V9L (p.Val9Leu) variant of TNFRSF9 (Q07011)
V9L (p.Val9Leu) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
V9L (p.Val9Leu) variant details
- p.Val9Leu
- ExAC rs76908749
- gnomAD rs76908749
- Missense
- Variant Prioritization Score for Impact Estimate 0.0511
- REVEL 0.01
- CADD 5.42
- PolyPhen-2 0.01
- SIFT 0.11
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.5e-05)
- Structural context available