C45650Level 7
Cytosine to Adenosine Transversion Abnormality
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation involving the substitution of Adenosine (a purine base) for Cytosine (a pyrimidine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically.
**Synonyms:** - Cytosine to Adenosine Mutation - Cytosine to Adenosine Transversion
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