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EGFR NP_005219.2:p.S768I

MedGen UID:
905289
•Concept ID:
C4086256
•
Cell or Molecular Dysfunction
Synonyms: Activating S768I Mutation; EGFR Exon 20 S768I; EGFR NP_005219.2:p.Ser768Ile; EGFR p.S768I; EGFR p.Ser768Ile; EGFR S768I; EGFR S768I Mutation; EGFR Ser768Ile; Epidermal Growth Factor Receptor S768I; NP_005219.2:p.Ser768Ile; Proto-Oncogene c-ErbB-1 S768I; Receptor Tyrosine-Protein Kinase erbB-1 S768I

Definition

A change in the amino acid residue at position 768 in the epidermal growth factor receptor protein where serine has been replaced by isoleucine. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVEGFR NP_005219.2:p.S768I

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