L52F (p.Leu52Phe) variant of CUL3 (Cullin-3)
L52F (p.Leu52Phe) 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.
L52F (p.Leu52Phe) variant details
- p.Leu52Phe
- NCI-TCGA Cosmic COSV5236
- Ensembl rs2106304711
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available