D67A (p.Asp67Ala) variant of HSPG2 (P98160)
D67A (p.Asp67Ala) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
D67A (p.Asp67Ala) variant details
- p.Asp67Ala
- ESP rs370767149
- ExAC rs370767149
- TOPMed rs370767149
- gnomAD rs370767149
- Missense
- REVEL 0.26
- CADD 22.90
- PolyPhen-2 0.06
- SIFT 0.02
- Population evidence available