provided [RCV001754284] Chr22:32487760 [GRCh38]
Chr22:32883747 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1037T>A (p.Leu346His) single nucleotide variant not provided [RCV001764905] Chr22:32493174 [GRCh38]
Chr22:32889161 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.674C>T (p.Pro225Leu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001733646] Chr22:32485096 [GRCh38]
Chr22:32881083 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.992G>T (p.Gly331Val) single nucleotide variant not provided [RCV001754023] Chr22:32493129 [GRCh38]
Chr22:32889116 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1145-7T>C single nucleotide variant not provided [RCV001816321] Chr22:32495486 [GRCh38]
Chr22:32891473 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1453G>C (p.Val485Leu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001929146] Chr22:32498414 [GRCh38]
Chr22:32894401 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.917G>A (p.Arg306His) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002005972]|not provided [RCV004694086] Chr22:32491131 [GRCh38]
Chr22:32887118 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1386T>G (p.Ser462Arg) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002045332] Chr22:32498347 [GRCh38]
Chr22:32894334 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1490G>C (p.Gly497Ala) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002003088] Chr22:32498451 [GRCh38]
Chr22:32894438 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.114G>C (p.Trp38Cys) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001974108] Chr22:32475116 [GRCh38]
Chr22:32871103 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.521C>T (p.Ser174Leu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001956029] Chr22:32484000 [GRCh38]
Chr22:32879987 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1553G>A (p.Arg518Gln) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001931832] Chr22:32498514 [GRCh38]
Chr22:32894501 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.10:g.(?_29083885)_(34046674_?)dup duplication not provided [RCV001979643] Chr22:29083885..34046674 [GRCh37]
Chr22:22q12.1-12.3		 uncertain significance
NM_012179.4(FBXO7):c.430C>G (p.Gln144Glu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002010321] Chr22:32483909 [GRCh38]
Chr22:32879896 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1541del (p.Pro514fs) deletion Parkinsonian-pyramidal syndrome [RCV001975270] Chr22:32498501 [GRCh38]
Chr22:32894488 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.284A>T (p.His95Leu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001979226] Chr22:32479142 [GRCh38]
Chr22:32875129 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.661G>C (p.Ala221Pro) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001955758] Chr22:32485083 [GRCh38]
Chr22:32881070 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1213G>T (p.Glu405Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001950804] Chr22:32498174 [GRCh38]
Chr22:32894161 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.364G>A (p.Asp122Asn) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001881867] Chr22:32479222 [GRCh38]
Chr22:32875209 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.10:g.(?_32232938)_(34157463_?)dup duplication Muscular dystrophy-dystroglycanopathy type B6 [RCV001920547] Chr22:32232938..34157463 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.571G>C (p.Asp191His) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV001932011] Chr22:32484050 [GRCh38]
Chr22:32880037 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1100A>G (p.Asn367Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002034282] Chr22:32493237 [GRCh38]
Chr22:32889224 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.10:g.(?_32870990)_(32875282_?)dup duplication Parkinsonian-pyramidal syndrome [RCV001939145] Chr22:32870990..32875282 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1388C>T (p.Ser463Leu) single nucleotide variant Inborn genetic diseases [RCV003348653]|Parkinsonian-pyramidal syndrome [RCV001960140] Chr22:32498349 [GRCh38]
Chr22:32894336 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.674C>G (p.Pro225Arg) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002050727] Chr22:32485096 [GRCh38]
Chr22:32881083 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.899A>T (p.Asp300Val) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002015727] Chr22:32491113 [GRCh38]
Chr22:32887100 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1182+18T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002112065] Chr22:32495548 [GRCh38]
Chr22:32891535 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.961C>T (p.Arg321Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003101279]|not provided [RCV002224946] Chr22:32491175 [GRCh38]
Chr22:32887162 [GRCh37]
Chr22:22q12.3		 pathogenic|likely pathogenic
NM_012179.4(FBXO7):c.110C>G (p.Thr37Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002191504] Chr22:32475112 [GRCh38]
Chr22:32871099 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.871+15_871+17del microsatellite Parkinsonian-pyramidal syndrome [RCV002212407] Chr22:32487840..32487842 [GRCh38]
Chr22:32883827..32883829 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.306G>A (p.Glu102=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002170880] Chr22:32479164 [GRCh38]
Chr22:32875151 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-15T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002081893] Chr22:32498129 [GRCh38]
Chr22:32894116 [GRCh37]
Chr22:22q12.3		 likely benign
NC_000022.10:g.(?_32500753)_(32894517_?)dup duplication Congenital glucose-galactose malabsorption [RCV003111075] Chr22:32500753..32894517 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1033C>T (p.Arg345Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003123290]|not provided [RCV004721153] Chr22:32493170 [GRCh38]
Chr22:32889157 [GRCh37]
Chr22:22q12.3		 pathogenic|likely pathogenic
NM_012179.4(FBXO7):c.1345_1347delinsTAA (p.Asp449Ter) indel Parkinsonian-pyramidal syndrome [RCV002226951] Chr22:32498306..32498308 [GRCh38]
Chr22:32894293..32894295 [GRCh37]
Chr22:22q12.3		 likely pathogenic
NM_012179.4(FBXO7):c.542A>G (p.His181Arg) single nucleotide variant not provided [RCV002276107] Chr22:32484021 [GRCh38]
Chr22:32880008 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.686A>G (p.Lys229Arg) single nucleotide variant Inborn genetic diseases [RCV002728093] Chr22:32485108 [GRCh38]
Chr22:32881095 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.256A>G (p.Asn86Asp) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002908772] Chr22:32479114 [GRCh38]
Chr22:32875101 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1079G>A (p.Arg360His) single nucleotide variant Inborn genetic diseases [RCV002689320] Chr22:32493216 [GRCh38]
Chr22:32889203 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.629C>T (p.Ser210Leu) single nucleotide variant Inborn genetic diseases [RCV002778403] Chr22:32484108 [GRCh38]
Chr22:32880095 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.812T>C (p.Ile271Thr) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003076091] Chr22:32487769 [GRCh38]
Chr22:32883756 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.195A>G (p.Ser65=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002885464] Chr22:32479053 [GRCh38]
Chr22:32875040 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1460C>T (p.Pro487Leu) single nucleotide variant Inborn genetic diseases [RCV002661300] Chr22:32498421 [GRCh38]
Chr22:32894408 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1048C>T (p.Arg350Cys) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002912496] Chr22:32493185 [GRCh38]
Chr22:32889172 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.400T>G (p.Trp134Gly) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002781118] Chr22:32479258 [GRCh38]
Chr22:32875245 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.555C>T (p.Thr185=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003000090] Chr22:32484034 [GRCh38]
Chr22:32880021 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.652G>A (p.Glu218Lys) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002885897] Chr22:32485074 [GRCh38]
Chr22:32881061 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.912C>T (p.Leu304=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002952472] Chr22:32491126 [GRCh38]
Chr22:32887113 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1537C>T (p.Arg513Trp) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002909471] Chr22:32498498 [GRCh38]
Chr22:32894485 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.122+3A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003021007] Chr22:32475127 [GRCh38]
Chr22:32871114 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.185C>A (p.Thr62Asn) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002760440] Chr22:32479043 [GRCh38]
Chr22:32875030 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.944C>T (p.Pro315Leu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002795699] Chr22:32491158 [GRCh38]
Chr22:32887145 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1566G>C (p.Met522Ile) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002913603] Chr22:32498527 [GRCh38]
Chr22:32894514 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.437T>C (p.Phe146Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003058500] Chr22:32483916 [GRCh38]
Chr22:32879903 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.330C>T (p.Ser110=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002985662] Chr22:32479188 [GRCh38]
Chr22:32875175 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1218C>T (p.Ser406=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002700840] Chr22:32498179 [GRCh38]
Chr22:32894166 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1262C>T (p.Thr421Ile) single nucleotide variant Inborn genetic diseases [RCV002919724] Chr22:32498223 [GRCh38]
Chr22:32894210 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.521C>A (p.Ser174Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002876753] Chr22:32484000 [GRCh38]
Chr22:32879987 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1183C>T (p.Leu395=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002626879] Chr22:32498144 [GRCh38]
Chr22:32894131 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.455A>C (p.Gln152Pro) single nucleotide variant Inborn genetic diseases [RCV002826260] Chr22:32483934 [GRCh38]
Chr22:32879921 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1309T>A (p.Ser437Thr) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002982875] Chr22:32498270 [GRCh38]
Chr22:32894257 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.587A>G (p.Asn196Ser) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002573853] Chr22:32484066 [GRCh38]
Chr22:32880053 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.580G>A (p.Asp194Asn) single nucleotide variant Inborn genetic diseases [RCV002891525] Chr22:32484059 [GRCh38]
Chr22:32880046 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.665T>G (p.Leu222Arg) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002663812] Chr22:32485087 [GRCh38]
Chr22:32881074 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.595T>C (p.Leu199=) single nucleotide variant FBXO7-related disorder [RCV003933806]|Parkinsonian-pyramidal syndrome [RCV002580945] Chr22:32484074 [GRCh38]
Chr22:32880061 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1082A>G (p.Asp361Gly) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002647680] Chr22:32493219 [GRCh38]
Chr22:32889206 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.349G>T (p.Asp117Tyr) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002716961] Chr22:32479207 [GRCh38]
Chr22:32875194 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.127A>G (p.Asn43Asp) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002629908] Chr22:32478985 [GRCh38]
Chr22:32874972 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.251C>T (p.Ala84Val) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002648109] Chr22:32479109 [GRCh38]
Chr22:32875096 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.968-17T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003061394] Chr22:32493088 [GRCh38]
