EGFR NP_005219.2:p.A750_E758del

MedGen UID:: 475889
•Concept ID:: C3274256
•: Cell or Molecular Dysfunction

Synonyms:

EGFR A750_E758del; EGFR NP_005219.2:p.Ala750_Glu758del; EGFR p.A750_E758del; Epidermal Growth Factor Receptor A750_E758del; NP_005219.2:p.Ala750_Glu758del; Proto-Oncogene c-ErbB-1 A750_E758del; Receptor Tyrosine-Protein Kinase erbB-1 A750_E758del

Definition

A deletion of nine amino acids from the epidermal growth factor receptor protein from the alanine at position 750 through the glutamic acid at position 758. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVEGFR NP_005219.2:p.A750_E758del

Molecular Abnormality
- Molecular Sequence Variation
  - Gene Product Sequence Variation
    - EGFR Protein Variant
      - EGFR NP_005219.2:p.A750_E758del

Supplemental Content

Practice guidelines

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