C45656Level 6
Multiple Transition Abnormalities
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** Multiple point mutations in a DNA sequence from eukaryotic or prokaryotic organisms in which each mutation occurs by substitution of a purine base for a different purine base or a pyrimidine base for another pyrimidine base. These abnormalities can be either heritable or occur somatically.
**Synonyms:** - Multiple Transition Mutations - Transition Mutations
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