R55H (p.Arg55His) variant of TNFRSF4 (P43489)
R55H (p.Arg55His) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data.
R55H (p.Arg55His) variant details
- p.Arg55His
- ExAC rs745731727
- TOPMed rs745731727
- gnomAD rs745731727
- Missense
- Variant Prioritization Score for Impact Estimate 0.629
- REVEL 0.53
- CADD 25.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 2.4e-05)