RGD:14734671 Rat Genome Database

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Variant: RGD:14734671 -  Homo sapiens

RGD ID: 14734671
RS ID: rs7097336
ClinVar ID: CV664356
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRKG1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 53,893,888
GRCh38 10 52,134,128
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006258.4:c.1001+223G>A
NM_001098512.3:c.956+223G>A
NG_029982.1:g.1147978G>A
NC_000010.11:g.52134128G>A
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PRKG1
Accession:NM_001374781
Location:5UTRS;INTRON

Gene Symbol:PRKG1
Accession:XM_017016413
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_001374782
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_001098512
Location:INTRON

Gene Symbol:PRKG1
Accession:XM_011539952
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_006258
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000837661 CLINVAR
dbSNP (RS) rs7097336 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PRKG1 CLINVAR
OMIM 176894 CLINVAR