DRD2 NM_000795.3:c.-486_-485insC

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide insertion of a cytosine between positions -486 and -485 in the 5' promoter region of the DRD2 gene.

**Synonyms:** - DRD2 -141 indel - DRD2 -141C Ins/Del - DRD2 -141insC Mutation - DRD2 c.-486_-485insC - Dopamine Receptor D2 c.-486_-485insC - NM_000795.3:c.-486_-485insC