Guanosine to Cytosine Transversion Abnormality

MedGen UID:: 313240
•Concept ID:: C1708262
•: Cell or Molecular Dysfunction

Synonyms:

Guanosine to Cytosine Mutation; Guanosine to Cytosine Transversion

Definition

A point mutation involving the substitution of Cytosine (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. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVGuanosine to Cytosine Transversion Abnormality

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

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Guanosine to Cytosine Transversion Abnormality

Definition

Term Hierarchy

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