R73G (p.Arg73Gly) variant of TNFRSF9 (Q07011)
R73G (p.Arg73Gly) in TNFRSF9 (Q07011) 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 and structural context.
R73G (p.Arg73Gly) variant details
- p.Arg73Gly
- TOPMed rs1248932867
- gnomAD rs1248932867
- Missense
- Variant Prioritization Score for Impact Estimate 0.373
- REVEL 0.38
- CADD 22.60
- PolyPhen-2 0.44
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available