A9G (p.Ala9Gly) variant of TNFRSF1B (P20333)
A9G (p.Ala9Gly) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data, published literature, and structural context.
A9G (p.Ala9Gly) variant details
- p.Ala9Gly
- gnomAD 1-12167117-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.521
- REVEL 0.35
- MetaLR 0.80
- MetaSVM 0.01
- CADD 24.80
- PolyPhen-2 0.92
- SIFT 0.26
- Population evidence available
- Structural context available
- Literature evidence available