L108F (p.Leu108Phe) variant of TNFRSF13B (O14836)
L108F (p.Leu108Phe) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
L108F (p.Leu108Phe) variant details
- p.Leu108Phe
- gnomAD rs1214363861
- Missense
- Variant Prioritization Score for Impact Estimate 0.146
- REVEL 0.18
- CADD 1.64
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available