MET NM_000245.3:c.3708T>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 3708 of the coding sequence of the MET gene where thymine has been mutated to adenine.

**Synonyms:** - HGFR c.3708T>A - MET Proto-Oncogene, Receptor Tyrosine Kinase c.3708T>A - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) c.3708T>A - NM_000245.3:c.3708T>A - c-Met c.3708T>A