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PIK3CA NM_006218.1:c.3140A>T

MedGen UID:: 475762
•Concept ID:: C3274129
•: Cell or Molecular Dysfunction

Synonyms:

NM_006218.1:c.3140A>T; p110-alpha c.3140A>T; Phosphoinositide-3-Kinase, Catalytic, Alpha Polypeptide c.3140A>T; PI3K c.3140A>T; PIK3CA c.3140A>T

Definition

A nucleotide substitution at position 3140 of the coding sequence of the PIK3CA gene where adenine has been mutated to thymine. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVPIK3CA NM_006218.1:c.3140A>T

Molecular Genetic Variation
- Gene Abnormality
  - PI3K/MTOR Pathway Mutation
    - PI3K Gene Mutation
      - PIK3CA Gene Mutation
        PIK3CA Exon 20 Mutation
        PIK3CA NM_006218.1:c.3140A>T

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