C147123Level 7
MET Codon 963 Splice Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the nucleotide sequence of MET gene that alters splicing at codon 963.
**Synonyms:** - HGFR Codon 963 Splice Mutation - MET Asp963 Splice Mutation - MET D963 Splice Mutation - MET D963_splice mutation detected - MET Proto-Oncogene, Receptor Tyrosine Kinase Codon 963 Splice Mutation - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Codon 963 Splice Mutation - c-Met Codon 963 Splice Mutation
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