RGD:150420931 Rat Genome Database

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Variant: RGD:150420931 -  Homo sapiens

RGD ID: 150420931
RS ID: rs758202034
ClinVar ID: CV1181535
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PNPO  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 46,023,976
GRCh38 17 47,946,610
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018129.4:c.618-4A>G
NG_008744.1:g.10088A>G
NC_000017.11:g.47946610A>G
NC_000017.10:g.46023976A>G
 07/21/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PNPO
Accession:NM_018129
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001551782 CLINVAR
dbSNP (RS) rs758202034 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PNPO CLINVAR
OMIM 603287 CLINVAR