A28V (p.Ala28Val) variant of TNFRSF1B (P20333)
A28V (p.Ala28Val) in TNFRSF1B (P20333) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
A28V (p.Ala28Val) variant details
- p.Ala28Val
- ESP rs142907823
- Missense
- Variant Prioritization Score for Impact Estimate 0.179
- REVEL 0.19
- MetaLR 0.43
- MetaSVM -0.21
- CADD 0.10
- PolyPhen-2 0.00
- SIFT 0.80
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available