P59L (p.Pro59Leu) variant of TNFRSF13C (Q96RJ3)
P59L (p.Pro59Leu) 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.
P59L (p.Pro59Leu) variant details
- p.Pro59Leu
- TOPMed rs899866976
- gnomAD rs899866976
- Missense
- Variant Prioritization Score for Impact Estimate 0.226
- REVEL 0.13
- CADD 20.30
- PolyPhen-2 0.03
- SIFT 0.00
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)