G2A (p.Gly2Ala) variant of TNFRSF9 (Q07011)
G2A (p.Gly2Ala) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
G2A (p.Gly2Ala) variant details
- p.Gly2Ala
- gnomAD rs1486598946
- Missense
- Variant Prioritization Score for Impact Estimate 0.188
- REVEL 0.10
- CADD 13.60
- PolyPhen-2 0.47
- SIFT 0.11
- Most common in the Middle Eastern population (allele frequency 0.00035)
- Structural context available