G41D (p.Gly41Asp) variant of KRT18 (Keratin, type I cytoskeletal 18)
G41D (p.Gly41Asp) in KRT18 (Keratin, type I cytoskeletal 18) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G41D (p.Gly41Asp) variant details
- p.Gly41Asp
- NCI-TCGA Cosmic COSV1011
- cosmic curated COSV10118
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available