A2G (p.Ala2Gly) variant of TNFRSF1B (P20333)
A2G (p.Ala2Gly) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data, published literature, and structural context.
A2G (p.Ala2Gly) variant details
- p.Ala2Gly
- gnomAD 1-12167096-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.367
- REVEL 0.25
- MetaLR 0.77
- MetaSVM 0.11
- CADD 23.80
- PolyPhen-2 0.86
- SIFT 0.02
- Population evidence available
- Structural context available
- Literature evidence available