DPYD NM_000110.4:c.1679T>G

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1679 of the coding sequence of the DPYD gene where thymine has been mutated to guanine.

**Synonyms:** - DHP c.1679T>G - DHPDHASE c.1679T>G - DPD c.1679T>G - DPYD Polymorphism rs55886062 - DPYD c.1679T>G - Dihydropyrimidine Dehydrogenase c.1679T>G - NM_000110.4:c.1679T>G