N39M (p.Asn39Met) variant of CUL3 (Cullin-3)
N39M (p.Asn39Met) in CUL3 (Cullin-3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
N39M (p.Asn39Met) variant details
- p.Asn39Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available