DPYD NM_000110.4:c.1679T G

Preferred Label : DPYD NM_000110.4:c.1679T G;

NCIt synonyms : DHPDHASE c.1679T G; NM_000110.4:c.1679T G; DHP c.1679T G; Dihydropyrimidine Dehydrogenase c.1679T G; DPYD c.1679T G; DPD c.1679T G; DPYD Polymorphism rs55886062;

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

NCI Metathesaurus CUI : CL1905457;

SNP ID : rs55886062;

Details

Origin ID

C191941;

UMLS CUI

C5784782;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
molecular_abnormality_involves_gene
- DPYD Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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