EGFR NM_005228.5:c.1787C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1787 of the coding sequence of the EGFR gene where cytosine has been mutated to thymine.

**Synonyms:** - EGFR c.1787C>T - ERBB c.1787C>T - ERBB1 c.1787C>T - Epidermal Growth Factor Receptor Gene c.1787C>T - HER1 c.1787C>T - NM_005228.5:c.1787C>T