G78E (p.Gly78Glu) variant of KRT2 (P35908)
G78E (p.Gly78Glu) in KRT2 (P35908) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G78E (p.Gly78Glu) variant details
- p.Gly78Glu
- NCI-TCGA Cosmic COSV5901
- Ensembl rs1941258636
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available