Y29H (p.Tyr29His) variant of CUL3 (Cullin-3)
Y29H (p.Tyr29His) 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.
Y29H (p.Tyr29His) variant details
- p.Tyr29His
- NCI-TCGA Cosmic COSV5236
- cosmic curated COSV52368
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available