T9S (p.Thr9Ser) variant of PMS2 (P54278)
T9S (p.Thr9Ser) in PMS2 (P54278) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
T9S (p.Thr9Ser) variant details
- p.Thr9Ser
- TOPMed rs786202383
- gnomAD rs786202383
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available