Y69F (p.Tyr69Phe) variant of KRT14 (Keratin, type I cytoskeletal 14)
Y69F (p.Tyr69Phe) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Y69F (p.Tyr69Phe) variant details
- p.Tyr69Phe
- NCI-TCGA Cosmic COSV5142
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available