S18F (p.Ser18Phe) variant of KRT12 (Keratin, type I cytoskeletal 12)
S18F (p.Ser18Phe) in KRT12 (Keratin, type I cytoskeletal 12) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S18F (p.Ser18Phe) variant details
- p.Ser18Phe
- rs971553130
- TOPMed rs971553130
- NCI-TCGA Cosmic COSV9928
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available