EGFR NP_005219.2:p.K745_A750del

MedGen UID:: 475856
•Concept ID:: C3274223
•: Cell or Molecular Dysfunction

Synonyms:

EGFR K745_A750del; EGFR NP_005219.2:p.Lys745_Ala750del; EGFR p.K745_A750del; Epidermal Growth Factor Receptor p.K745_A750del; NP_005219.2:p.Lys745_Ala750del; Proto-Oncogene c-ErbB-1 p.K745_A750del; Receptor Tyrosine-Protein Kinase erbB-1 p.K745_A750del

Definition

A deletion of six amino acids from the epidermal growth factor receptor protein from the lysine at position 745 through the alanine at position 750. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVEGFR NP_005219.2:p.K745_A750del

Molecular Abnormality
- Molecular Sequence Variation
  - Gene Product Sequence Variation
    - EGFR Protein Variant
      - EGFR NP_005219.2:p.K745_A750del

Supplemental Content

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