M46T (p.Met46Thr) variant of HSPG2 (P98160)
M46T (p.Met46Thr) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
M46T (p.Met46Thr) variant details
- p.Met46Thr
- ExAC rs769789769
- TOPMed rs769789769
- gnomAD rs769789769
- Missense
- REVEL 0.02
- CADD 3.06
- PolyPhen-2 0.00
- SIFT 0.31
- Population evidence available