S9F (p.Ser9Phe) variant of KRT8 (Keratin, type II cytoskeletal 8)
S9F (p.Ser9Phe) in KRT8 (Keratin, type II cytoskeletal 8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S9F (p.Ser9Phe) variant details
- p.Ser9Phe
- NCI-TCGA Cosmic COSV5317
- cosmic curated COSV53177
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available