EGFR NP_005219.2:p.A767_S768insTLA

Preferred Label : EGFR NP_005219.2:p.A767_S768insTLA;

NCIt synonyms : EGFR p.A767_S768insTLA; Receptor Tyrosine-Protein Kinase erbB-1 A767_S768insTLA; NP_005219.2:p.Ala767_Ser768insThrLeuAla; Epidermal Growth Factor Receptor A767_S768insTLA; Proto-Oncogene c-ErbB-1 A767_S768insTLA; EGFR A767_S768insTLA; EGFR NP_005219.2:p.Ala767_Ser768insThrLeuAla;

NCIt definition : An insertion of the amino acid sequence threonine-leucine-alanine between the alanine at position 767 and the serine at position 768 of the epidermal growth factor receptor protein.;

Details

Origin ID

C98608;

UMLS CUI

C3274291;

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.2302_2303ins9 [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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