C45651Level 7
Cytosine to Guanosine Transversion Abnormality
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation involving the substitution of Guanosine (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 Guanosine Mutation - Cytosine to Guanosine Transversion
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