C98698Level 8
EGFR NM_005228.3:c.2316_2321dup
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A complex nucleotide substitution where the deletion of guanine at position 2322 is followed by the insertion of seven nucleotides, cytosine-cytosine-adenine-cytosine-guanine-thymine-guanine, into the coding sequence of the EGFR gene.
**Synonyms:** - EGFR NM_005228.3:c.2322delGinsCCACGTG - EGFR NM_005228.3:c.2322delGinsCCACGTG - EGFR c.2322_2322G>CCACGTG - EGFR c.delGinsCCACGTG - ERBB c.2322_2322G>CCACGTG - ERBB1 c.2322_2322G>CCACGTG - Epidermal Growth Factor Receptor Gene c.2322_2322G>CCACGTG - HER1 c.2322_2322G>CCACGTG - NM_005228.3:c.2316_2321dup - NM_005228.3:c.2322_2322G>CCACGTG - NM_005228.3:c.2322delGinsCCACGTG
GET
/api/v1/systems/nci_thesaurus/nodes/C98698Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.