V119G (p.Val119Gly) variant of TNFRSF1A (P19438)
V119G (p.Val119Gly) in TNFRSF1A (P19438) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
V119G (p.Val119Gly) variant details
- p.Val119Gly
- ExAC rs772756388
- gnomAD rs772756388
- Missense
- Variant Prioritization Score for Impact Estimate 0.419
- REVEL 0.48
- CADD 23.60
- PolyPhen-2 0.55
- SIFT 0.00
- Most common in the South Asian population (allele frequency 7e-05)
- Structural context available