MET NM_000245.3:c.3688T>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 3688 of the coding sequence of the MET gene where thymine has been mutated to cytosine.

**Synonyms:** - HGFR c.3688T>C - MET Proto-Oncogene, Receptor Tyrosine Kinase c.3688T>C - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) c.3688T>C - NM_000245.3:c.3688T>C - NM_001127500.2:c.3742T>C - c-Met c.3688T>C