G23V (p.Gly23Val) variant of CDKN1A (P38936)
G23V (p.Gly23Val) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G23V (p.Gly23Val) variant details
- p.Gly23Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.