RGD:150475856 Rat Genome Database

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Variant: RGD:150475856 -  Homo sapiens

RGD ID: 150475856
RS ID: rs1337752
ClinVar ID: CV1271252
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DPYD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 97,981,706
GRCh38 1 97,516,150
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000110.4:c.1525-209G>A
LRG_722:g.409910G>A
NG_008807.2:g.409910G>A
NC_000001.11:g.97516150C>T
More... 		07/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DPYD
Accession:NM_001160301
Location:INTRON

Gene Symbol:DPYD
Accession:XM_006710397
Location:INTRON

Gene Symbol:DPYD
Accession:XM_047448077
Location:INTRON

Gene Symbol:DPYD
Accession:XM_005270562
Location:INTRON

Gene Symbol:DPYD
Accession:XM_017000507
Location:INTRON

Gene Symbol:DPYD
Accession:XM_047448076
Location:INTRON

Gene Symbol:DPYD
Accession:NM_000110
Location:INTRON

Gene Symbol:DPYD
Accession:XR_001737014
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001696075 CLINVAR
dbSNP (RS) rs1337752 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DPYD CLINVAR
OMIM 612779 CLINVAR