All variants in the DPYD gene

Information The variants shown are described using the NM_000110.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Haplotype     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/- 21 c.2657G= r.2657g= p.Arg886= DPYD*1 - benign g.97564154C= - - - DPYD_000000 reference haplotype DPYD*1 [85T=; 2657G=]; note the reference sequence has haplotype DPYD*9A Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. PubMed: McLeod 1998 - - Germline - - - 0 - Johan den Dunnen
-/- 21 c.2657G= r.2657g= p.Arg886= DPYD*9A - benign g.97564154C= - - - DPYD_000000 reference haplotype DPYD*9A [85T>C; 2657G=]; note the reference sequence has haplotype DPYD*9A Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. PubMed: McLeod 1998 - - Germline - - - 0 - Johan den Dunnen
-?/. 21 c.2657G= r.(=) p.Arg886= DPYD*9A - likely benign g.97564154C= - - - DPYD_000000 normal enzyme activity (PBM cells) Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message. PubMed: Johnson 2002 - - Unknown - - - 0 - Johan den Dunnen
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