F97C (p.Phe97Cys) variant of KRT3 (Keratin, type II cytoskeletal 3)
F97C (p.Phe97Cys) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F97C (p.Phe97Cys) variant details
- p.Phe97Cys
- NCI-TCGA Cosmic COSV1005
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available