S39I (p.Ser39Ile) variant of KRT1 (Keratin, type II cytoskeletal 1)
S39I (p.Ser39Ile) in KRT1 (Keratin, type II cytoskeletal 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S39I (p.Ser39Ile) variant details
- p.Ser39Ile
- NCI-TCGA Cosmic COSV5286
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available