K16G (p.Lys16Gly) variant of CDKN1A (P38936)
K16G (p.Lys16Gly) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
K16G (p.Lys16Gly) variant details
- p.Lys16Gly
- NCI-TCGA Cosmic COSV5518
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.