RGD:14737977 Rat Genome Database

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Variant: RGD:14737977 -  Homo sapiens

RGD ID: 14737977
RS ID: rs150113730
ClinVar ID: CV665179
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRKG1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 53,564,129
GRCh38 10 51,804,369
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001098512.3:c.548-216C>T
NM_006258.4:c.593-216C>T
NG_029982.1:g.818219C>T
NC_000010.11:g.51804369C>T
More... 		06/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRKG1
Accession:NM_001374781
Location:INTRON

Gene Symbol:PRKG1
Accession:XM_011539952
Location:INTRON

Gene Symbol:PRKG1
Accession:XM_017016413
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_001098512
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_006258
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_001374782
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000839167 CLINVAR
dbSNP (RS) rs150113730 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRKG1 CLINVAR
OMIM 176894 CLINVAR