S2A (p.Ser2Ala) variant of CDKN1A (P38936)
S2A (p.Ser2Ala) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S2A (p.Ser2Ala) variant details
- p.Ser2Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.