A15V (p.Ala15Val) variant of TNFRSF4 (P43489)
A15V (p.Ala15Val) in TNFRSF4 (P43489) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data.
A15V (p.Ala15Val) variant details
- p.Ala15Val
- ExAC rs754807989
- TOPMed rs754807989
- gnomAD rs754807989
- Missense
- Variant Prioritization Score for Impact Estimate 0.464
- REVEL 0.25
- CADD 21.20
- PolyPhen-2 0.99
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)