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     
-/. - c.775A>G r.(?) p.(Lys259Glu) - - benign g.98144726T>C g.97679170T>C DPYD(NM_000110.3):c.775A>G (p.K259E) - DPYD_000043 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
?/. - c.775A>G r.(?) p.(Lys259Glu) - - VUS g.98144726T>C g.97679170T>C DPYD(NM_000110.3):c.775A>G (p.K259E) - DPYD_000043 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Utrecht
-?/. - c.775A>G r.(?) p.(Lys259Glu) - - likely benign g.98144726T>C g.97679170T>C - - DPYD_000043 21 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs45589337 Germline - 21/2773 individuals - 0 - Mohammed Faruq
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