V111F (p.Val111Phe) variant of CDKN1C (P49918)
V111F (p.Val111Phe) in CDKN1C (P49918) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V111F (p.Val111Phe) variant details
- p.Val111Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available