RGD:11650099 Rat Genome Database

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Variant: RGD:11650099 -  Homo sapiens

RGD ID: 11650099
ClinVar ID: CV288953
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP31  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 119,136,759
GRCh38 3 119,417,912
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.128540C>T
NC_000003.12:g.119417912C>T
NC_000003.11:g.119136759C>T
NM_020754.2:c.*1648C>T
More... 		06/14/2016 3 prime utr variant uncertain significance

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

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

Variant Samples