R9Q (p.Arg9Gln) variant of TNFRSF13C (Q96RJ3)
R9Q (p.Arg9Gln) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data.
R9Q (p.Arg9Gln) variant details
- p.Arg9Gln
- TOPMed rs2077635183
- gnomAD rs2077635183
- Missense
- Variant Prioritization Score for Impact Estimate 0.137
- REVEL 0.05
- CADD 14.20
- PolyPhen-2 0.27
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)