EGFR NP_005219.2:p.S768_V769insVAS

Preferred Label : EGFR NP_005219.2:p.S768_V769insVAS;

NCIt synonyms : NP_005219.2:p.Ser768_Val769insValAlaSer; Proto-Oncogene c-ErbB-1 S768_V769insVAS; Receptor Tyrosine-Protein Kinase erbB-1 S768_V769insVAS; EGFR p.S768_V769insVAS; EGFR NP_005219.2:p.Ser768_Val769insValAlaSer; Epidermal Growth Factor Receptor S768_V769insVAS; EGFR S768_V769insVAS; NP_005219.2:p.A767_V769dup; NP_005219.2:p.Ala767_Val769dup;

NCIt definition : An insertion of the amino acid sequence valine-alanine-serine between the serine at position 768 and the valine at position 769 of the epidermal growth factor receptor protein.;

Details

Origin ID

C98614;

UMLS CUI

C3274296;

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.2303_2304ins9 [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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