RGD:150513517 Rat Genome Database

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Variant: RGD:150513517 -  Homo sapiens

RGD ID: 150513517
RS ID: rs138654906
ClinVar ID: CV1211957
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB3GAP2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 220,375,376
GRCh38 1 220,202,034
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.811+242C>T
NG_015837.2:g.75468C>T
NC_000001.11:g.220202034G>A
NC_000001.10:g.220375376G>A
 08/13/2019 intron variant 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 RCV001598478 CLINVAR
dbSNP (RS) rs138654906 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RAB3GAP2 CLINVAR
OMIM 609275 CLINVAR