EGFR NP_005219.2:p.S768_V769insAWT

Preferred Label : EGFR NP_005219.2:p.S768_V769insAWT;

NCIt synonyms : EGFR S768_V769insAWT; Epidermal Growth Factor Receptor S768_V769insAWT; NP_005219.2:p.Ser768_Val769insAlaTrpThr; EGFR NP_005219.2:p.Ser768_Val769insAlaTrpThr; EGFR p.S768_V769insAWT; Receptor Tyrosine-Protein Kinase erbB-1 S768_V769insAWT; Proto-Oncogene c-ErbB-1 S768_V769insAWT;

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

Details

Origin ID

C98613;

UMLS CUI

C3274295;

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]
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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