CHD6 NM_032221.5:c.4800C>G

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 4800 of the coding sequence of the CHD6 gene where cytosine has been mutated to guanine.

**Synonyms:** - CHD-6 c.4800C>G - CHD6 c.4800C>G - Chromodomain Helicase DNA Binding Protein 6 c.4800C>G - NM_032221.5:c.4800C>G - RIGB c.4800C>G - Radiation-Induced Gene B c.4800C>G