EGFR NP_005219.2:p.V774_C775insHV

Preferred Label : EGFR NP_005219.2:p.V774_C775insHV;

NCIt synonyms : NP_005219.2:p.V774_C775insHV; NP_005219.2:p.Val774_Cys775insHisVal; EGFR V774_C775insHV; EGFR p.V774_C775insHV; Proto-Oncogene c-ErbB-1 V774_C775insHV; Receptor Tyrosine-Protein Kinase erbB-1 V774_C775insHV; EGFR NP_005219.2:p.Val774_Cys775insHisVal; Epidermal Growth Factor Receptor V774_C775insHV; NP_005219.2:p.H773_V774dup; NP_005219.2:p.His773_Val774dup;

NCIt definition : An insertion of the amino acid sequence histidine-valine between the valine at position 774 and the cysteine at position 775 of the epidermal growth factor receptor protein.;

Details

Origin ID

C98695;

UMLS CUI

C3274366;

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.2316_2321dup [NCIt concept]
- EGFR NM_005228.3:c.2321_2322insCCACGT [NCIt concept]
- EGFR NM_005228.3:c.2322_2323insCACGTG [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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