P42H (p.Pro42His) variant of TNFRSF13B (O14836)
P42H (p.Pro42His) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data.
P42H (p.Pro42His) variant details
- p.Pro42His
- ExAC rs770198071
- gnomAD rs770198071
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.27
- CADD 14.50
- PolyPhen-2 0.84
- SIFT 0.17
- Most common in the East Asian population (allele frequency 0.00015)