R16G (p.Arg16Gly) variant of DCX (O43602)
R16G (p.Arg16Gly) in DCX (O43602) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R16G (p.Arg16Gly) variant details
- p.Arg16Gly
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10057
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available