EGFR NP_005219.2:p.H773_V774insAH

Preferred Label : EGFR NP_005219.2:p.H773_V774insAH;

NCIt synonyms : Receptor Tyrosine-Protein Kinase erbB-1 H773_V774insAH; Proto-Oncogene c-ErbB-1 H773_V774insAH; EGFR p.H773_V774insAH; Epidermal Growth Factor Receptor H773_V774insAH; NP_005219.2:p.H773_V774insAH; EGFR H773_V774insAH; EGFR NP_005219.2:p.His773_Val774insAlaHis; Receptor Tyrosine-Protein Kinase erbB-1 His773_Val774insAlaHis; Proto-Oncogene c-ErbB-1 His773_Val774insAlaHis; EGFR p.His773_Val774insAlaHis; Epidermal Growth Factor Receptor His773_Val774insAlaHis; NP_005219.2:p.His773_Val774insAlaHis; EGFR His773_Val774insAlaHis;

NCIt definition : An insertion of the amino acid sequence alanine-histidine between the histidine at position 773 and the valine at position 774 of the epidermal growth factor receptor protein.;

NCI Metathesaurus CUI : CL526380;

Details

Origin ID

C138924;

UMLS CUI

C4528145;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
gene_product_sequence_variation_encoded_by_gene_mutant
- EGFR Gene Mutation [NCIt concept]
- EGFR NM_005228.3:c.2320_2321insCCCACG [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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