RGD:150407874 Rat Genome Database

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Variant: RGD:150407874 -  Homo sapiens

RGD ID: 150407874
RS ID: rs116370890
ClinVar ID: CV1192794
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB3GAP2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 220,369,893
GRCh38 1 220,196,551
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.10:g.220369893G>T
NM_012414.4:c.812-153C>A
NC_000001.11:g.220196551G>T
NG_015837.2:g.80951C>A
 10/17/2018 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 RCV001572465 CLINVAR
dbSNP (RS) rs116370890 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RAB3GAP2 CLINVAR
OMIM 609275 CLINVAR