R66G (p.Arg66Gly) variant of TNFRSF9 (Q07011)
R66G (p.Arg66Gly) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
R66G (p.Arg66Gly) variant details
- p.Arg66Gly
- 1000Genomes rs567725192
- ExAC rs567725192
- gnomAD rs567725192
- Missense
- Variant Prioritization Score for Impact Estimate 0.464
- REVEL 0.46
- CADD 22.20
- PolyPhen-2 0.25
- SIFT 0.00
- Most common in the 1KG:IBS population (allele frequency 0.0048)
- Structural context available