RGD:13626623 Rat Genome Database

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Variant: RGD:13626623 -  Homo sapiens

RGD ID: 13626623
RS ID: rs202058118
ClinVar ID: CV525375
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124902425  PRKG1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 54,011,434
GRCh38 10 52,251,674
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_029982.1:g.1265524A>G
NC_000010.11:g.52251674A>G
NC_000010.10:g.54011434A>G
NM_001098512.3:c.1128+8A>G
More... 		02/15/2018 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


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

Gene Symbol:PRKG1
Accession:NM_006258
Location:INTRON

Gene Symbol:PRKG1
Accession:XM_011539952
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_001374782
Location:INTRON

Gene Symbol:PRKG1
Accession:NM_001098512
Location:INTRON

Gene Symbol:PRKG1
Accession:XM_017016413
Location:INTRON

Gene Symbol:LOC124902425
Accession:XR_007062145
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001412993 CLINVAR
dbSNP (RS) rs202058118 CLINVAR
MedGen C3809513 CLINVAR
NCBI Gene PRKG1 CLINVAR
OMIM 176894 CLINVAR
  615436 CLINVAR