Thymidine to Cytosine Transition Abnormality

Preferred Label : Thymidine to Cytosine Transition Abnormality;

NCIt synonyms : Thymidine to Cytosine Mutation; Thymidine to Cytosine Transition;

NCIt definition : A point mutation involving the substitution of Cytosine (a pyrimidine base) for Thymidine (a pyrimidine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically.;

Details

Origin ID

C45642;

UMLS CUI

C1710405;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
abnormality_associated_with_allele
- CYP2C19*8 Allele [NCIt concept]
- CYP2C9*1 Allele [NCIt concept]
- CYP3A4*17 Allele [NCIt concept]
- CYP3A4*18 Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients