S28F (p.Ser28Phe) variant of KRT17 (Keratin, type I cytoskeletal 17)
S28F (p.Ser28Phe) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S28F (p.Ser28Phe) variant details
- p.Ser28Phe
- NCI-TCGA Cosmic COSV6086
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available