R17G (p.Arg17Gly) variant of POLD1 (P28340)
R17G (p.Arg17Gly) in POLD1 (P28340) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
R17G (p.Arg17Gly) variant details
- p.Arg17Gly
- 1000Genomes rs570461545
- ExAC rs570461545
- TOPMed rs570461545
- gnomAD rs570461545
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available