RGD:150440892 Rat Genome Database

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Variant: RGD:150440892 -  Homo sapiens

RGD ID: 150440892
RS ID: rs73800218
ClinVar ID: CV1204468
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: QDPR  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 17,492,048
GRCh38 4 17,490,425
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001306140.2:c.536+237C>T
NM_000320.3:c.629+237C>T
NG_008763.1:g.26810C>T
NC_000004.12:g.17490425G>A
More... 		03/29/2019 intron variant likely 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 RCV001583573 CLINVAR
dbSNP (RS) rs73800218 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene QDPR CLINVAR
OMIM 612676 CLINVAR