rs11098815 Rat Genome Database

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Variant: rs11098815 -  Homo sapiens

RGD ID: 14739472
RS ID: rs11098815
ClinVar ID: CV660175
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FAT4  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 126,402,921
GRCh38 4 125,481,766
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_033865.1:g.170355T>G
NC_000004.12:g.125481766T>G
NC_000004.11:g.126402921T>G
NM_024582.6:c.12816+28T>G
More... 		08/10/2021 intron variant benign AllHighlyPenetrant; none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FAT4
Accession:NM_024582
Location:INTRON

Gene Symbol:FAT4
Accession:NM_001291303
Location:INTRON

Gene Symbol:FAT4
Accession:XM_047416153
Location:INTRON

Gene Symbol:FAT4
Accession:NM_001291285
Location:INTRON

Gene Symbol:FAT4
Accession:XM_047416151
Location:INTRON

Gene Symbol:FAT4
Accession:XM_011532237
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000839890 CLINVAR
  RCV001702733 CLINVAR
  RCV001703240 CLINVAR
  RCV003489933 CLINVAR
dbSNP (RS) rs11098815 CLINVAR
MedGen C3661900 CLINVAR
  C3809875 CLINVAR
  C4014939 CLINVAR
  CN169374 CLINVAR
NCBI Gene FAT4 CLINVAR
OMIM 612411 CLINVAR
  615546 CLINVAR
  616006 CLINVAR