Chr22:32889075 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.417+18A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002584393] Chr22:32479293 [GRCh38]
Chr22:32875280 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.911T>A (p.Leu304His) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV002635137] Chr22:32491125 [GRCh38]
Chr22:32887112 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.269_270del (p.Ser90fs) deletion Parkinsonian-pyramidal syndrome [RCV003071818] Chr22:32479127..32479128 [GRCh38]
Chr22:32875114..32875115 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1049G>A (p.Arg350His) single nucleotide variant not provided [RCV004790874] Chr22:32493186 [GRCh38]
Chr22:32889173 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1078C>T (p.Arg360Cys) single nucleotide variant Inborn genetic diseases [RCV003256786] Chr22:32493215 [GRCh38]
Chr22:32889202 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.529G>A (p.Gly177Arg) single nucleotide variant Inborn genetic diseases [RCV003200712] Chr22:32484008 [GRCh38]
Chr22:32879995 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1347C>G (p.Asp449Glu) single nucleotide variant Inborn genetic diseases [RCV003218081] Chr22:32498308 [GRCh38]
Chr22:32894295 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.482C>G (p.Thr161Arg) single nucleotide variant Inborn genetic diseases [RCV003196335] Chr22:32483961 [GRCh38]
Chr22:32879948 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.52G>A (p.Glu18Lys) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003337907] Chr22:32475054 [GRCh38]
Chr22:32871041 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.491A>G (p.Tyr164Cys) single nucleotide variant not provided [RCV003334245] Chr22:32483970 [GRCh38]
Chr22:32879957 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.692G>A (p.Ser231Asn) single nucleotide variant Inborn genetic diseases [RCV003344642] Chr22:32485114 [GRCh38]
Chr22:32881101 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1429C>T (p.Pro477Ser) single nucleotide variant Inborn genetic diseases [RCV003364255] Chr22:32498390 [GRCh38]
Chr22:32894377 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.787+13C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506080] Chr22:32485222 [GRCh38]
Chr22:32881209 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.622T>C (p.Leu208=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505439] Chr22:32484101 [GRCh38]
Chr22:32880088 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1380A>G (p.Pro460=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504907] Chr22:32498341 [GRCh38]
Chr22:32894328 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.123-20T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505480] Chr22:32478961 [GRCh38]
Chr22:32874948 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.872-15T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506311] Chr22:32491071 [GRCh38]
Chr22:32887058 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.788-15T>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506318] Chr22:32487730 [GRCh38]
Chr22:32883717 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+13C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506322] Chr22:32475137 [GRCh38]
Chr22:32871124 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.603G>A (p.Val201=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003873310] Chr22:32484082 [GRCh38]
Chr22:32880069 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.788-11T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505506] Chr22:32487734 [GRCh38]
Chr22:32883721 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-2_1183-1del deletion Parkinsonian-pyramidal syndrome [RCV003505802] Chr22:32498142..32498143 [GRCh38]
Chr22:32894129..32894130 [GRCh37]
Chr22:22q12.3		 likely pathogenic
NM_012179.4(FBXO7):c.575_576del (p.Cys192fs) deletion Parkinsonian-pyramidal syndrome [RCV003505531] Chr22:32484053..32484054 [GRCh38]
Chr22:32880040..32880041 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.252G>A (p.Ala84=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506207] Chr22:32479110 [GRCh38]
Chr22:32875097 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.174A>C (p.Gly58=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505569] Chr22:32479032 [GRCh38]
Chr22:32875019 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.909A>G (p.Lys303=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505577] Chr22:32491123 [GRCh38]
Chr22:32887110 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-11T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504613] Chr22:32498133 [GRCh38]
Chr22:32894120 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.384A>G (p.Ala128=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505041] Chr22:32479242 [GRCh38]
Chr22:32875229 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.418-1G>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505042] Chr22:32483896 [GRCh38]
Chr22:32879883 [GRCh37]
Chr22:22q12.3		 likely pathogenic
NM_012179.4(FBXO7):c.497C>G (p.Ser166Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504783] Chr22:32483976 [GRCh38]
Chr22:32879963 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1419C>T (p.Ser473=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506100] Chr22:32498380 [GRCh38]
Chr22:32894367 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.788-16_788-13del deletion Parkinsonian-pyramidal syndrome [RCV003506181] Chr22:32487729..32487732 [GRCh38]
Chr22:32883716..32883719 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.33C>T (p.Thr11=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504674] Chr22:32475035 [GRCh38]
Chr22:32871022 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.564_567del (p.Ser189fs) microsatellite Parkinsonian-pyramidal syndrome [RCV003505073] Chr22:32484039..32484042 [GRCh38]
Chr22:32880026..32880029 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.872-19A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505622] Chr22:32491067 [GRCh38]
Chr22:32887054 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+14G>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505637] Chr22:32475138 [GRCh38]
Chr22:32871125 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.564A>G (p.Gln188=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505939] Chr22:32484043 [GRCh38]
Chr22:32880030 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.417+20A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506192] Chr22:32479295 [GRCh38]
Chr22:32875282 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.48G>A (p.Val16=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506208] Chr22:32475050 [GRCh38]
Chr22:32871037 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.40C>T (p.Leu14=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506214] Chr22:32475042 [GRCh38]
Chr22:32871029 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.651C>T (p.Thr217=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506220] Chr22:32485073 [GRCh38]
Chr22:32881060 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1A>G (p.Met1Val) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504782] Chr22:32475003 [GRCh38]
Chr22:32870990 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1362T>C (p.Leu454=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504801] Chr22:32498323 [GRCh38]
Chr22:32894310 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1236G>A (p.Val412=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505651] Chr22:32498197 [GRCh38]
Chr22:32894184 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1145-9C>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504687] Chr22:32495484 [GRCh38]
Chr22:32891471 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.787+17G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505953] Chr22:32485226 [GRCh38]
Chr22:32881213 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.921C>T (p.Leu307=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506237] Chr22:32491135 [GRCh38]
Chr22:32887122 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.645+22_645+23del microsatellite Parkinsonian-pyramidal syndrome [RCV003506244] Chr22:32484143..32484144 [GRCh38]
Chr22:32880130..32880131 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1188C>A (p.Tyr396Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003504819] Chr22:32498149 [GRCh38]
Chr22:32894136 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.544dup (p.Ser182fs) duplication Parkinsonian-pyramidal syndrome [RCV003504908] Chr22:32484021..32484022 [GRCh38]
Chr22:32880008..32880009 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.122+10G>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505991] Chr22:32475134 [GRCh38]
Chr22:32871121 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.646-20C>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505348] Chr22:32485048 [GRCh38]
Chr22:32881035 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.537G>A (p.Val179=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505370] Chr22:32484016 [GRCh38]
Chr22:32880003 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.120C>T (p.Tyr40=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003505382] Chr22:32475122 [GRCh38]
Chr22:32871109 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.156C>G (p.Tyr52Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506293] Chr22:32479014 [GRCh38]
Chr22:32875001 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.418-11T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506040] Chr22:32483886 [GRCh38]
Chr22:32879873 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1220del (p.Pro407fs) deletion Parkinsonian-pyramidal syndrome [RCV003506057] Chr22:32498178 [GRCh38]
Chr22:32894165 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.30G>A (p.Arg10=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506153] Chr22:32475032 [GRCh38]
Chr22:32871019 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1413G>A (p.Thr471=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003825609] Chr22:32498374 [GRCh38]
Chr22:32894361 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.133C>T (p.Arg45Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003441156] Chr22:32478991 [GRCh38]
Chr22:32874978 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.146C>A (p.Thr49Lys) single nucleotide variant not provided [RCV003480386] Chr22:32479004 [GRCh38]
Chr22:32874991 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.719A>C (p.His240Pro) single nucleotide variant not provided [RCV003480387] Chr22:32485141 [GRCh38]
Chr22:32881128 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.4A>C (p.Arg2=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611649]|not provided [RCV003437540] Chr22:32475006 [GRCh38]
Chr22:32870993 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.131C>A (p.Thr44Asn) single nucleotide variant FBXO7-related disorder [RCV003402753] Chr22:32478989 [GRCh38]
Chr22:32874976 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.417+7A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003879147] Chr22:32479282 [GRCh38]
Chr22:32875269 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.666G>C (p.Leu222=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003831828] Chr22:32485088 [GRCh38]
Chr22:32881075 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.741C>T (p.Ser247=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003849196] Chr22:32485163 [GRCh38]
Chr22:32881150 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1451del (p.Pro484fs) deletion Parkinsonian-pyramidal syndrome [RCV003831257] Chr22:32498411 [GRCh38]
Chr22:32894398 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.788-12_788-9del deletion Parkinsonian-pyramidal syndrome [RCV003506392] Chr22:32487730..32487733 [GRCh38]
Chr22:32883717..32883720 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.915_916del (p.Arg306fs) microsatellite Parkinsonian-pyramidal syndrome [RCV003506489] Chr22:32491124..32491125 [GRCh38]
Chr22:32887111..32887112 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.117G>T (p.Gly39=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506662] Chr22:32475119 [GRCh38]
Chr22:32871106 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1497C>A (p.Gly499=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506667] Chr22:32498458 [GRCh38]
