G68V (p.Gly68Val) variant of KRT17 (Keratin, type I cytoskeletal 17)
G68V (p.Gly68Val) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G68V (p.Gly68Val) variant details
- p.Gly68Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available