R47L (p.Arg47Leu) variant of HSPG2 (P98160)
R47L (p.Arg47Leu) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
R47L (p.Arg47Leu) variant details
- p.Arg47Leu
- ExAC rs751202082
- TOPMed rs751202082
- gnomAD rs751202082
- Missense
- REVEL 0.05
- CADD 15.90
- PolyPhen-2 0.00
- SIFT 0.24
- Population evidence available