C29F (p.Cys29Phe) variant of CDKN1B (P46527)
C29F (p.Cys29Phe) in CDKN1B (P46527) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C29F (p.Cys29Phe) variant details
- p.Cys29Phe
- NCI-TCGA Cosmic COSV9996
- cosmic curated COSV99963
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available