W7G (p.Trp7Gly) variant of TNFRSF1B (P20333)
W7G (p.Trp7Gly) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
W7G (p.Trp7Gly) variant details
- p.Trp7Gly
- gnomAD 1-12167110-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.582
- REVEL 0.59
- MetaLR 0.87
- MetaSVM 0.32
- CADD 27.70
- PolyPhen-2 0.99
- SIFT 0.05
- Population evidence available
- Structural context available
- Literature evidence available