Q23R (p.Gln23Arg) variant of TNFRSF13B (O14836)
Q23R (p.Gln23Arg) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data.
Q23R (p.Gln23Arg) variant details
- p.Gln23Arg
- gnomAD rs1409221013
- Missense
- Variant Prioritization Score for Impact Estimate 0.454
- REVEL 0.40
- CADD 24.10
- PolyPhen-2 0.97
- SIFT 0.10
- Most common in the REMAINING population (allele frequency 1.7e-05)