RGD:8646526 Rat Genome Database

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Variant: RGD:8646526 -  Homo sapiens

RGD ID: 8646526
RS ID: rs115632870
ClinVar ID: CV105999
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DPYD  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 98,293,821
GRCh38 1 97,828,265
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001160301.1:c.151-69G>A
NG_008807.2:g.97795G>A
NC_000001.11:g.97828265C>T
NC_000001.9:g.98066409C>T
More... 		07/22/2021 intron variant likely benign|not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:DPYD
Accession:XM_047448076
Location:5UTRS;INTRON

Gene Symbol:DPYD
Accession:XM_017000507
Location:INTRON

Gene Symbol:DPYD
Accession:XM_047448077
Location:INTRON

Gene Symbol:DPYD
Accession:NM_001160301
Location:INTRON

Gene Symbol:DPYD
Accession:XM_006710397
Location:INTRON

Gene Symbol:DPYD
Accession:NM_000110
Location:INTRON

Gene Symbol:DPYD
Accession:XM_005270562
Location:INTRON

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

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000086505 CLINVAR
  RCV003964962 CLINVAR
dbSNP (RS) rs115632870 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DPYD CLINVAR
OMIM 612779 CLINVAR