G17W (p.Gly17Trp) variant of HSPG2 (P98160)
G17W (p.Gly17Trp) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
G17W (p.Gly17Trp) variant details
- p.Gly17Trp
- Ensembl rs952850076
- Missense
- REVEL 0.18
- CADD 23.30
- PolyPhen-2 0.00
- SIFT 0.02
- Population evidence available