MET Exon 14 Skipping Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A molecular genetic abnormality indicating the presence of a splice site mutation that results in a loss of transcription of exon 14 of the MET gene.

**Synonyms:** - Deletion of MET Exon 14 - Deletion of c-MET Exon 14 - HGFR Exon 14 Skipping Alteration - HGFR Exon 14 Skipping Mutation - HGFR Exon 14 Splice Mutation - Loss of MET Exon 14 - Loss of c-MET Exon 14 - MET Exon 14 Deletion Mutation - MET Exon 14 Skipping Alteration - MET Exon 14 Splice Mutation - MET Proto-Oncogene, Receptor Tyrosine Kinase Exon 14 Skipping Alteration - MET Proto-Oncogene, Receptor Tyrosine Kinase Exon 14 Skipping Mutation - MET exon 14 deletion detected - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Skipping Alteration - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Skipping Mutation - Met Proto-Oncogene (Hepatocyte Growth Factor Receptor) Exon 14 Splice Mutation - c-MET Exon 14 Deletion Mutation - c-MET Exon 14 Splice Mutation - c-Met Exon 14 Skipping Alteration - c-Met Exon 14 Skipping Mutation