MET NM_000245.3:c.3689A>G

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 3689 of the coding sequence of the MET gene where adenine has been mutated to guanine.

**Synonyms:** - HGFR c.3689A>G - MET Proto-Oncogene, Receptor Tyrosine Kinase c.3689A>G - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) c.3689A>G - NM_000245.3:c.3689A>G - NM_001127500.2:c.3743A>G - c-Met c.3689A>G