R99A (p.Arg99Ala) variant of CDKN1C (P49918)
R99A (p.Arg99Ala) in CDKN1C (P49918) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
R99A (p.Arg99Ala) variant details
- p.Arg99Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available