E139V (p.Glu139Val) variant of HSPG2 (P98160)
E139V (p.Glu139Val) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
E139V (p.Glu139Val) variant details
- p.Glu139Val
- gnomAD rs1387834822
- Missense
- REVEL 0.25
- CADD 24.30
- PolyPhen-2 0.04
- SIFT 0.04
- Population evidence available