W17R (p.Trp17Arg) variant of TNFRSF1B (P20333)
W17R (p.Trp17Arg) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
W17R (p.Trp17Arg) variant details
- p.Trp17Arg
- TOPMed rs1464781369
- Missense
- Variant Prioritization Score for Impact Estimate 0.513
- REVEL 0.52
- MetaLR 0.76
- MetaSVM -0.06
- CADD 26.00
- PolyPhen-2 0.72
- SIFT 0.03
- Population evidence available
- Structural context available