A59T (p.Ala59Thr) variant of KRT12 (Keratin, type I cytoskeletal 12)
A59T (p.Ala59Thr) in KRT12 (Keratin, type I cytoskeletal 12) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A59T (p.Ala59Thr) variant details
- p.Ala59Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available