P22S (p.Pro22Ser) variant of TNFRSF13B (O14836)
P22S (p.Pro22Ser) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data.
P22S (p.Pro22Ser) variant details
- p.Pro22Ser
- TOPMed rs1221013886
- Missense
- Variant Prioritization Score for Impact Estimate 0.445
- REVEL 0.45
- CADD 22.30
- PolyPhen-2 0.81
- SIFT 0.08
- Most common in the 1KG:MXL population (allele frequency 0.0081)