S71T (p.Ser71Thr) variant of HSPG2 (P98160)
S71T (p.Ser71Thr) in HSPG2 (P98160) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance.
S71T (p.Ser71Thr) variant details
- p.Ser71Thr
- TOPMed rs781177979
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance