S8T (p.Ser8Thr) variant of PMS2 (P54278)
S8T (p.Ser8Thr) in PMS2 (P54278) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes published literature and structural context.
S8T (p.Ser8Thr) variant details
- p.Ser8Thr
- rs1352544158
- ClinGen CA366745219
- ClinVar RCV000772979
- TOPMed rs1352544158
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.49
- AlphaMissense 0.08
- MetaLR 0.54
- MetaSVM -0.04
- PolyPhen-2 0.84
- SIFT 0.19
- MutPred 0.21
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)