RGD:150465290 Rat Genome Database

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Variant: RGD:150465290 -  Homo sapiens

RGD ID: 150465290
RS ID: rs144719866
ClinVar ID: CV1201052
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PINK1  PINK1-AS  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 20,975,278
GRCh38 1 20,648,785
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032409.3:c.1251+153C>T
NG_008164.1:g.20331C>T
NC_000001.11:g.20648785C>T
NC_000001.10:g.20975278C>T
More... 		07/10/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PINK1-AS
Accession:NR_046507
Location:EXON;NON-CODING

Gene Symbol:PINK1
Accession:NM_032409
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001587532 CLINVAR
dbSNP (RS) rs144719866 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PINK1 CLINVAR
  PINK1-AS CLINVAR
OMIM 608309 CLINVAR