EGFR NP_005219.2:p.M766_A767insAI

Preferred Label : EGFR NP_005219.2:p.M766_A767insAI;

NCIt synonyms : Epidermal Growth Factor Receptor M766_A767insAI; EGFR p.M766_A767insAI; EGFR NP_005219.2:p.Met766_Ala767insAlaIle; EGFR M766_A767insAI; NP_005219.2:p.Met766_Ala767insAlaIle; Receptor Tyrosine-Protein Kinase erbB-1 M766_A767insAI; Proto-Oncogene c-ErbB-1 M766_A767insAI; NP_005219.2:p.M766_A767insAI;

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

Details

Origin ID

C98606;

UMLS CUI

C3274289;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_product_sequence_variation_encoded_by_gene_mutant
- EGFR Gene Mutation [NCIt concept]
- EGFR NM_005228.3:c.2298_2299insGCCATA [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) :

You can consult :

recommendations
documents concerning education
documents for patients