G13R (p.Gly13Arg) variant of TNFRSF1B (P20333)
G13R (p.Gly13Arg) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data, published literature, and structural context.
G13R (p.Gly13Arg) variant details
- p.Gly13Arg
- gnomAD 1-12167128-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.547
- REVEL 0.53
- MetaLR 0.78
- MetaSVM 0.08
- CADD 27.30
- PolyPhen-2 0.77
- SIFT 0.07
- Population evidence available
- Structural context available
- Literature evidence available