EGFR NP_005219.2:p.G719X

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the amino acid residue at position 719 in the epidermal growth factor receptor protein where glycine has been replaced by another amino acid.

**Synonyms:** - Activating G719X Mutation - EGFR G719 Mutation - EGFR G719X - EGFR Gly719Xxx - EGFR NP_005219.2:p.Gly719Xxx - EGFR exon 18 G719X - EGFR p.G719X - Epidermal Growth Factor Receptor G719X - Exon 18 Gly719 - NP_005219.2:p.G719X - NP_005219.2:p.Gly719Xxx - Proto-Oncogene c-ErbB-1 G719X - Receptor Tyrosine-Protein Kinase erbB-1 G719X