C162298Level 6
MET NM_000245.3:c.3209T>A
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A nucleotide substitution at position 3209 of the coding sequence of the MET gene where thymine has been mutated to adenine.
**Synonyms:** - HGFR c.3209T>A - MET Proto-Oncogene, Receptor Tyrosine Kinase c.3209T>A - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) c.3209T>A - NM_000245.3:c.3209T>A - NM_001127500.2:c.3263T>A - c-Met c.3209T>A
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Cross-system equivalences0
No cross-system equivalences mapped for this node.