V77G (p.Val77Gly) variant of KRT8 (Keratin, type II cytoskeletal 8)
V77G (p.Val77Gly) in KRT8 (Keratin, type II cytoskeletal 8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V77G (p.Val77Gly) variant details
- p.Val77Gly
- NCI-TCGA Cosmic COSV5317
- cosmic curated COSV53179
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available