EGFR NP_005219.2:p.P772_H773insNPH

Preferred Label : EGFR NP_005219.2:p.P772_H773insNPH;

NCIt synonyms : EGFR P772_H773insNPH; NP_005219.2:p.P772_H773insNPH; Epidermal Growth Factor Receptor P772_H773insNPH; EGFR p.P772_H773insNPH; Proto-Oncogene c-ErbB-1 P772_H773insNPH; Receptor Tyrosine-Protein Kinase erbB-1 P772_H773insNPH; EGFR Pro772_His773insAsnProHis; NP_005219.2:p.Pro772_His773insAsnProHis; Epidermal Growth Factor Receptor Pro772_His773insAsnProHis; EGFR p.Pro772_His773insAsnProHis; Proto-Oncogene c-ErbB-1 Pro772_His773insAsnProHis; Receptor Tyrosine-Protein Kinase erbB-1 Pro772_His773insAsnProHis; EGFR NP_005219.2:p.Pro772_His773insAsnProHis;

NCIt definition : An insertion of the amino acid sequence asparagine-proline-histidine between the proline at position 772 and the histidine at position 773 of the epidermal growth factor receptor protein.;

NCI Metathesaurus CUI : CL526398;

Details

Origin ID

C138911;

UMLS CUI

C4528714;

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) :

You can consult :

recommendations
documents concerning education
documents for patients