C45646Level 7
Guanosine to Thymidine Transversion Abnormality
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation involving the substitution of Thymidine (a pyrimidine base) for Guanosine (a purine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically.
**Synonyms:** - Guanosine to Thymidine Mutation - Guanosine to Thymidine Transversion
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