T42A (p.Thr42Ala) variant of HSPG2 (P98160)
T42A (p.Thr42Ala) in HSPG2 (P98160) is a missense change. The record also includes variant effect predictions and population frequency data.
T42A (p.Thr42Ala) variant details
- p.Thr42Ala
- Ensembl rs1642739349
- Missense
- REVEL 0.07
- CADD 0.63
- PolyPhen-2 0.00
- SIFT 0.30
- Population evidence available