S71G (p.Ser71Gly) variant of KRT17 (Keratin, type I cytoskeletal 17)
S71G (p.Ser71Gly) 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.
S71G (p.Ser71Gly) variant details
- p.Ser71Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available