EGFR NP_005219.2:p.V769M

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the amino acid residue at position 769 in the epidermal growth factor receptor protein where valine has been replaced by methionine.

**Synonyms:** - Activating V769M Mutation - EGFR NP_005219.2:p.Val769Met - EGFR V769M - EGFR V769M Mutation - EGFR Val769Met - EGFR p.V769M - EGFR p.Val769Met - Epidermal Growth Factor Receptor V769M - Epidermal Growth Factor Receptor Val769Met - NP_005219.2:p.V769M - NP_005219.2:p.Val769Met - Proto-Oncogene c-ErbB-1 V769M - Proto-Oncogene c-ErbB-1 Val769Met - Receptor Tyrosine-Protein Kinase erbB-1 V769M - Receptor Tyrosine-Protein Kinase erbB-1 Val769Met