S27K (p.Ser27Lys) variant of CDKN1A (P38936)
S27K (p.Ser27Lys) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S27K (p.Ser27Lys) variant details
- p.Ser27Lys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available