Non-synonymous FBXW7 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A point mutation in the FBXW7 gene that encodes an amino acid substitution in the F-box/WD repeat-containing protein 7 protein.

**Synonyms:** - FBXW7 Missense Gene Mutation - FBXW7 Missense Mutation - Non-synonymous AGO Gene Mutation - Non-synonymous Archipelago Homolog Gene Mutation - Non-synonymous Archipelago Homolog, Drosophila Gene Mutation - Non-synonymous CDC4 Gene Mutation - Non-synonymous F-Box and WD Repeat Domain Containing 7 Gene Mutation - Non-synonymous F-box and WD-40 Domain Protein 7 (Archipelago Homolog, Drosophila) Gene Mutation - Non-synonymous FBW6 Gene Mutation - Non-synonymous FBW7 Gene Mutation - Non-synonymous FBX30 Gene Mutation - Non-synonymous FBXW6 Gene Mutation - Non-synonymous SEL-10 Gene Mutation - Non-synonymous SEL10 Gene Mutation