R59G (p.Arg59Gly) variant of CUL3 (Cullin-3)
R59G (p.Arg59Gly) in CUL3 (Cullin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R59G (p.Arg59Gly) variant details
- p.Arg59Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available