Chr22:32894445 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1182+7A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506712] Chr22:32495537 [GRCh38]
Chr22:32891524 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.408C>T (p.Asp136=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506733] Chr22:32479266 [GRCh38]
Chr22:32875253 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-20T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003824830] Chr22:32498124 [GRCh38]
Chr22:32894111 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.418-16T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506363] Chr22:32483881 [GRCh38]
Chr22:32879868 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.709C>T (p.Gln237Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506507] Chr22:32485131 [GRCh38]
Chr22:32881118 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1145-14C>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506446] Chr22:32495479 [GRCh38]
Chr22:32891466 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.462T>C (p.Asn154=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506500] Chr22:32483941 [GRCh38]
Chr22:32879928 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1494A>G (p.Arg498=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003882691] Chr22:32498455 [GRCh38]
Chr22:32894442 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.967+18G>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506616] Chr22:32491199 [GRCh38]
Chr22:32887186 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1251G>A (p.Ser417=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003878477] Chr22:32498212 [GRCh38]
Chr22:32894199 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.729C>T (p.Cys243=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003878533] Chr22:32485151 [GRCh38]
Chr22:32881138 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.378A>G (p.Gly126=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003876999] Chr22:32479236 [GRCh38]
Chr22:32875223 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.872-7A>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003825965] Chr22:32491079 [GRCh38]
Chr22:32887066 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.573C>T (p.Asp191=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506333] Chr22:32484052 [GRCh38]
Chr22:32880039 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.100C>T (p.Leu34=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506359] Chr22:32475102 [GRCh38]
Chr22:32871089 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.970C>T (p.Leu324=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506353] Chr22:32493107 [GRCh38]
Chr22:32889094 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1236G>T (p.Val412=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506413] Chr22:32498197 [GRCh38]
Chr22:32894184 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.135A>G (p.Arg45=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506715] Chr22:32478993 [GRCh38]
Chr22:32874980 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-9T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003506728] Chr22:32498135 [GRCh38]
Chr22:32894122 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1416C>T (p.Pro472=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003811737] Chr22:32498377 [GRCh38]
Chr22:32894364 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1A>C (p.Met1Leu) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611390] Chr22:32475003 [GRCh38]
Chr22:32870990 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.2T>G (p.Met1Arg) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612416] Chr22:32475004 [GRCh38]
Chr22:32870991 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.744T>C (p.Ala248=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003850340] Chr22:32485166 [GRCh38]
Chr22:32881153 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1308C>T (p.Ser436=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612580] Chr22:32498269 [GRCh38]
Chr22:32894256 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1145-8del deletion Parkinsonian-pyramidal syndrome [RCV003612609] Chr22:32495484 [GRCh38]
Chr22:32891471 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1467A>G (p.Pro489=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611755] Chr22:32498428 [GRCh38]
Chr22:32894415 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.546A>G (p.Ser182=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611772] Chr22:32484025 [GRCh38]
Chr22:32880012 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.45G>A (p.Glu15=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613017] Chr22:32475047 [GRCh38]
Chr22:32871034 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.873G>A (p.Gly291=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613023] Chr22:32491087 [GRCh38]
Chr22:32887074 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+7dup duplication Parkinsonian-pyramidal syndrome [RCV003611912] Chr22:32475130..32475131 [GRCh38]
Chr22:32871117..32871118 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.788-8A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611959] Chr22:32487737 [GRCh38]
Chr22:32883724 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1371T>G (p.Val457=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613110] Chr22:32498332 [GRCh38]
Chr22:32894319 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.465G>T (p.Ala155=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612026] Chr22:32483944 [GRCh38]
Chr22:32879931 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.792A>G (p.Thr264=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003833275] Chr22:32487749 [GRCh38]
Chr22:32883736 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.354A>G (p.Glu118=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612022] Chr22:32479212 [GRCh38]
Chr22:32875199 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.821_822del (p.Val274fs) microsatellite Parkinsonian-pyramidal syndrome [RCV003612085] Chr22:32487775..32487776 [GRCh38]
Chr22:32883762..32883763 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1144+10G>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613231] Chr22:32493291 [GRCh38]
Chr22:32889278 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-7T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612160] Chr22:32498137 [GRCh38]
Chr22:32894124 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.872-9dup duplication Parkinsonian-pyramidal syndrome [RCV003613298] Chr22:32491071..32491072 [GRCh38]
Chr22:32887058..32887059 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.249A>G (p.Pro83=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612051] Chr22:32479107 [GRCh38]
Chr22:32875094 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.579T>C (p.Ser193=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612208] Chr22:32484058 [GRCh38]
Chr22:32880045 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.917_918del (p.Arg306fs) deletion Parkinsonian-pyramidal syndrome [RCV003612254] Chr22:32491130..32491131 [GRCh38]
Chr22:32887117..32887118 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.345G>C (p.Met115Ile) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612219] Chr22:32479203 [GRCh38]
Chr22:32875190 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1144+10G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612228] Chr22:32493291 [GRCh38]
Chr22:32889278 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.788-15_788-13del deletion Parkinsonian-pyramidal syndrome [RCV003613416] Chr22:32487729..32487731 [GRCh38]
Chr22:32883716..32883718 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.872-4C>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611073] Chr22:32491082 [GRCh38]
Chr22:32887069 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.967+14T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612296] Chr22:32491195 [GRCh38]
Chr22:32887182 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1470A>G (p.Gly490=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611049] Chr22:32498431 [GRCh38]
Chr22:32894418 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1368T>C (p.Tyr456=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612279] Chr22:32498329 [GRCh38]
Chr22:32894316 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1141C>T (p.Arg381Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612314] Chr22:32493278 [GRCh38]
Chr22:32889265 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1053C>T (p.Ser351=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611189] Chr22:32493190 [GRCh38]
Chr22:32889177 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.987A>G (p.Val329=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611106] Chr22:32493124 [GRCh38]
Chr22:32889111 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.418-2A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612368] Chr22:32483895 [GRCh38]
Chr22:32879882 [GRCh37]
Chr22:22q12.3		 likely pathogenic
NM_012179.4(FBXO7):c.411C>T (p.Asp137=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611217] Chr22:32479269 [GRCh38]
Chr22:32875256 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1392C>T (p.Leu464=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611441] Chr22:32498353 [GRCh38]
Chr22:32894340 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.925A>T (p.Lys309Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613205] Chr22:32491139 [GRCh38]
Chr22:32887126 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.787+11A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611482] Chr22:32485220 [GRCh38]
Chr22:32881207 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1182+12T>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003832882] Chr22:32495542 [GRCh38]
Chr22:32891529 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.645+19A>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612152] Chr22:32484143 [GRCh38]
Chr22:32880130 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1365C>G (p.Pro455=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613283] Chr22:32498326 [GRCh38]
Chr22:32894313 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+17G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003856007] Chr22:32475141 [GRCh38]
Chr22:32871128 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.879T>C (p.Asn293=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613379] Chr22:32491093 [GRCh38]
Chr22:32887080 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.894C>T (p.Tyr298=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003817176] Chr22:32491108 [GRCh38]
Chr22:32887095 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.432A>G (p.Gln144=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611137] Chr22:32483911 [GRCh38]
Chr22:32879898 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.72G>A (p.Gly24=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612319] Chr22:32475074 [GRCh38]
Chr22:32871061 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.123-12C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612888] Chr22:32478969 [GRCh38]
Chr22:32874956 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1215A>G (p.Glu405=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611179] Chr22:32498176 [GRCh38]
Chr22:32894163 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.788-9dup duplication Parkinsonian-pyramidal syndrome [RCV003612356] Chr22:32487733..32487734 [GRCh38]
Chr22:32883720..32883721 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.645+12A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612366] Chr22:32484136 [GRCh38]
Chr22:32880123 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.316_317del (p.Leu106fs) deletion Parkinsonian-pyramidal syndrome [RCV003612947] Chr22:32479173..32479174 [GRCh38]
Chr22:32875160..32875161 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.645+13A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612403] Chr22:32484137 [GRCh38]
Chr22:32880124 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-19_1183-16del deletion Parkinsonian-pyramidal syndrome [RCV003612992] Chr22:32498122..32498125 [GRCh38]
Chr22:32894109..32894112 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.426T>C (p.Pro142=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611245] Chr22:32483905 [GRCh38]
