RGD:407517379 Rat Genome Database

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Variant: RGD:407517379 -  Homo sapiens

RGD ID: 407517379
ClinVar ID: CV3469966
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: P2RY1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 152,553,575
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_635t1:c.4A>G
NM_002563.5:c.4A>G
LRG_635:g.5840A>G
NG_032896.2:g.5840A>G
More...
03/20/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004650625 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene P2RY1 CLINVAR
OMIM 601167 CLINVAR