EGFR NP_005219.2:p.M766_A767insASV

Preferred Label : EGFR NP_005219.2:p.M766_A767insASV;

NCIt synonyms : NP_005219.2:p.M766_A767insASV; EGFR M766_A767insASV; Epidermal Growth Factor Receptor M766_A767insASV; EGFR p.M766_A767insASV; Proto-Oncogene c-ErbB-1 M766_A767insASV; NP_005219.2:p.Met766_Ala767insAlaSerVal; EGFR Met766_Ala767insAlaSerVal; Epidermal Growth Factor Receptor Met766_Ala767insAlaSerVal; EGFR p.Met766_Ala767insAlaSerVal; Proto-Oncogene c-ErbB-1 Met766_Ala767insAlaSerVal; Receptor Tyrosine-Protein Kinase erbB-1 Met766_Ala767insAlaSerVal; EGFR NP_005219.2:p.Met766_Ala767insAlaSerVal;

NCIt definition : An insertion of the amino acid sequence alanine-serine-valine between the methionine at position 766 and the alanine at position 767 of the epidermal growth factor receptor protein.;

NCI Metathesaurus CUI : CL526392;

Details

Origin ID

C138903;

UMLS CUI

C4528126;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
gene_product_sequence_variation_encoded_by_gene_mutant
- EGFR Gene Mutation [NCIt concept]
gene_product_variant_of_gene_product
- Epidermal Growth Factor Receptor [NCIt concept]
molecular_abnormality_involves_gene
- EGFR Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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