Chr22:32879892 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1155C>G (p.Val385=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612453] Chr22:32495503 [GRCh38]
Chr22:32891490 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.156C>T (p.Tyr52=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611256] Chr22:32479014 [GRCh38]
Chr22:32875001 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1491G>A (p.Gly497=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611266] Chr22:32498452 [GRCh38]
Chr22:32894439 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.377del (p.Gly126fs) deletion Parkinsonian-pyramidal syndrome [RCV003611338] Chr22:32479234 [GRCh38]
Chr22:32875221 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1183-7del deletion Parkinsonian-pyramidal syndrome [RCV003611363] Chr22:32498132 [GRCh38]
Chr22:32894119 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.468T>C (p.His156=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612427] Chr22:32483947 [GRCh38]
Chr22:32879934 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.788-17_788-13del deletion Parkinsonian-pyramidal syndrome [RCV003839541] Chr22:32487725..32487729 [GRCh38]
Chr22:32883712..32883716 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1062T>G (p.Ser354=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611381] Chr22:32493199 [GRCh38]
Chr22:32889186 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.967+9T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611384] Chr22:32491190 [GRCh38]
Chr22:32887177 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.393T>C (p.Ser131=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611696] Chr22:32479251 [GRCh38]
Chr22:32875238 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.2T>A (p.Met1Lys) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003817422] Chr22:32475004 [GRCh38]
Chr22:32870991 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.123-20T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613353] Chr22:32478961 [GRCh38]
Chr22:32874948 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.968-18C>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613403] Chr22:32493087 [GRCh38]
Chr22:32889074 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1248A>G (p.Pro416=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613464] Chr22:32498209 [GRCh38]
Chr22:32894196 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.978A>G (p.Leu326=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612263] Chr22:32493115 [GRCh38]
Chr22:32889102 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1145-20T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611115] Chr22:32495473 [GRCh38]
Chr22:32891460 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1041G>A (p.Leu347=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003851108] Chr22:32493178 [GRCh38]
Chr22:32889165 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1408G>T (p.Glu470Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612402] Chr22:32498369 [GRCh38]
Chr22:32894356 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.846A>G (p.Glu282=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003855906] Chr22:32487803 [GRCh38]
Chr22:32883790 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.801C>A (p.Ile267=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611289] Chr22:32487758 [GRCh38]
Chr22:32883745 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1314C>T (p.Arg438=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611417] Chr22:32498275 [GRCh38]
Chr22:32894262 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.33C>G (p.Thr11=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611478] Chr22:32475035 [GRCh38]
Chr22:32871022 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.893_894insT (p.Lys299fs) insertion Parkinsonian-pyramidal syndrome [RCV003815200] Chr22:32491107..32491108 [GRCh38]
Chr22:32887094..32887095 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.630A>G (p.Ser210=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003833123] Chr22:32484109 [GRCh38]
Chr22:32880096 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.968-9T>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612896] Chr22:32493096 [GRCh38]
Chr22:32889083 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.531G>A (p.Gly177=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611082] Chr22:32484010 [GRCh38]
Chr22:32879997 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1344T>A (p.Tyr448Ter) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611934] Chr22:32498305 [GRCh38]
Chr22:32894292 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.1269A>G (p.Pro423=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612112] Chr22:32498230 [GRCh38]
Chr22:32894217 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.787+14A>G single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612114] Chr22:32485223 [GRCh38]
Chr22:32881210 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.444T>C (p.Ala148=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612196] Chr22:32483923 [GRCh38]
Chr22:32879910 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1183-10T>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003613303] Chr22:32498134 [GRCh38]
Chr22:32894121 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1221G>T (p.Pro407=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611812] Chr22:32498182 [GRCh38]
Chr22:32894169 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1299A>G (p.Pro433=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611161] Chr22:32498260 [GRCh38]
Chr22:32894247 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.968-10_968-9del deletion Parkinsonian-pyramidal syndrome [RCV003611186] Chr22:32493090..32493091 [GRCh38]
Chr22:32889077..32889078 [GRCh37]
Chr22:22q12.3		 benign
NM_012179.4(FBXO7):c.1476C>T (p.Asn492=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611885] Chr22:32498437 [GRCh38]
Chr22:32894424 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1071G>A (p.Ala357=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003612441] Chr22:32493208 [GRCh38]
Chr22:32889195 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.646-15C>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611937] Chr22:32485053 [GRCh38]
Chr22:32881040 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.122+16G>A single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003611942] Chr22:32475140 [GRCh38]
Chr22:32871127 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1144+19T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003845482] Chr22:32493300 [GRCh38]
Chr22:32889287 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.675G>A (p.Pro225=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003819219] Chr22:32485097 [GRCh38]
Chr22:32881084 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1278C>T (p.Pro426=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003870978] Chr22:32498239 [GRCh38]
Chr22:32894226 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.967+17T>C single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003869384] Chr22:32491198 [GRCh38]
Chr22:32887185 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1302T>C (p.Phe434=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003871451] Chr22:32498263 [GRCh38]
Chr22:32894250 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.969A>G (p.Ala323=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003871833] Chr22:32493106 [GRCh38]
Chr22:32889093 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.90G>A (p.Leu30=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003848458] Chr22:32475092 [GRCh38]
Chr22:32871079 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.795A>G (p.Leu265=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003869603] Chr22:32487752 [GRCh38]
Chr22:32883739 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.930C>T (p.Asp310=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003866421] Chr22:32491144 [GRCh38]
Chr22:32887131 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.84G>A (p.Ser28=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003820546] Chr22:32475086 [GRCh38]
Chr22:32871073 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.968-16_968-14del deletion Parkinsonian-pyramidal syndrome [RCV003861733] Chr22:32493088..32493090 [GRCh38]
Chr22:32889075..32889077 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1026G>C (p.Arg342=) single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003847302] Chr22:32493163 [GRCh38]
Chr22:32889150 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.418-2A>T single nucleotide variant Parkinsonian-pyramidal syndrome [RCV003819303] Chr22:32483895 [GRCh38]
Chr22:32879882 [GRCh37]
Chr22:22q12.3		 likely pathogenic
NM_012179.4(FBXO7):c.122+245G>A single nucleotide variant FBXO7-related disorder [RCV003911381] Chr22:32475369 [GRCh38]
Chr22:32871356 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.41T>G (p.Leu14Arg) single nucleotide variant Inborn genetic diseases [RCV004389090] Chr22:32475043 [GRCh38]
Chr22:32871030 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.664C>G (p.Leu222Val) single nucleotide variant Inborn genetic diseases [RCV004389092] Chr22:32485086 [GRCh38]
Chr22:32881073 [GRCh37]
Chr22:22q12.3		 likely benign
NM_012179.4(FBXO7):c.1289A>G (p.His430Arg) single nucleotide variant Inborn genetic diseases [RCV004389087] Chr22:32498250 [GRCh38]
Chr22:32894237 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.29G>A (p.Arg10Gln) single nucleotide variant Inborn genetic diseases [RCV004389089] Chr22:32475031 [GRCh38]
Chr22:32871018 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1094C>T (p.Ala365Val) single nucleotide variant Inborn genetic diseases [RCV004389085] Chr22:32493231 [GRCh38]
Chr22:32889218 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.19C>G (p.Leu7Val) single nucleotide variant Inborn genetic diseases [RCV004389088] Chr22:32475021 [GRCh38]
Chr22:32871008 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1282C>G (p.Pro428Ala) single nucleotide variant Inborn genetic diseases [RCV004389086] Chr22:32498243 [GRCh38]
Chr22:32894230 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.541C>T (p.His181Tyr) single nucleotide variant Inborn genetic diseases [RCV004618350] Chr22:32484020 [GRCh38]
Chr22:32880007 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.10:g.(?_32894111)_(32894517_?)del deletion Parkinsonian-pyramidal syndrome [RCV004584016] Chr22:32894111..32894517 [GRCh37]
Chr22:22q12.3		 pathogenic
NC_000022.10:g.(?_32891460)_(32894517_?)del deletion Parkinsonian-pyramidal syndrome [RCV004584027] Chr22:32891460..32894517 [GRCh37]
Chr22:22q12.3		 pathogenic
NM_012179.4(FBXO7):c.205G>A (p.Val69Ile) single nucleotide variant not provided [RCV004790873] Chr22:32479063 [GRCh38]
Chr22:32875050 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1204C>A (p.Gln402Lys) single nucleotide variant not provided [RCV004729163] Chr22:32498165 [GRCh38]
Chr22:32894152 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_012179.4(FBXO7):c.1538G>A (p.Arg513Gln) single nucleotide variant not specified [RCV004699912] Chr22:32498499 [GRCh38]
Chr22:32894486 [GRCh37]
Chr22:22q12.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2080
Count of miRNA genes:727
Interacting mature miRNAs:825
Transcripts:ENST00000266087, ENST00000382058, ENST00000397426, ENST00000420700, ENST00000425028, ENST00000444207, ENST00000452138, ENST00000465418, ENST00000484607, ENST00000492535
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
1581529BP71_HBlood pressure QTL 71 (human)20.001Blood pressurepulse pressure221109496637094966Human
406993731GWAS642707_Hmean corpuscular volume QTL GWAS642707 (human)2e-189mean corpuscular volumemean corpuscular volume (CMO:0000038)223248575932485760Human
406953669GWAS602645_Hmean corpuscular volume QTL GWAS602645 (human)0.0000001mean corpuscular volumemean corpuscular volume (CMO:0000038)223248459832484599Human
406991814GWAS640790_Hmean corpuscular hemoglobin concentration QTL GWAS640790 (human)5e-157mean corpuscular hemoglobin concentrationmean corpuscular hemoglobin concentration (CMO:0000291)223248711632487117Human
2289428BW313_HBody weight QTL 313 (human)2.090.0015Body weightBMI221134428437344284Human
