EGFR NP_005219.2:p.S768I

Preferred Label : EGFR NP_005219.2:p.S768I;

NCIt synonyms : EGFR S768I; Epidermal Growth Factor Receptor S768I; EGFR p.S768I; NP_005219.2:p.Ser768Ile; EGFR Ser768Ile; EGFR p.Ser768Ile; Proto-Oncogene c-ErbB-1 S768I; Receptor Tyrosine-Protein Kinase erbB-1 S768I; EGFR NP_005219.2:p.Ser768Ile; EGFR Exon 20 S768I; EGFR S768I Mutation; Activating S768I Mutation;

NCIt definition : A change in the amino acid residue at position 768 in the epidermal growth factor receptor protein where serine has been replaced by isoleucine.;

Details

Origin ID

C125210;

UMLS CUI

C4086256;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Disease 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.2303G>T [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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