EGFR NP_005219.2:p.V769_D770insASV

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** An insertion of the amino acid sequence alanine-serine-valine between the valine at position 769 and the aspartic acid at position 770 of the epidermal growth factor receptor protein.

**Synonyms:** - EGFR A767_V769 Duplication Mutation - EGFR A767_V769dupASV - EGFR Ala767_Val769dupAlaSerVal - EGFR Asp770_Asn771>AlaSerValAspAsn - EGFR D770_N771>ASVDN - EGFR Exon 20 Insertion (A767_V769dupASV) - EGFR Exon 20 Insertion (D770_N771>ASVDN) - EGFR Exon 20 Insertion (V769_D770insASV) - EGFR NP_005219.2:p.A767_V769dup - EGFR NP_005219.2:p.Val769_Asp770insAlaSerVal - EGFR V769_D770insASV - EGFR p.A767_V769dupASV - EGFR p.Ala767_Val769dupAlaSerVal - EGFR p.V769_D770insASV - Epidermal Growth Factor Receptor V769_D770insASV - NP_005219.2:p.A767_V769dup - NP_005219.2:p.Ala767_Val769dup - NP_005219.2:p.Val769_Asp770insAlaSerVal - Proto-Oncogene c-ErbB-1 V769_D770insASV - Receptor Tyrosine-Protein Kinase erbB-1 V769_D770insASV