H16Y (p.His16Tyr) variant of HSPG2 (P98160)
H16Y (p.His16Tyr) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
H16Y (p.His16Tyr) variant details
- p.His16Tyr
- TOPMed rs1644512344
- gnomAD rs1644512344
- Missense
- REVEL 0.20
- CADD 15.70
- PolyPhen-2 0.03
- SIFT 1.00
- Population evidence available