R41Q (p.Arg41Gln) variant of TNFRSF4 (P43489)
R41Q (p.Arg41Gln) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
R41Q (p.Arg41Gln) variant details
- p.Arg41Gln
- ExAC rs779828255
- TOPMed rs779828255
- gnomAD rs779828255
- Missense
- Variant Prioritization Score for Impact Estimate 0.226
- REVEL 0.32
- CADD 5.42
- PolyPhen-2 0.28
- SIFT 0.02
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available