RGD:11597741 Rat Genome Database

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Variant: RGD:11597741 -  Homo sapiens

RGD ID: 11597741
ClinVar ID: CV292019
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP31  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 119,137,162
GRCh38 3 119,418,315
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.128943C>A
NC_000003.12:g.119418315C>A
NC_000003.11:g.119137162C>A
NM_020754.2:c.*2051C>A
More...
06/14/2016 3 prime utr variant likely benign

Variant Details
Variant Transcripts
Gene Symbol:ARHGAP31
Accession:NM_020754
Location:3UTRS;EXON

Gene Symbol:ARHGAP31
Accession:XM_006713714
Location:3UTRS;EXON

Variant Samples