Thymidine to Guanosine Transversion Abnormality

MedGen UID:: 328112
•Concept ID:: C1710406
•: Cell or Molecular Dysfunction

Synonyms:

Thymidine to Guanosine Mutation; Thymidine to Guanosine Transversion

Definition

A point mutation involving the substitution of Guanosine (a purine base) for Thymidine (a pyrimidine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVThymidine to Guanosine Transversion Abnormality

Molecular Abnormality
- Molecular Sequence Variation
  - Molecular Genetic Variation
    - Mutation Abnormality
      - Point mutation
        Transversion Mutation
        Thymidine to Guanosine Transversion Abnormality

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Thymidine to Guanosine Transversion Abnormality

Definition

Term Hierarchy

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