MET Codon 1010 Splice Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of MET gene that alters splicing at codon 1010.

**Synonyms:** - HGFR Codon 1010 Splice Mutation - MET Asp1010 Splice Mutation - MET D1010 Splice Mutation - MET D1010_splice mutation detected - MET Proto-Oncogene, Receptor Tyrosine Kinase Codon 1010 Splice Mutation - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Codon 1010 Splice Mutation - c-Met Codon 1010 Splice Mutation