Cytosine to Thymidine Transition Abnormality

Preferred Label : Cytosine to Thymidine Transition Abnormality;

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

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

Details

Origin ID

C45643;

UMLS CUI

C1707606;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
abnormality_associated_with_allele
- CYP2C19*10 Allele [NCIt concept]
- CYP2C19*5 Allele [NCIt concept]
- CYP2C8*7 Allele [NCIt concept]
- CYP2C9*11 Allele [NCIt concept]
- CYP2C9*12 Allele [NCIt concept]
- CYP2C9*2 Allele [NCIt concept]
- CYP2D6*10 Allele [NCIt concept]
- CYP2D6*17 Allele [NCIt concept]
- CYP2D6*2 Allele [NCIt concept]
- CYP2D6*36 Allele [NCIt concept]
- CYP2D6*41 Allele [NCIt concept]
- CYP3A5*8 Allele [NCIt concept]
- NQO1*2 Allele [NCIt concept]

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