Q57L (p.Gln57Leu) variant of TNFRSF13B (O14836)
Q57L (p.Gln57Leu) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data.
Q57L (p.Gln57Leu) variant details
- p.Gln57Leu
- TOPMed rs1330654104
- Missense
- Variant Prioritization Score for Impact Estimate 0.292
- REVEL 0.31
- CADD 18.10
- PolyPhen-2 0.54
- SIFT 0.03
- Most common in the East Asian population (allele frequency 0.00015)