EGFR NP_005219.2:p.S768_V769insVAS

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** An insertion of the amino acid sequence valine-alanine-serine between the serine at position 768 and the valine at position 769 of the epidermal growth factor receptor protein.

**Synonyms:** - EGFR A767_V769 Duplication Mutation - EGFR NP_005219.2:p.A767_V769dup - EGFR NP_005219.2:p.Ser768_Val769insValAlaSer - EGFR S768_V769insVAS - EGFR p.S768_V769insVAS - Epidermal Growth Factor Receptor S768_V769insVAS - NP_005219.2:p.A767_V769dup - NP_005219.2:p.Ala767_Val769dup - NP_005219.2:p.Ser768_Val769insValAlaSer - Proto-Oncogene c-ErbB-1 S768_V769insVAS - Receptor Tyrosine-Protein Kinase erbB-1 S768_V769insVAS