D56N (p.Asp56Asn) variant of HSPG2 (P98160)
D56N (p.Asp56Asn) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
D56N (p.Asp56Asn) variant details
- p.Asp56Asn
- Ensembl rs2152773281
- Missense
- REVEL 0.24
- CADD 24.80
- Population evidence available