MET Exon 14 Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A molecular genetic abnormality indicating the presence of a mutation in exon 14 of the MET gene located in the vicinity of 7q31.

**Synonyms:** - HGFR Exon 14 Mutation - MET Proto-Oncogene, Receptor Tyrosine Kinase Exon 14 Mutation - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Mutation - c-Met Exon 14 Mutation