P16L (p.Pro16Leu) variant of TNFRSF13C (Q96RJ3)
P16L (p.Pro16Leu) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data.
P16L (p.Pro16Leu) variant details
- p.Pro16Leu
- ExAC rs774206132
- gnomAD rs774206132
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- REVEL 0.14
- CADD 24.10
- PolyPhen-2 0.83
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)