R13S (p.Arg13Ser) variant of KRT9 (Keratin, type I cytoskeletal 9)
R13S (p.Arg13Ser) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R13S (p.Arg13Ser) variant details
- p.Arg13Ser
- NCI-TCGA Cosmic COSV5585
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available