C29R (p.Cys29Arg) variant of CDKN1B (P46527)
C29R (p.Cys29Arg) in CDKN1B (P46527) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
C29R (p.Cys29Arg) variant details
- p.Cys29Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available