G47W (p.Gly47Trp) variant of TNFRSF13C (Q96RJ3)
G47W (p.Gly47Trp) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and published literature.
G47W (p.Gly47Trp) variant details
- p.Gly47Trp
- gnomAD 22-41926329-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.189
- REVEL 0.09
- MetaLR 0.08
- MetaSVM -1.01
- CADD 18.60
- PolyPhen-2 0.97
- SIFT 0.04
- Population evidence available
- Literature evidence available