EGFR NM_005228.3:c.2309_2310delinsCCAGCGTGGAT
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A complex substitution where the deletion of the nucleotide sequence adenine-cytosine at positions 2309 and 2310 of the coding sequence of the EGFR gene is followed by the insertion of 11 nucleotides, CCAGCGTGGAT.
**Synonyms:** - EGFR NM_005228.3:c.2309_2310delACinsCCAGCGTGGAT - EGFR NM_005228.3:c.2309_2310delACinsCCAGCGTGGAT - EGFR c.2309_2310AC>CCAGCGTGGAT - EGFR c.2309_2310delACinsCCAGCGTGGAT - ERBB c.2309_2310AC>CCAGCGTGGAT - ERBB1 c.2309_2310AC>CCAGCGTGGAT - Epidermal Growth Factor Receptor Gene c.2309_2310AC>CCAGCGTGGAT - HER1 c.2309_2310AC>CCAGCGTGGAT - NM_005228.3:c.2309_2310AC>CCAGCGTGGAT - NM_005228.3:c.2309_2310delACinsCCAGCGTGGAT - NM_005228.3:c.2309_2310delinsCCAGCGTGGAT
/api/v1/systems/nci_thesaurus/nodes/C98620Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.