S78G (p.Ser78Gly) variant of KRT14 (Keratin, type I cytoskeletal 14)
S78G (p.Ser78Gly) 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.
S78G (p.Ser78Gly) variant details
- p.Ser78Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available