406949959GWAS598935_Hmean corpuscular hemoglobin QTL GWAS598935 (human)3e-13mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)223248459832484599Human
407079102GWAS728078_Hobsolete_red blood cell distribution width QTL GWAS728078 (human)2e-49obsolete_red blood cell distribution widthred blood cell distribution width- standard deviation (CMO:0003232)223247714032477141Human
406998668GWAS647644_Hmean corpuscular volume QTL GWAS647644 (human)2e-18mean corpuscular volumemean corpuscular volume (CMO:0000038)223248575932485760Human
406988797GWAS637773_Hmean corpuscular hemoglobin concentration QTL GWAS637773 (human)4e-17mean corpuscular hemoglobin concentrationmean corpuscular hemoglobin concentration (CMO:0000291)223248575932485760Human

Markers in Region
FBXO7_1644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,141 - 32,894,903UniSTSGRCh37
Build 362231,224,141 - 31,224,903RGDNCBI36
Celera2216,696,313 - 16,697,075RGD
HuRef2215,851,323 - 15,852,085UniSTS
ECD00781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,881,396 - 32,882,286UniSTSGRCh37
Build 362231,211,396 - 31,212,286RGDNCBI36
Celera2216,683,569 - 16,684,459RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,838,620 - 15,839,510UniSTS
ECD00809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,870,509 - 32,871,398UniSTSGRCh37
Build 362231,200,509 - 31,201,398RGDNCBI36
Celera2216,672,681 - 16,673,570RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,827,733 - 15,828,622UniSTS
ECD00930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,871,437 - 32,872,321UniSTSGRCh37
Build 362231,201,437 - 31,202,321RGDNCBI36
Celera2216,673,609 - 16,674,493RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,828,661 - 15,829,545UniSTS
ECD01492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,880,501 - 32,881,364UniSTSGRCh37
Build 362231,210,501 - 31,211,364RGDNCBI36
Celera2216,682,674 - 16,683,537RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,837,725 - 15,838,588UniSTS
ECD03561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,877,752 - 32,878,543UniSTSGRCh37
Build 362231,207,752 - 31,208,543RGDNCBI36
Celera2216,679,924 - 16,680,716RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,834,976 - 15,835,767UniSTS
ECD04539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,979 - 32,877,740UniSTSGRCh37
Build 362231,206,979 - 31,207,740RGDNCBI36
Celera2216,679,151 - 16,679,912RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,834,203 - 15,834,964UniSTS
ECD07375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,072 - 32,894,755UniSTSGRCh37
Build 362231,224,072 - 31,224,755RGDNCBI36
Celera2216,696,244 - 16,696,927RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,851,254 - 15,851,937UniSTS
ECD07961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,883,350 - 32,884,017UniSTSGRCh37
Build 362231,213,350 - 31,214,017RGDNCBI36
Celera2216,685,523 - 16,686,190RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,840,574 - 15,841,241UniSTS
ECD09308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,884,158 - 32,884,790UniSTSGRCh37
Build 362231,214,158 - 31,214,790RGDNCBI36
Celera2216,686,331 - 16,686,963RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,841,382 - 15,842,014UniSTS
ECD10459  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,882,701 - 32,883,302UniSTSGRCh37
Build 362231,212,701 - 31,213,302RGDNCBI36
Celera2216,684,874 - 16,685,475RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,839,925 - 15,840,526UniSTS
ECD10686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,626 - 32,891,220UniSTSGRCh37
Build 362231,220,626 - 31,221,220RGDNCBI36
Celera2216,692,798 - 16,693,392RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,849 - 15,848,443UniSTS
ECD10988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,891,226 - 32,891,811UniSTSGRCh37
Build 362231,221,226 - 31,221,811RGDNCBI36
Celera2216,693,398 - 16,693,983RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,848,449 - 15,849,034UniSTS
ECD11459  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,885,607 - 32,886,178UniSTSGRCh37
Build 362231,215,607 - 31,216,178RGDNCBI36
Celera2216,687,780 - 16,688,351RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,842,831 - 15,843,402UniSTS
ECD12310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,888,784 - 32,889,331UniSTSGRCh37
Build 362231,218,784 - 31,219,331RGDNCBI36
Celera2216,690,957 - 16,691,504RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,846,008 - 15,846,555UniSTS
ECD12843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,886,825 - 32,887,358UniSTSGRCh37
Build 362231,216,825 - 31,217,358RGDNCBI36
Celera2216,688,998 - 16,689,531RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,844,049 - 15,844,582UniSTS
ECD13058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,879,762 - 32,880,289UniSTSGRCh37
Build 362231,209,762 - 31,210,289RGDNCBI36
Celera2216,681,935 - 16,682,462RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,836,986 - 15,837,513UniSTS
ECD14904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,873,315 - 32,873,798UniSTSGRCh37
Build 362231,203,315 - 31,203,798RGDNCBI36
Celera2216,675,487 - 16,675,970RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,830,539 - 15,831,022UniSTS
ECD15688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,875,718 - 32,876,182UniSTSGRCh37
Build 362231,205,718 - 31,206,182RGDNCBI36
Celera2216,677,890 - 16,678,354RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,832,942 - 15,833,406UniSTS
ECD16274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,874,898 - 32,875,345UniSTSGRCh37
Build 362231,204,898 - 31,205,345RGDNCBI36
Celera2216,677,070 - 16,677,517RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,832,122 - 15,832,569UniSTS
ECD16676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,878,920 - 32,879,350UniSTSGRCh37
Build 362231,208,920 - 31,209,350RGDNCBI36
Celera2216,681,093 - 16,681,523RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,836,144 - 15,836,574UniSTS
ECD16823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,407 - 32,889,831UniSTSGRCh37
Build 362231,219,407 - 31,219,831RGDNCBI36
Celera2216,691,580 - 16,692,004RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,846,631 - 15,847,055UniSTS
ECD17334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,872,809 - 32,873,212UniSTSGRCh37
Build 362231,202,809 - 31,203,212RGDNCBI36
Celera2216,674,981 - 16,675,384RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,830,033 - 15,830,436UniSTS
ECD18298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,888,108 - 32,888,473UniSTSGRCh37
Build 362231,218,108 - 31,218,473RGDNCBI36
Celera2216,690,281 - 16,690,646RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,845,332 - 15,845,697UniSTS
ECD18637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,295 - 32,876,647UniSTSGRCh37
Build 362231,206,295 - 31,206,647RGDNCBI36
Celera2216,678,467 - 16,678,819RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,833,519 - 15,833,871UniSTS
ECD21445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,872,403 - 32,872,652UniSTSGRCh37
Build 362231,202,403 - 31,202,652RGDNCBI36
Celera2216,674,575 - 16,674,824RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,829,627 - 15,829,876UniSTS
ECD23283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,121 - 32,890,314UniSTSGRCh37
Build 362231,220,121 - 31,220,314RGDNCBI36
Celera2216,692,293 - 16,692,486RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,344 - 15,847,537UniSTS
REN78054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,869,093 - 32,869,317UniSTSGRCh37
Build 362231,199,093 - 31,199,317RGDNCBI36
Celera2216,671,265 - 16,671,489RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,826,317 - 15,826,541UniSTS
REN78055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,869,285 - 32,869,558UniSTSGRCh37
Build 362231,199,285 - 31,199,558RGDNCBI36
Celera2216,671,457 - 16,671,730RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,826,509 - 15,826,782UniSTS
REN78056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,869,546 - 32,869,783UniSTSGRCh37
Build 362231,199,546 - 31,199,783RGDNCBI36
Celera2216,671,718 - 16,671,955RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,826,770 - 15,827,007UniSTS
REN78057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,869,763 - 32,870,028UniSTSGRCh37
Build 362231,199,763 - 31,200,028RGDNCBI36
Celera2216,671,935 - 16,672,200RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,826,987 - 15,827,252UniSTS
REN78058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,869,952 - 32,870,205UniSTSGRCh37
Build 362231,199,952 - 31,200,205RGDNCBI36
Celera2216,672,124 - 16,672,377RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,827,176 - 15,827,429UniSTS
REN78059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,870,509 - 32,870,733UniSTSGRCh37
Build 362231,200,509 - 31,200,733RGDNCBI36
Celera2216,672,681 - 16,672,905RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,827,733 - 15,827,957UniSTS
REN78060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,870,569 - 32,870,820UniSTSGRCh37
Build 362231,200,569 - 31,200,820RGDNCBI36
Celera2216,672,741 - 16,672,992RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,827,793 - 15,828,044UniSTS
REN78061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,870,859 - 32,871,095UniSTSGRCh37
Build 362231,200,859 - 31,201,095RGDNCBI36
Celera2216,673,031 - 16,673,267RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,828,083 - 15,828,319UniSTS
REN78062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,870,865 - 32,871,102UniSTSGRCh37
Build 362231,200,865 - 31,201,102RGDNCBI36
Celera2216,673,037 - 16,673,274RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,828,089 - 15,828,326UniSTS
REN78063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,871,331 - 32,871,555UniSTSGRCh37
Build 362231,201,331 - 31,201,555RGDNCBI36
Celera2216,673,503 - 16,673,727RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,828,555 - 15,828,779UniSTS
REN78064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,871,522 - 32,871,776UniSTSGRCh37
Build 362231,201,522 - 31,201,776RGDNCBI36
Celera2216,673,694 - 16,673,948RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,828,746 - 15,829,000UniSTS
REN78065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,871,753 - 32,872,006UniSTSGRCh37
Build 362231,201,753 - 31,202,006RGDNCBI36
Celera2216,673,925 - 16,674,178RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,828,977 - 15,829,230UniSTS
REN78066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,871,982 - 32,872,231UniSTSGRCh37
Build 362231,201,982 - 31,202,231RGDNCBI36
Celera2216,674,154 - 16,674,403RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,829,206 - 15,829,455UniSTS
REN78067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,872,226 - 32,872,462UniSTSGRCh37
Build 362231,202,226 - 31,202,462RGDNCBI36
Celera2216,674,398 - 16,674,634RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,829,450 - 15,829,686UniSTS
REN78068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,872,406 - 32,872,651UniSTSGRCh37
Build 362231,202,406 - 31,202,651RGDNCBI36
Celera2216,674,578 - 16,674,823RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,829,630 - 15,829,875UniSTS
REN78069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,872,636 - 32,872,906UniSTSGRCh37
Build 362231,202,636 - 31,202,906RGDNCBI36
Celera2216,674,808 - 16,675,078RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,829,860 - 15,830,130UniSTS
REN78070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,872,887 - 32,873,136UniSTSGRCh37
Build 362231,202,887 - 31,203,136RGDNCBI36
Celera2216,675,059 - 16,675,308RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,830,111 - 15,830,360UniSTS
REN78071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,873,130 - 32,873,376UniSTSGRCh37
Build 362231,203,130 - 31,203,376RGDNCBI36
Celera2216,675,302 - 16,675,548RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,830,354 - 15,830,600UniSTS
REN78072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,873,350 - 32,873,577UniSTSGRCh37
Build 362231,203,350 - 31,203,577RGDNCBI36
Celera2216,675,522 - 16,675,749RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,830,574 - 15,830,801UniSTS
REN78073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,873,573 - 32,873,803UniSTSGRCh37
Build 362231,203,573 - 31,203,803RGDNCBI36
Celera2216,675,745 - 16,675,975RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,830,797 - 15,831,027UniSTS
