C98612Level 8
EGFR NM_005228.3:c.2290_2291ins12
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** An insertion of 12 nucleotides, TCCAGGAAGCCT, between position 2302 and 2303 of the coding sequence of the EGFR gene.
**Synonyms:** - EGFR NM_005228.3:c.2302_2303insTCCAGGAAGCCT - EGFR c.2290_2291ins12 - EGFR c.2302_2303insTCCAGGAAGCCT - ERBB c.2290_2291ins12 - ERBB1 c.2290_2291ins12 - Epidermal Growth Factor Receptor Gene c.2290_2291ins12 - HER1 c.2290_2291ins12 - NM_005228.3:c.2290_2291ins12 - NM_005228.3:c.2302_2303insTCCAGGAAGCCT
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/api/v1/systems/nci_thesaurus/nodes/C98612Hierarchy Explorer
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Cross-system equivalences0
No cross-system equivalences mapped for this node.