A78G (p.Ala78Gly) variant of KRT6B (Keratin, type II cytoskeletal 6B)
A78G (p.Ala78Gly) in KRT6B (Keratin, type II cytoskeletal 6B) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A78G (p.Ala78Gly) variant details
- p.Ala78Gly
- NCI-TCGA Cosmic COSV9936
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available