G16C (p.Gly16Cys) variant of KRT1 (Keratin, type II cytoskeletal 1)
G16C (p.Gly16Cys) 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.
G16C (p.Gly16Cys) variant details
- p.Gly16Cys
- NCI-TCGA Cosmic COSV5286
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available