FGFR3 NM_000142.4:c.742C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 742 of the coding sequence of the FGFR3 gene where cytosine has been mutated to thymine.

**Synonyms:** - CD333 c.742C>T - FGFR3 c.742C>T - Fibroblast Growth Factor Receptor 3 c.742C>T - JTK4 c.742C>T - NM_000142.4:c.742C>T