C162285Level 6
MET NM_000245.3:c.3613T>G
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A nucleotide substitution at position 3613 of the coding sequence of the MET gene where thymine has been mutated to guanine.
**Synonyms:** - HGFR c.3613T>G - MET Proto-Oncogene, Receptor Tyrosine Kinase c.3613T>G - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) c.3613T>G - NM_000245.3:c.3613T>G - NM_001127500.2:c.3667T>G - c-Met c.3613T>G
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Cross-system equivalences0
No cross-system equivalences mapped for this node.