MET NM_000245.3:c.3688T C

Preferred Label : MET NM_000245.3:c.3688T C;

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

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

NCI Metathesaurus CUI : CL970901;

SNP ID : rs121913247;

Details

Origin ID

C162279;

UMLS CUI

C5206486;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
molecular_abnormality_involves_gene
- MET Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

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