RGD:11590286 Rat Genome Database

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Variant: RGD:11590286 -  Homo sapiens

RGD ID: 11590286
ClinVar ID: CV288195
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP31  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 119,136,422
GRCh38 3 119,417,575
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_020754.4:c.*1311A>T
NG_007665.2:g.128203A>T
NC_000003.12:g.119417575A>T
NC_000003.11:g.119136422A>T
More... 		06/14/2016 3 prime utr variant likely benign

Variant Details
Variant Transcripts
Gene Symbol:ARHGAP31
Accession:XM_006713714
Location:3UTRS;EXON

Gene Symbol:ARHGAP31
Accession:NM_020754
Location:3UTRS;EXON

Variant Samples