I92V (p.Ile92Val) variant of TNFRSF13B (O14836)
I92V (p.Ile92Val) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data.
I92V (p.Ile92Val) variant details
- p.Ile92Val
- gnomAD rs1322152086
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- REVEL 0.16
- CADD 16.30
- PolyPhen-2 0.17
- SIFT 0.18
- Most common in the HGDP:FRENCH population (allele frequency 0.019)