EGFR NP_005219.2:p.K29_N298insG

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A deletion of 268 amino acids of the epidermal growth factor receptor protein from the valine at position 30 through the arginine at position 297 followed by the insertion of a glycine between the lysine at position 29 and the asparagine at position 298.

**Synonyms:** - Activating EGFRvIII Mutation - EGFR NP_005219.2:p.Lys29_Asn298insGly - EGFR NP_005219.2:p.V30_R297delK29_N298insG - EGFR NP_005219.2:p.Val30_Arg297delLys29_Asn298insGly - EGFR Variant III - EGFR p. K29_N298insG - EGFR p. Lys29_Asn298insGly - EGFRvIII - EGFRvIII Ectodomain Insertion/Deletion Mutation - EGFRvIII Extracellular Domain Insertion/Deletion Mutation - EGFRvIII Protein Variant - Epidermal Growth Factor Receptor Variant III - Epidermal Growth Factor Receptor vIII - NP_005219.2:p.K29_N298insG - NP_005219.2:p.Lys29_Asn298insGly - NP_005219.2:p.V30_R297delK29_N298insG - NP_005219.2:p.Val30_Arg297delLys29_Asn298insGly - Type III EGF Deletion-Mutant Receptor