RGD:11593755 Rat Genome Database

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Variant: RGD:11593755 -  Homo sapiens

RGD ID: 11593755
RS ID: rs116944967
ClinVar ID: CV288933
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP31  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 119,135,577
GRCh38 3 119,416,730
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.127358C>T
NC_000003.12:g.119416730C>T
NC_000003.11:g.119135577C>T
NM_020754.2:c.*466C>T
More... 		06/14/2016 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000352060 CLINVAR
dbSNP (RS) rs116944967 CLINVAR
MedGen C0265268 CLINVAR
NCBI Gene ARHGAP31 CLINVAR
OMIM 100300 CLINVAR
  610911 CLINVAR
SNOMED CT 34748004 CLINVAR