RGD:8646484 Rat Genome Database

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Variant: RGD:8646484 -  Homo sapiens

RGD ID: 8646484
RS ID: rs672601280
ClinVar ID: CV105958
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DPYD  DPYD-AS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 97,770,978
GRCh38 1 97,305,422
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008807.2:g.620638T>C
NC_000001.11:g.97305422A>G
NC_000001.9:g.97543566A>G
NC_000001.10:g.97770978A>G
More... 		intron variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:DPYD
Accession:XM_005270562
Location:INTRON

Gene Symbol:DPYD
Accession:XM_017000507
Location:INTRON

Gene Symbol:DPYD
Accession:XM_047448077
Location:INTRON

Gene Symbol:DPYD
Accession:NM_000110
Location:INTRON

Gene Symbol:DPYD
Accession:XM_006710397
Location:INTRON

Gene Symbol:DPYD
Accession:NM_001160301
Location:INTRON

Gene Symbol:DPYD
Accession:XM_047448076
Location:INTRON

Gene Symbol:DPYD-AS1
Accession:NR_046590
Location:INTRON;NON-CODING

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000086463 CLINVAR
dbSNP (RS) rs672601280 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene DPYD CLINVAR
  DPYD-AS1 CLINVAR
OMIM 612779 CLINVAR