EGFR NP_005219.2:p.D770_N771insSVD

Preferred Label : EGFR NP_005219.2:p.D770_N771insSVD;

NCIt synonyms : Proto-Oncogene c-ErbB-1 D770_N771insSVD; EGFR D770_N771insSVD; EGFR NP_005219.2:p.Asp770_Asn771insSerValAsp; EGFR p.D770_N771insSVD; Epidermal Growth Factor Receptor D770_N771insSVD; NP_005219.2:p.D770_N771insSVD; Receptor Tyrosine-Protein Kinase erbB-1 D770_N771insSVD; NP_005219.2:p.Asp770_Asn771insSerValAsp; NP_005219.2:p.S768_D770dup; NP_005219.2:p.Ser768_Asp770dup; EGFR p. Asn771_Pro772 SerValAspAsnPro; EGFR p.S768_D770dupSVD; EGFR Asn771_Pro772 SerValAspAsnPro; EGFR N771_P772 SVDNP; EGFR p.Ser768_Asp770dupSerValAsp; EGFR S768_D770dupSVD; EGFR Ser768_Asp770dupSerValAsp; EGFR p.N771_P772 SVDNP;

NCIt related terms : EGFR Exon 20 Insertion (N771_P772 SVDNP); EGFR Exon 20 Insertion (S768_D770dupSVD); EGFR Exon 20 Insertion (D770_N771insSVD);

NCIt definition : An insertion of the amino acid sequence serine-valine-aspartic acid between the aspartic acid at position 770 and the asparagine at position 771 of the epidermal growth factor receptor protein.;

Details

Origin ID

C98658;

UMLS CUI

C3274333;

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.2310_2311insAGCGTGGAC [NCIt concept]
- EGFR NM_005228.3:c.2311_2312ins9 [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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