G33R (p.Gly33Arg) variant of TNFRSF4 (P43489)
G33R (p.Gly33Arg) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data.
G33R (p.Gly33Arg) variant details
- p.Gly33Arg
- ExAC rs771136814
- TOPMed rs771136814
- gnomAD rs771136814
- Missense
- Variant Prioritization Score for Impact Estimate 0.385
- REVEL 0.24
- CADD 22.60
- PolyPhen-2 0.93
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 7.2e-05)