EGFR NM_005228.3:c.2236_2253del18

Preferred Label : EGFR NM_005228.3:c.2236_2253del18;

NCIt synonyms : ERBB1 c.2236_2253del18; EGFR c.2236_2253del18; NM_005228.3:c.2236_2253del18; NM_005228.3:c.2236_2253delGAATTAAGAGAAGCAACA; HER1 c.2236_2253del18; EGFR NM_005228.3:c.2236_2253delGAATTAAGAGAAGCAACA; ERBB c.2236_2253del18; Epidermal Growth Factor Receptor Gene c.2236_2253del18; NM_005228.3:c.2236_2253del;

NCIt definition : A deletion of 18 nucleotides from the coding sequence of the EGFR gene from position 2236 through 2253.;

SNP ID : rs121913426;

Details

Origin ID

C98548;

UMLS CUI

C3274236;

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_mutant_encodes_gene_product_sequence_variation
- EGFR NP_005219.2:p.E746_T751del [NCIt concept]
- EGFR Protein Variant [NCIt concept]
molecular_abnormality_involves_gene
- EGFR Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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