V29L (p.Val29Leu) variant of TNFRSF13B (O14836)
V29L (p.Val29Leu) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
V29L (p.Val29Leu) variant details
- p.Val29Leu
- TOPMed rs1409789148
- gnomAD rs1409789148
- Missense
- Variant Prioritization Score for Impact Estimate 0.137
- REVEL 0.19
- CADD 1.53
- PolyPhen-2 0.01
- SIFT 0.11
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available