RGD:11637171 Rat Genome Database

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Variant: RGD:11637171 -  Homo sapiens

RGD ID: 11637171
RS ID: rs756581922
ClinVar ID: CV267813
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP31  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 119,087,362
GRCh38 3 119,368,515
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007665.2:g.79143C>T
NC_000003.12:g.119368515C>T
NC_000003.11:g.119087362C>T
NP_065805.2:p.Thr116Met
More... 		10/09/2015 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:ARHGAP31
Accession:NM_020754
Location:EXON

Gene Symbol:ARHGAP31
Accession:XM_006713714
Location:EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000281382 CLINVAR
dbSNP (RS) rs756581922 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene ARHGAP31 CLINVAR
OMIM 610911 CLINVAR