REN78074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,873,786 - 32,874,034UniSTSGRCh37
Build 362231,203,786 - 31,204,034RGDNCBI36
Celera2216,675,958 - 16,676,206RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,831,010 - 15,831,258UniSTS
REN78075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,874,028 - 32,874,274UniSTSGRCh37
Build 362231,204,028 - 31,204,274RGDNCBI36
Celera2216,676,200 - 16,676,446RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,831,252 - 15,831,498UniSTS
REN78076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,874,234 - 32,874,502UniSTSGRCh37
Build 362231,204,234 - 31,204,502RGDNCBI36
Celera2216,676,406 - 16,676,674RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,831,458 - 15,831,726UniSTS
REN78077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,874,357 - 32,874,596UniSTSGRCh37
Build 362231,204,357 - 31,204,596RGDNCBI36
Celera2216,676,529 - 16,676,768RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,831,581 - 15,831,820UniSTS
REN78078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,874,511 - 32,874,758UniSTSGRCh37
Build 362231,204,511 - 31,204,758RGDNCBI36
Celera2216,676,683 - 16,676,930RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,831,735 - 15,831,982UniSTS
REN78079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,874,736 - 32,874,983UniSTSGRCh37
Build 362231,204,736 - 31,204,983RGDNCBI36
Celera2216,676,908 - 16,677,155RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,831,960 - 15,832,207UniSTS
REN78080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,874,960 - 32,875,221UniSTSGRCh37
Build 362231,204,960 - 31,205,221RGDNCBI36
Celera2216,677,132 - 16,677,393RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,832,184 - 15,832,445UniSTS
REN78081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,875,126 - 32,875,350UniSTSGRCh37
Build 362231,205,126 - 31,205,350RGDNCBI36
Celera2216,677,298 - 16,677,522RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,832,350 - 15,832,574UniSTS
REN78082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,875,673 - 32,875,925UniSTSGRCh37
Build 362231,205,673 - 31,205,925RGDNCBI36
Celera2216,677,845 - 16,678,097RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,832,897 - 15,833,149UniSTS
REN78083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,875,902 - 32,876,152UniSTSGRCh37
Build 362231,205,902 - 31,206,152RGDNCBI36
Celera2216,678,074 - 16,678,324RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,833,126 - 15,833,376UniSTS
REN78084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,134 - 32,876,384UniSTSGRCh37
Build 362231,206,134 - 31,206,384RGDNCBI36
Celera2216,678,306 - 16,678,556RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,833,358 - 15,833,608UniSTS
REN78085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,360 - 32,876,593UniSTSGRCh37
Build 362231,206,360 - 31,206,593RGDNCBI36
Celera2216,678,532 - 16,678,765RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,833,584 - 15,833,817UniSTS
REN78086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,515 - 32,876,748UniSTSGRCh37
Build 362231,206,515 - 31,206,748RGDNCBI36
Celera2216,678,687 - 16,678,920RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,833,739 - 15,833,972UniSTS
REN78087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,740 - 32,877,002UniSTSGRCh37
Build 362231,206,740 - 31,207,002RGDNCBI36
Celera2216,678,912 - 16,679,174RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,833,964 - 15,834,226UniSTS
REN78088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,979 - 32,877,245UniSTSGRCh37
Build 362231,206,979 - 31,207,245RGDNCBI36
Celera2216,679,151 - 16,679,417RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,834,203 - 15,834,469UniSTS
REN78089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,877,223 - 32,877,469UniSTSGRCh37
Build 362231,207,223 - 31,207,469RGDNCBI36
Celera2216,679,395 - 16,679,641RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,834,447 - 15,834,693UniSTS
REN78090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,877,445 - 32,877,669UniSTSGRCh37
Build 362231,207,445 - 31,207,669RGDNCBI36
Celera2216,679,617 - 16,679,841RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,834,669 - 15,834,893UniSTS
REN78091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,877,641 - 32,877,868UniSTSGRCh37
Build 362231,207,641 - 31,207,868RGDNCBI36
Celera2216,679,813 - 16,680,040RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,834,865 - 15,835,092UniSTS
REN78092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,877,843 - 32,878,104UniSTSGRCh37
Build 362231,207,843 - 31,208,104RGDNCBI36
Celera2216,680,015 - 16,680,277RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,835,067 - 15,835,328UniSTS
REN78093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,878,082 - 32,878,325UniSTSGRCh37
Build 362231,208,082 - 31,208,325RGDNCBI36
Celera2216,680,255 - 16,680,498RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,835,306 - 15,835,549UniSTS
REN78094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,878,293 - 32,878,548UniSTSGRCh37
Build 362231,208,293 - 31,208,548RGDNCBI36
Celera2216,680,466 - 16,680,721RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,835,517 - 15,835,772UniSTS
REN78095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,878,538 - 32,878,769UniSTSGRCh37
Build 362231,208,538 - 31,208,769RGDNCBI36
Celera2216,680,711 - 16,680,942RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,835,762 - 15,835,993UniSTS
REN78096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,878,745 - 32,878,998UniSTSGRCh37
Build 362231,208,745 - 31,208,998RGDNCBI36
Celera2216,680,918 - 16,681,171RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,835,969 - 15,836,222UniSTS
REN78097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,878,975 - 32,879,231UniSTSGRCh37
Build 362231,208,975 - 31,209,231RGDNCBI36
Celera2216,681,148 - 16,681,404RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,836,199 - 15,836,455UniSTS
REN78098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,879,166 - 32,879,409UniSTSGRCh37
Build 362231,209,166 - 31,209,409RGDNCBI36
Celera2216,681,339 - 16,681,582RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,836,390 - 15,836,633UniSTS
REN78099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,879,388 - 32,879,641UniSTSGRCh37
Build 362231,209,388 - 31,209,641RGDNCBI36
Celera2216,681,561 - 16,681,814RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,836,612 - 15,836,865UniSTS
REN78100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,879,626 - 32,879,875UniSTSGRCh37
Build 362231,209,626 - 31,209,875RGDNCBI36
Celera2216,681,799 - 16,682,048RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,836,850 - 15,837,099UniSTS
REN78101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,879,769 - 32,880,021UniSTSGRCh37
Build 362231,209,769 - 31,210,021RGDNCBI36
Celera2216,681,942 - 16,682,194RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,836,993 - 15,837,245UniSTS
REN78102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,880,002 - 32,880,253UniSTSGRCh37
Build 362231,210,002 - 31,210,253RGDNCBI36
Celera2216,682,175 - 16,682,426RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,837,226 - 15,837,477UniSTS
REN78103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,880,238 - 32,880,488UniSTSGRCh37
Build 362231,210,238 - 31,210,488RGDNCBI36
Celera2216,682,411 - 16,682,661RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,837,462 - 15,837,712UniSTS
REN78104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,880,465 - 32,880,697UniSTSGRCh37
Build 362231,210,465 - 31,210,697RGDNCBI36
Celera2216,682,638 - 16,682,870RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,837,689 - 15,837,921UniSTS
REN78105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,880,592 - 32,880,829UniSTSGRCh37
Build 362231,210,592 - 31,210,829RGDNCBI36
Celera2216,682,765 - 16,683,002RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,837,816 - 15,838,053UniSTS
REN78106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,880,804 - 32,881,049UniSTSGRCh37
Build 362231,210,804 - 31,211,049RGDNCBI36
Celera2216,682,977 - 16,683,222RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,838,028 - 15,838,273UniSTS
REN78107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,881,026 - 32,881,283UniSTSGRCh37
Build 362231,211,026 - 31,211,283RGDNCBI36
Celera2216,683,199 - 16,683,456RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,838,250 - 15,838,507UniSTS
REN78108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,881,250 - 32,881,516UniSTSGRCh37
Build 362231,211,250 - 31,211,516RGDNCBI36
Celera2216,683,423 - 16,683,689RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,838,474 - 15,838,740UniSTS
REN78109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,881,513 - 32,881,751UniSTSGRCh37
Build 362231,211,513 - 31,211,751RGDNCBI36
Celera2216,683,686 - 16,683,924RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,838,737 - 15,838,975UniSTS
REN78110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,881,724 - 32,881,978UniSTSGRCh37
Build 362231,211,724 - 31,211,978RGDNCBI36
Celera2216,683,897 - 16,684,151RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,838,948 - 15,839,202UniSTS
REN78111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,881,976 - 32,882,212UniSTSGRCh37
Build 362231,211,976 - 31,212,212RGDNCBI36
Celera2216,684,149 - 16,684,385RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,839,200 - 15,839,436UniSTS
REN78112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,882,156 - 32,882,415UniSTSGRCh37
Build 362231,212,156 - 31,212,415RGDNCBI36
Celera2216,684,329 - 16,684,588RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,839,380 - 15,839,639UniSTS
REN78113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,882,375 - 32,882,626UniSTSGRCh37
Build 362231,212,375 - 31,212,626RGDNCBI36
Celera2216,684,548 - 16,684,799RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,839,599 - 15,839,850UniSTS
REN78114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,882,611 - 32,882,858UniSTSGRCh37
Build 362231,212,611 - 31,212,858RGDNCBI36
Celera2216,684,784 - 16,685,031RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,839,835 - 15,840,082UniSTS
REN78115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,882,853 - 32,883,077UniSTSGRCh37
Build 362231,212,853 - 31,213,077RGDNCBI36
Celera2216,685,026 - 16,685,250RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,840,077 - 15,840,301UniSTS
REN78116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,883,069 - 32,883,318UniSTSGRCh37
Build 362231,213,069 - 31,213,318RGDNCBI36
Celera2216,685,242 - 16,685,491RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,840,293 - 15,840,542UniSTS
REN78117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,883,295 - 32,883,561UniSTSGRCh37
Build 362231,213,295 - 31,213,561RGDNCBI36
Celera2216,685,468 - 16,685,734RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,840,519 - 15,840,785UniSTS
REN78118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,883,540 - 32,883,781UniSTSGRCh37
Build 362231,213,540 - 31,213,781RGDNCBI36
Celera2216,685,713 - 16,685,954RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,840,764 - 15,841,005UniSTS
REN78119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,883,768 - 32,884,017UniSTSGRCh37
Build 362231,213,768 - 31,214,017RGDNCBI36
Celera2216,685,941 - 16,686,190RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,840,992 - 15,841,241UniSTS
REN78120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,883,994 - 32,884,228UniSTSGRCh37
Build 362231,213,994 - 31,214,228RGDNCBI36
Celera2216,686,167 - 16,686,401RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,841,218 - 15,841,452UniSTS
REN78121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,884,208 - 32,884,464UniSTSGRCh37
Build 362231,214,208 - 31,214,464RGDNCBI36
Celera2216,686,381 - 16,686,637RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,841,432 - 15,841,688UniSTS
REN78122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,884,441 - 32,884,686UniSTSGRCh37
Build 362231,214,441 - 31,214,686RGDNCBI36
Celera2216,686,614 - 16,686,859RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,841,665 - 15,841,910UniSTS
REN78123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,884,547 - 32,884,791UniSTSGRCh37
