A11G (p.Ala11Gly) variant of TNFRSF1B (P20333)
A11G (p.Ala11Gly) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
A11G (p.Ala11Gly) variant details
- p.Ala11Gly
- gnomAD 1-12167123-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.319
- REVEL 0.27
- MetaLR 0.60
- MetaSVM -0.42
- CADD 21.60
- PolyPhen-2 0.00
- SIFT 0.12
- Population evidence available
- Structural context available
- Literature evidence available