World Of Taxonomy
C136642Level 7

Non-synonymous VEGFR Family Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A point mutation in a gene that is a member of the VEGFR gene family that encodes an amino acid substitution in a VEGFR family protein.

**Synonyms:** - Non-synonymous Vascular Endothelial Growth Factor Receptor Family Gene Mutation - VEGFR Family Gene Missense Mutation

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