G107C (p.Gly107Cys) variant of KRT2 (P35908)
G107C (p.Gly107Cys) in KRT2 (P35908) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
G107C (p.Gly107Cys) variant details
- p.Gly107Cys
- 1000Genomes rs552494206
- ExAC rs552494206
- gnomAD rs552494206
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available