Build 362231,214,547 - 31,214,791RGDNCBI36
Celera2216,686,720 - 16,686,964RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,841,771 - 15,842,015UniSTS
REN78124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,884,720 - 32,884,945UniSTSGRCh37
Build 362231,214,720 - 31,214,945RGDNCBI36
Celera2216,686,893 - 16,687,118RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,841,944 - 15,842,169UniSTS
REN78125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,885,114 - 32,885,338UniSTSGRCh37
Build 362231,215,114 - 31,215,338RGDNCBI36
Celera2216,687,287 - 16,687,511RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,842,338 - 15,842,562UniSTS
REN78126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,885,315 - 32,885,562UniSTSGRCh37
Build 362231,215,315 - 31,215,562RGDNCBI36
Celera2216,687,488 - 16,687,735RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,842,539 - 15,842,786UniSTS
REN78127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,885,547 - 32,885,798UniSTSGRCh37
Build 362231,215,547 - 31,215,798RGDNCBI36
Celera2216,687,720 - 16,687,971RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,842,771 - 15,843,022UniSTS
REN78128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,885,775 - 32,886,023UniSTSGRCh37
Build 362231,215,775 - 31,216,023RGDNCBI36
Celera2216,687,948 - 16,688,196RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,842,999 - 15,843,247UniSTS
REN78129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,885,999 - 32,886,232UniSTSGRCh37
Build 362231,215,999 - 31,216,232RGDNCBI36
Celera2216,688,172 - 16,688,405RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,843,223 - 15,843,456UniSTS
REN78130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,886,209 - 32,886,461UniSTSGRCh37
Build 362231,216,209 - 31,216,461RGDNCBI36
Celera2216,688,382 - 16,688,634RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,843,433 - 15,843,685UniSTS
REN78131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,886,438 - 32,886,674UniSTSGRCh37
Build 362231,216,438 - 31,216,674RGDNCBI36
Celera2216,688,611 - 16,688,847RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,843,662 - 15,843,898UniSTS
REN78132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,886,671 - 32,886,923UniSTSGRCh37
Build 362231,216,671 - 31,216,923RGDNCBI36
Celera2216,688,844 - 16,689,096RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,843,895 - 15,844,147UniSTS
REN78133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,886,916 - 32,887,162UniSTSGRCh37
Build 362231,216,916 - 31,217,162RGDNCBI36
Celera2216,689,089 - 16,689,335RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,844,140 - 15,844,386UniSTS
REN78134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,887,159 - 32,887,426UniSTSGRCh37
Build 362231,217,159 - 31,217,426RGDNCBI36
Celera2216,689,332 - 16,689,599RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,844,383 - 15,844,650UniSTS
REN78135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,887,414 - 32,887,679UniSTSGRCh37
Build 362231,217,414 - 31,217,679RGDNCBI36
Celera2216,689,587 - 16,689,852RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,844,638 - 15,844,903UniSTS
REN78136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,887,656 - 32,887,901UniSTSGRCh37
Build 362231,217,656 - 31,217,901RGDNCBI36
Celera2216,689,829 - 16,690,074RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,844,880 - 15,845,125UniSTS
REN78137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,887,880 - 32,888,131UniSTSGRCh37
Build 362231,217,880 - 31,218,131RGDNCBI36
Celera2216,690,053 - 16,690,304RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,845,104 - 15,845,355UniSTS
REN78138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,888,128 - 32,888,386UniSTSGRCh37
Build 362231,218,128 - 31,218,386RGDNCBI36
Celera2216,690,301 - 16,690,559RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,845,352 - 15,845,610UniSTS
REN78139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,888,359 - 32,888,583UniSTSGRCh37
Build 362231,218,359 - 31,218,583RGDNCBI36
Celera2216,690,532 - 16,690,756RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,845,583 - 15,845,807UniSTS
REN78140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,888,579 - 32,888,806UniSTSGRCh37
Build 362231,218,579 - 31,218,806RGDNCBI36
Celera2216,690,752 - 16,690,979RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,845,803 - 15,846,030UniSTS
REN78141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,888,797 - 32,889,044UniSTSGRCh37
Build 362231,218,797 - 31,219,044RGDNCBI36
Celera2216,690,970 - 16,691,217RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,846,021 - 15,846,268UniSTS
REN78142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,028 - 32,889,282UniSTSGRCh37
Build 362231,219,028 - 31,219,282RGDNCBI36
Celera2216,691,201 - 16,691,455RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,846,252 - 15,846,506UniSTS
REN78143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,260 - 32,889,524UniSTSGRCh37
Build 362231,219,260 - 31,219,524RGDNCBI36
Celera2216,691,433 - 16,691,697RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,846,484 - 15,846,748UniSTS
REN78144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,500 - 32,889,734UniSTSGRCh37
Build 362231,219,500 - 31,219,734RGDNCBI36
Celera2216,691,673 - 16,691,907RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,846,724 - 15,846,958UniSTS
REN78145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,605 - 32,889,829UniSTSGRCh37
Build 362231,219,605 - 31,219,829RGDNCBI36
Celera2216,691,778 - 16,692,002RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,846,829 - 15,847,053UniSTS
REN78146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,797 - 32,890,046UniSTSGRCh37
Build 362231,219,797 - 31,220,046RGDNCBI36
Celera2216,691,970 - 16,692,219RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,021 - 15,847,270UniSTS
REN78147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,034 - 32,890,271UniSTSGRCh37
Build 362231,220,034 - 31,220,271RGDNCBI36
Celera2216,692,207 - 16,692,443RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,258 - 15,847,494UniSTS
REN78148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,239 - 32,890,477UniSTSGRCh37
Build 362231,220,239 - 31,220,477RGDNCBI36
Celera2216,692,411 - 16,692,649RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,462 - 15,847,700UniSTS
REN78149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,444 - 32,890,690UniSTSGRCh37
Build 362231,220,444 - 31,220,690RGDNCBI36
Celera2216,692,616 - 16,692,862RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,667 - 15,847,913UniSTS
REN78150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,666 - 32,890,915UniSTSGRCh37
Build 362231,220,666 - 31,220,915RGDNCBI36
Celera2216,692,838 - 16,693,087RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,889 - 15,848,138UniSTS
REN78151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,895 - 32,891,142UniSTSGRCh37
Build 362231,220,895 - 31,221,142RGDNCBI36
Celera2216,693,067 - 16,693,314RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,848,118 - 15,848,365UniSTS
REN78152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,891,084 - 32,891,308UniSTSGRCh37
Build 362231,221,084 - 31,221,308RGDNCBI36
Celera2216,693,256 - 16,693,480RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,848,307 - 15,848,531UniSTS
REN78153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,891,246 - 32,891,512UniSTSGRCh37
Build 362231,221,246 - 31,221,512RGDNCBI36
Celera2216,693,418 - 16,693,684RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,848,469 - 15,848,735UniSTS
REN78154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,891,424 - 32,891,687UniSTSGRCh37
Build 362231,221,424 - 31,221,687RGDNCBI36
Celera2216,693,596 - 16,693,859RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,848,647 - 15,848,910UniSTS
REN78155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,891,657 - 32,891,928UniSTSGRCh37
Build 362231,221,657 - 31,221,928RGDNCBI36
Celera2216,693,829 - 16,694,100RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,848,880 - 15,849,151UniSTS
REN78156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,891,914 - 32,892,154UniSTSGRCh37
Build 362231,221,914 - 31,222,154RGDNCBI36
Celera2216,694,086 - 16,694,326RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,849,137 - 15,849,377UniSTS
REN78157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,891,959 - 32,892,190UniSTSGRCh37
Build 362231,221,959 - 31,222,190RGDNCBI36
Celera2216,694,131 - 16,694,362RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,849,182 - 15,849,413UniSTS
REN78158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,892,502 - 32,892,726UniSTSGRCh37
Build 362231,222,502 - 31,222,726RGDNCBI36
Celera2216,694,674 - 16,694,898RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,849,725 - 15,849,949UniSTS
REN78159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,892,706 - 32,892,959UniSTSGRCh37
Build 362231,222,706 - 31,222,959RGDNCBI36
Celera2216,694,878 - 16,695,131RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,849,929 - 15,850,182UniSTS
REN78160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,892,872 - 32,893,115UniSTSGRCh37
Build 362231,222,872 - 31,223,115RGDNCBI36
Celera2216,695,044 - 16,695,287RGD
Cytogenetic Map22q12-q13UniSTS
REN78161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,893,067 - 32,893,293UniSTSGRCh37
Build 362231,223,067 - 31,223,293RGDNCBI36
Celera2216,695,239 - 16,695,465RGD
Cytogenetic Map22q12-q13UniSTS
REN78162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,893,269 - 32,893,534UniSTSGRCh37
Build 362231,223,269 - 31,223,534RGDNCBI36
Celera2216,695,441 - 16,695,706RGD
Cytogenetic Map22q12-q13UniSTS
REN78163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,893,531 - 32,893,773UniSTSGRCh37
Build 362231,223,531 - 31,223,773RGDNCBI36
Celera2216,695,703 - 16,695,945RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,850,713 - 15,850,955UniSTS
REN78164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,893,748 - 32,894,000UniSTSGRCh37
Build 362231,223,748 - 31,224,000RGDNCBI36
Celera2216,695,920 - 16,696,172RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,850,930 - 15,851,182UniSTS
REN78165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,893,977 - 32,894,226UniSTSGRCh37
Build 362231,223,977 - 31,224,226RGDNCBI36
Celera2216,696,149 - 16,696,398RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,851,159 - 15,851,408UniSTS
REN78166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,200 - 32,894,431UniSTSGRCh37
Build 362231,224,200 - 31,224,431RGDNCBI36
Celera2216,696,372 - 16,696,603RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,851,382 - 15,851,613UniSTS
REN78167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,409 - 32,894,655UniSTSGRCh37
Build 362231,224,409 - 31,224,655RGDNCBI36
Celera2216,696,581 - 16,696,827RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,851,591 - 15,851,837UniSTS
REN78168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,628 - 32,894,888UniSTSGRCh37
Build 362231,224,628 - 31,224,888RGDNCBI36
Celera2216,696,800 - 16,697,060RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,851,810 - 15,852,070UniSTS
REN78169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,874 - 32,895,123UniSTSGRCh37
Build 362231,224,874 - 31,225,123RGDNCBI36
Celera2216,697,046 - 16,697,295RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,852,056 - 15,852,305UniSTS
stSG602804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,869,489 - 32,870,528UniSTSGRCh37
Build 362231,199,489 - 31,200,528RGDNCBI36
Celera2216,671,661 - 16,672,700RGD
HuRef2215,826,713 - 15,827,752UniSTS
stSG602805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,870,509 - 32,871,521UniSTSGRCh37
Build 362231,200,509 - 31,201,521RGDNCBI36
Celera2216,672,681 - 16,673,693RGD
HuRef2215,827,733 - 15,828,745UniSTS
stSG602806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,871,502 - 32,872,828UniSTSGRCh37
Build 362231,201,502 - 31,202,828RGDNCBI36
Celera2216,673,674 - 16,675,000RGD
HuRef2215,828,726 - 15,830,052UniSTS
stSG602807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,872,621 - 32,873,759UniSTSGRCh37
Build 362231,202,621 - 31,203,759RGDNCBI36
Celera2216,674,793 - 16,675,931RGD
HuRef2215,829,845 - 15,830,983UniSTS
