EGFR NP_005219.2:p.H773_V774insH

Preferred Label : EGFR NP_005219.2:p.H773_V774insH;

NCIt synonyms : EGFR NP_005219.2:p.His773_Val774insHis; NP_005219.2:p.His773_Val774insHis; NP_005219.2:p.H773_V774insH; Proto-Oncogene c-ErbB-1 H773_V774insH; Epidermal Growth Factor Receptor H773_V774insH; Receptor Tyrosine-Protein Kinase erbB-1 H773_V774insH; EGFR H773_V774insH; EGFR p.H773_V774insH; NP_005219.2:p.His773dup; NP_005219.2:p.H773dup;

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

Details

Origin ID

C98688;

UMLS CUI

C3274359;

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_2320insCAC [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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