V119A (p.Val119Ala) variant of TNFRSF1A (P19438)
V119A (p.Val119Ala) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
V119A (p.Val119Ala) variant details
- p.Val119Ala
- ExAC rs772756388
- gnomAD rs772756388
- Missense
- Variant Prioritization Score for Impact Estimate 0.336
- REVEL 0.41
- CADD 14.20
- PolyPhen-2 0.04
- SIFT 0.19
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available