C98539Level 8
EGFR NM_005228.3:c.2236_2250del15
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A deletion of 15 nucleotides from the coding sequence of the EGFR gene from position 2236 through 2250.
**Synonyms:** - EGFR E746-A750 Gene Mutation - EGFR c.2236_2250del15 - ERBB c.2236_2250del15 - ERBB1 c.2236_2250del15 - Epidermal Growth Factor Receptor Gene c.2236_2250del15 - HER1 c.2236_2250del15 - NM_005228.3:c.2236_2250 - NM_005228.3:c.2236_2250del - NM_005228.3:c.2236_2250del15
GET
/api/v1/systems/nci_thesaurus/nodes/C98539Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.