R3L (p.Arg3Leu) variant of TNFRSF13C (Q96RJ3)
R3L (p.Arg3Leu) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data.
R3L (p.Arg3Leu) variant details
- p.Arg3Leu
- TOPMed rs2077635492
- gnomAD rs2077635492
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- REVEL 0.01
- CADD 8.14
- PolyPhen-2 0.00
- SIFT 0.09
- Most common in the Middle Eastern population (allele frequency 0.0007)