rs7517357 Rat Genome Database

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Variant: rs7517357 -  Homo sapiens

RGD ID: 150503358
RS ID: rs7517357
ClinVar ID: CV1257779
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PARK7  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 8,025,275
GRCh38 1 7,965,215
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001123377.2:c.91-109C>T
NM_007262.5:c.91-109C>T
NG_008271.1:g.8562C>T
NC_000001.11:g.7965215C>T
More... 		08/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PARK7
Accession:NM_007262
Location:INTRON

Gene Symbol:PARK7
Accession:XM_005263424
Location:INTRON

Gene Symbol:PARK7
Accession:NM_001123377
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001677467 CLINVAR
dbSNP (RS) rs7517357 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PARK7 CLINVAR
OMIM 602533 CLINVAR