Y85C (p.Tyr85Cys) variant of FLG (Filaggrin)
Y85C (p.Tyr85Cys) in FLG (Filaggrin) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes population frequency data.
Y85C (p.Tyr85Cys) variant details
- p.Tyr85Cys
- ExAC rs755737937
- TOPMed rs755737937
- gnomAD rs755737937
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Population evidence available