A17P (p.Ala17Pro) variant of CDKN1A (P38936)
A17P (p.Ala17Pro) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
A17P (p.Ala17Pro) variant details
- p.Ala17Pro
- Ensembl rs2150312837
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.