G38W (p.Gly38Trp) variant of KRT16 (Keratin, type I cytoskeletal 16)
G38W (p.Gly38Trp) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G38W (p.Gly38Trp) variant details
- p.Gly38Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available