RGD:150479723 Rat Genome Database

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Variant: RGD:150479723 -  Homo sapiens

RGD ID: 150479723
RS ID: rs112968685
ClinVar ID: CV1207883
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB3GAP2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 220,370,016
GRCh38 1 220,196,674
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012414.4:c.812-276A>G
NG_015837.2:g.80828A>G
NC_000001.11:g.220196674T>C
NC_000001.10:g.220370016T>C
 08/12/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RAB3GAP2
Accession:NM_012414
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001590159 CLINVAR
dbSNP (RS) rs112968685 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RAB3GAP2 CLINVAR
OMIM 609275 CLINVAR