D37N (p.Asp37Asn) variant of HSPG2 (P98160)
D37N (p.Asp37Asn) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
D37N (p.Asp37Asn) variant details
- p.Asp37Asn
- ExAC rs775580297
- gnomAD rs775580297
- Missense
- REVEL 0.21
- CADD 24.40
- PolyPhen-2 0.95
- SIFT 0.00
- Population evidence available