P59Q (p.Pro59Gln) variant of TNFRSF13C (Q96RJ3)
P59Q (p.Pro59Gln) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data.
P59Q (p.Pro59Gln) variant details
- p.Pro59Gln
- TOPMed rs899866976
- gnomAD rs899866976
- Missense
- Variant Prioritization Score for Impact Estimate 0.234
- REVEL 0.11
- CADD 22.90
- PolyPhen-2 0.93
- SIFT 0.00
- Most common in the 1KG:MSL population (allele frequency 0.013)