E110D (p.Glu110Asp) variant of HSPG2 (P98160)
E110D (p.Glu110Asp) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
E110D (p.Glu110Asp) variant details
- p.Glu110Asp
- Ensembl rs1642289325
- Missense
- REVEL 0.16
- CADD 17.00
- PolyPhen-2 0.00
- SIFT 0.09
- Population evidence available