G69D (p.Gly69Asp) variant of KRT10 (Keratin, type I cytoskeletal 10)
G69D (p.Gly69Asp) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G69D (p.Gly69Asp) variant details
- p.Gly69Asp
- NCI-TCGA Cosmic COSV5409
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.