C162302Level 6
MET NM_000245.3:c.1915A>C
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A nucleotide substitution at position 1915 of the coding sequence of the MET gene where adenine has been mutated to cytosine.
**Synonyms:** - HGFR c.1915A>C - MET Proto-Oncogene, Receptor Tyrosine Kinase c.1915A>C - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) c.1915A>C - NM_000245.3:c.1915A>C - NM_001127500.2:c.1915A>C - c-Met c.1915A>C
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Cross-system equivalences0
No cross-system equivalences mapped for this node.