A21G (p.Ala21Gly) variant of HSPG2 (P98160)
A21G (p.Ala21Gly) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
A21G (p.Ala21Gly) variant details
- p.Ala21Gly
- TOPMed rs1381228735
- gnomAD rs1381228735
- Missense
- REVEL 0.07
- CADD 18.90
- PolyPhen-2 0.00
- SIFT 0.36
- Population evidence available