EGFR NP_005219.2:p.H773_V774insNPH

Preferred Label : EGFR NP_005219.2:p.H773_V774insNPH;

NCIt synonyms : Proto-Oncogene c-ErbB-1 H773_V774insNPH; Epidermal Growth Factor Receptor H773_V774insNPH; NP_005219.2:p.H773_V774insNPH; EGFR p.H773_V774insNPH; EGFR NP_005219.2:p.His773_Val774insAsnProHis; EGFR H773_V774insNPH; Receptor Tyrosine-Protein Kinase erbB-1 H773_V774insNPH; NP_005219.2:p.His773_Val774insAsnProHis; EGFR Asn771_His773dupAsnProHis; EGFR p.Asn771_His773dupAsnProHis; EGFR p.N771_H773dupNPH; NP_005219.2:p.N771_H773dup; EGFR N771_H773dupNPH; NP_005219.2:p.Asn771_His773dup;

NCIt related terms : EGFR Exon 20 Insertion (N771_H773dupNPH);

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

Details

Origin ID

C98690;

UMLS CUI

C3274361;

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.2319_2320ins9 [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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