RGD:150499139 Rat Genome Database

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Variant: RGD:150499139 -  Homo sapiens

RGD ID: 150499139
RS ID: rs3733573
ClinVar ID: CV1254310
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: QDPR  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 17,503,561
GRCh38 4 17,501,938
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.17501938T>C
NC_000004.11:g.17503561T>C
NM_001306140.2:c.203-79A>G
NM_000320.3:c.296-79A>G
More... 		09/22/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:QDPR
Accession:NM_001306140
Location:INTRON

Gene Symbol:QDPR
Accession:NM_000320
Location:INTRON

Gene Symbol:QDPR
Accession:NR_156494
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001676484 CLINVAR
dbSNP (RS) rs3733573 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene QDPR CLINVAR
OMIM 612676 CLINVAR