G17V (p.Gly17Val) variant of HSPG2 (P98160)
G17V (p.Gly17Val) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
G17V (p.Gly17Val) variant details
- p.Gly17Val
- Ensembl rs1644512136
- Missense
- REVEL 0.16
- CADD 15.30
- PolyPhen-2 0.09
- SIFT 0.17
- Population evidence available