Y118C (p.Tyr118Cys) variant of KRT13 (Keratin, type I cytoskeletal 13)
Y118C (p.Tyr118Cys) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in WSN2. The record also includes structural context.
Y118C (p.Tyr118Cys) variant details
- p.Tyr118Cys
- NCI-TCGA Cosmic COSV9987
- cosmic curated COSV99877
- Variant assessed as somatic; moderate impact.
- in WSN2
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in WSN2)
- Structural context available