All variants in the DPYD gene

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

2 entries on 1 page. Showing entries 1 - 2.
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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.1896T>C r.(=) p.(=) - - likely benign g.97915624A>G g.97450068A>G - - DPYD_000052 204 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs17376848 Germline - 204/2795 individuals - 0 - Mohammed Faruq
-?/. - c.1896T>C r.(=) p.(=) - - likely benign g.97915624A>G g.97450068A>G - - DPYD_000052 4 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs17376848 Germline - 4/2795 individuals - 0 - Mohammed Faruq
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