D56G (p.Asp56Gly) variant of HSPG2 (P98160)
D56G (p.Asp56Gly) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
D56G (p.Asp56Gly) variant details
- p.Asp56Gly
- Ensembl rs1642735834
- Missense
- REVEL 0.38
- CADD 25.30
- PolyPhen-2 0.93
- SIFT 0.00
- Population evidence available