EGFR NM_005228.3:c.2156delG

Preferred Label : EGFR NM_005228.3:c.2156delG;

NCIt synonyms : Epidermal Growth Factor Receptor Gene c.2156delG; HER1 c.2156delG; ERBB c.2156delG; ERBB1 c.2156delG; NM_005228.3:c.2156delG; EGFR c.2156delG; EGFR NM_005228.3:c.2156del; NM_005228.3:c.2156del;

NCIt definition : A deletion of a guanine at position 2156 from the coding sequence of the EGFR gene.;

Details

Origin ID

C98533;

UMLS CUI

C3274222;

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.G719fs*29 [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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