V38G (p.Val38Gly) variant of KRT6A (Keratin, type II cytoskeletal 6A)
V38G (p.Val38Gly) in KRT6A (Keratin, type II cytoskeletal 6A) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V38G (p.Val38Gly) variant details
- p.Val38Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available