D68G (p.Asp68Gly) variant of XPC (Q01831)
D68G (p.Asp68Gly) in XPC (Q01831) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes population frequency data and structural context.
D68G (p.Asp68Gly) variant details
- p.Asp68Gly
- 1000Genomes rs56012223
- ExAC rs56012223
- TOPMed rs56012223
- gnomAD rs56012223
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Population evidence available
- Structural context available