EGFR NM_005228.5:c.2318A>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 2318 of the coding sequence of the EGFR gene where adenine has been mutated to thymine.

**Synonyms:** - EGFR c.2318A>T - ERBB c.2318A>T - ERBB1 c.2318A>T - Epidermal Growth Factor Receptor Gene c.2318A>T - HER1 c.2318A>T - NM_005228.5:c.2318A>T