stSG602808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,873,740 - 32,875,018UniSTSGRCh37
Build 362231,203,740 - 31,205,018RGDNCBI36
Celera2216,675,912 - 16,677,190RGD
HuRef2215,830,964 - 15,832,242UniSTS
stSG602809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,875,028 - 32,876,518UniSTSGRCh37
Build 362231,205,028 - 31,206,518RGDNCBI36
Celera2216,677,200 - 16,678,690RGD
HuRef2215,832,252 - 15,833,742UniSTS
stSG602810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,876,559 - 32,877,870UniSTSGRCh37
Build 362231,206,559 - 31,207,870RGDNCBI36
Celera2216,678,731 - 16,680,042RGD
HuRef2215,833,783 - 15,835,094UniSTS
stSG602811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,877,855 - 32,879,161UniSTSGRCh37
Build 362231,207,855 - 31,209,161RGDNCBI36
Celera2216,680,027 - 16,681,334RGD
HuRef2215,835,079 - 15,836,385UniSTS
stSG602812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,879,144 - 32,880,185UniSTSGRCh37
Build 362231,209,144 - 31,210,185RGDNCBI36
Celera2216,681,317 - 16,682,358RGD
HuRef2215,836,368 - 15,837,409UniSTS
stSG602813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,880,166 - 32,881,412UniSTSGRCh37
Build 362231,210,166 - 31,211,412RGDNCBI36
Celera2216,682,339 - 16,683,585RGD
HuRef2215,837,390 - 15,838,636UniSTS
stSG602814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,881,393 - 32,882,840UniSTSGRCh37
Build 362231,211,393 - 31,212,840RGDNCBI36
Celera2216,683,566 - 16,685,013RGD
HuRef2215,838,617 - 15,840,064UniSTS
stSG602815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,882,824 - 32,883,030UniSTSGRCh37
Build 362231,212,824 - 31,213,030RGDNCBI36
Celera2216,684,997 - 16,685,203RGD
HuRef2215,840,048 - 15,840,254UniSTS
stSG602816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,883,072 - 32,884,178UniSTSGRCh37
Build 362231,213,072 - 31,214,178RGDNCBI36
Celera2216,685,245 - 16,686,351RGD
HuRef2215,840,296 - 15,841,402UniSTS
stSG602817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,884,158 - 32,885,411UniSTSGRCh37
Build 362231,214,158 - 31,215,411RGDNCBI36
Celera2216,686,331 - 16,687,584RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,841,382 - 15,842,635UniSTS
stSG602818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,885,392 - 32,886,852UniSTSGRCh37
Build 362231,215,392 - 31,216,852RGDNCBI36
Celera2216,687,565 - 16,689,025RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,842,616 - 15,844,076UniSTS
stSG602819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,886,833 - 32,888,317UniSTSGRCh37
Build 362231,216,833 - 31,218,317RGDNCBI36
Celera2216,689,006 - 16,690,490RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,844,057 - 15,845,541UniSTS
stSG602821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,732 - 32,891,111UniSTSGRCh37
Build 362231,219,732 - 31,221,111RGDNCBI36
Celera2216,691,905 - 16,693,283RGD
HuRef2215,846,956 - 15,848,334UniSTS
stSG602822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,890,743 - 32,891,803UniSTSGRCh37
Build 362231,220,743 - 31,221,803RGDNCBI36
Celera2216,692,915 - 16,693,975RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,966 - 15,849,026UniSTS
stSG602823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,071 - 32,895,180UniSTSGRCh37
Build 362231,224,071 - 31,225,180RGDNCBI36
Celera2216,696,243 - 16,697,352RGD
HuRef2215,851,253 - 15,852,362UniSTS
D22S1127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,967 - 32,890,054UniSTSGRCh37
Build 362231,219,967 - 31,220,054RGDNCBI36
Celera2216,692,140 - 16,692,227RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,191 - 15,847,278UniSTS
GeneMap99-GB4 RH Map2298.33UniSTS
A002E09  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,894,650 - 32,894,778UniSTSGRCh37
Build 362231,224,650 - 31,224,778RGDNCBI36
Celera2216,696,822 - 16,696,950RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,851,832 - 15,851,960UniSTS
GeneMap99-GB4 RH Map2292.32UniSTS
Whitehead-RH Map2294.4UniSTS
SHGC-53239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372232,889,865 - 32,890,058UniSTSGRCh37
Build 362231,219,865 - 31,220,058RGDNCBI36
Celera2216,692,038 - 16,692,231RGD
Cytogenetic Map22q12-q13UniSTS
HuRef2215,847,089 - 15,847,282UniSTS
TNG Radiation Hybrid Map226847.0UniSTS
D5S1597E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map6q16.2UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


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
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_016001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001033024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001257990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_012179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF129537 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF233225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK054739 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK226087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297841 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301716 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL021937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL035068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL050254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041004 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI821903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ326686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU584368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX362053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX409547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR456491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OP794565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z71183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000266087   ⟹   ENSP00000266087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,474,811 - 32,498,829 (+)Ensembl
Ensembl Acc Id: ENST00000397426   ⟹   ENSP00000380571
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,475,257 - 32,498,829 (+)Ensembl
Ensembl Acc Id: ENST00000420700   ⟹   ENSP00000406155
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,474,676 - 32,498,829 (+)Ensembl
Ensembl Acc Id: ENST00000425028   ⟹   ENSP00000395823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,474,798 - 32,498,829 (+)Ensembl
Ensembl Acc Id: ENST00000444207   ⟹   ENSP00000404388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,475,593 - 32,483,983 (+)Ensembl
Ensembl Acc Id: ENST00000452138   ⟹   ENSP00000388547
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,475,237 - 32,498,608 (+)Ensembl
Ensembl Acc Id: ENST00000465418
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,478,035 - 32,479,231 (+)Ensembl
Ensembl Acc Id: ENST00000484607
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,487,288 - 32,491,113 (+)Ensembl
Ensembl Acc Id: ENST00000492535
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2232,475,015 - 32,498,829 (+)Ensembl
RefSeq Acc Id: NM_001033024   ⟹   NP_001028196
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,475,268 - 32,498,829 (+)NCBI
GRCh372232,870,707 - 32,894,818 (+)ENTREZGENE
Build 362231,201,224 - 31,224,818 (+)NCBI Archive
HuRef2215,827,931 - 15,852,000 (+)ENTREZGENE
CHM1_12232,830,580 - 32,854,178 (+)NCBI
T2T-CHM13v2.02232,939,162 - 32,962,724 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001257990   ⟹   NP_001244919
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,475,268 - 32,498,829 (+)NCBI
GRCh372232,870,707 - 32,894,818 (+)NCBI
HuRef2215,827,931 - 15,852,000 (+)NCBI
CHM1_12232,830,580 - 32,854,178 (+)NCBI
T2T-CHM13v2.02232,939,162 - 32,962,724 (+)NCBI
Sequence:
RefSeq Acc Id: NM_012179   ⟹   NP_036311
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,474,811 - 32,498,829 (+)NCBI
GRCh372232,870,707 - 32,894,818 (+)ENTREZGENE
Build 362231,200,707 - 31,224,818 (+)NCBI Archive
HuRef2215,827,931 - 15,852,000 (+)ENTREZGENE
CHM1_12232,830,063 - 32,854,178 (+)NCBI
T2T-CHM13v2.02232,938,705 - 32,962,724 (+)NCBI
Sequence:
RefSeq Acc Id: NP_036311   ⟸   NM_012179
- Peptide Label: isoform 1
- UniProtKB: Q9UF21 (UniProtKB/Swiss-Prot),   Q96HM6 (UniProtKB/Swiss-Prot),   Q5TI86 (UniProtKB/Swiss-Prot),   Q5TGC4 (UniProtKB/Swiss-Prot),   B4DWX5 (UniProtKB/Swiss-Prot),   B4DNB3 (UniProtKB/Swiss-Prot),   Q9UKT2 (UniProtKB/Swiss-Prot),   Q9Y3I1 (UniProtKB/Swiss-Prot),   A8K7F7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001028196   ⟸   NM_001033024
- Peptide Label: isoform 2
- UniProtKB: A8K7F7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001244919   ⟸   NM_001257990
- Peptide Label: isoform 3
- UniProtKB: Q9Y3I1 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000266087   ⟸   ENST00000266087
Ensembl Acc Id: ENSP00000395823   ⟸   ENST00000425028
Ensembl Acc Id: ENSP00000388547   ⟸   ENST00000452138
Ensembl Acc Id: ENSP00000404388   ⟸   ENST00000444207
Ensembl Acc Id: ENSP00000406155   ⟸   ENST00000420700
Ensembl Acc Id: ENSP00000380571   ⟸   ENST00000397426
Protein Domains
F-box

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y3I1-F1-model_v2 AlphaFold Q9Y3I1 1-522 view protein structure

Promoters
RGD ID:6799984
Promoter ID:HG_KWN:42492
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_001033024,   OTTHUMT00000129001,   OTTHUMT00000129004,   OTTHUMT00000129005,   OTTHUMT00000129006,   UC003AMP.1,   UC003AMR.1,   UC003AMS.1,   UC003AMU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,200,611 - 31,201,362 (+)MPROMDB
RGD ID:6799985
Promoter ID:HG_KWN:42495
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat
Transcripts:UC003AMV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362231,216,586 - 31,217,086 (+)MPROMDB
RGD ID:13603832
Promoter ID:EPDNEW_H28100
Type:initiation region
Name:FBXO7_1
Description:F-box protein 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28101  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,474,811 - 32,474,871EPDNEW
RGD ID:13603834
Promoter ID:EPDNEW_H28101
Type:multiple initiation site
Name:FBXO7_2
Description:F-box protein 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28100  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382232,487,289 - 32,487,349EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13586 AgrOrtholog
COSMIC FBXO7 COSMIC
Ensembl Genes ENSG00000100225 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000266087 ENTREZGENE
  ENST00000266087.12 UniProtKB/Swiss-Prot
  ENST00000397426 ENTREZGENE
  ENST00000397426.5 UniProtKB/Swiss-Prot
  ENST00000420700.5 UniProtKB/TrEMBL
  ENST00000425028.5 UniProtKB/TrEMBL
  ENST00000444207.1 UniProtKB/TrEMBL
  ENST00000452138 ENTREZGENE
  ENST00000452138.3 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.1280.50 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.1000.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000100225 GTEx
HGNC ID HGNC:13586 ENTREZGENE
Human Proteome Map FBXO7 Human Proteome Map
InterPro F-box-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  F-box_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Fbxo7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PI31_Prot_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ubiquitin-like_domsf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:25793 UniProtKB/Swiss-Prot
NCBI Gene 25793 ENTREZGENE
OMIM 605648 OMIM
PANTHER F-BOX ONLY PROTEIN 7 UniProtKB/Swiss-Prot
  F-BOX ONLY PROTEIN 7 UniProtKB/Swiss-Prot
  F-BOX ONLY PROTEIN 7 UniProtKB/TrEMBL
  F-BOX ONLY PROTEIN 7 UniProtKB/TrEMBL
Pfam F-box-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PI31_Prot_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA28047 PharmGKB
PROSITE FBOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART FBOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP F-box domain UniProtKB/TrEMBL
  SSF54236 UniProtKB/Swiss-Prot
  SSF81383 UniProtKB/Swiss-Prot
  Ubiquitin-like UniProtKB/TrEMBL
UniProt A2A282_HUMAN UniProtKB/TrEMBL
  A8K7F7 ENTREZGENE, UniProtKB/TrEMBL
  B4DNB3 ENTREZGENE
  B4DWX5 ENTREZGENE
  F8WBR0_HUMAN UniProtKB/TrEMBL
  F8WDR9_HUMAN UniProtKB/TrEMBL
  FBX7_HUMAN UniProtKB/Swiss-Prot
  Q5TGC4 ENTREZGENE
  Q5TI86 ENTREZGENE
  Q96HM6 ENTREZGENE
  Q9UF21 ENTREZGENE
  Q9UKT2 ENTREZGENE
  Q9Y3I1 ENTREZGENE
UniProt Secondary B4DNB3 UniProtKB/Swiss-Prot
  B4DWX5 UniProtKB/Swiss-Prot
  Q5TGC4 UniProtKB/Swiss-Prot
  Q5TI86 UniProtKB/Swiss-Prot
  Q96HM6 UniProtKB/Swiss-Prot
  Q9UF21 UniProtKB/Swiss-Prot
  Q9UKT2 UniProtKB/Swiss-Prot