EGFR NM_005228.3:c.2240_2254del15

Preferred Label : EGFR NM_005228.3:c.2240_2254del15;

NCIt synonyms : Epidermal Growth Factor Receptor Gene c.2240_2254del15; ERBB1 c.2240_2254del15; NM_005228.3:c.2240_2254delTAAGAGAAGCAACAT; EGFR NM_005228.3:c.2240_2254delTAAGAGAAGCAACAT; NM_005228.3:c.2240_2254del15; HER1 c.2240_2254del15; EGFR c.2240_2254del15; ERBB c.2240_2254del15; NM_005228.3:c.2240_2254del;

NCIt definition : A deletion of 15 nucleotides from the coding sequence of the EGFR gene from position 2240 through 2254.;

SNP ID : rs121913442;

Details

Origin ID

C98563;

UMLS CUI

C3274251;

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.L747_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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