S52G (p.Ser52Gly) variant of TNFRSF9 (Q07011)
S52G (p.Ser52Gly) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
S52G (p.Ser52Gly) variant details
- p.Ser52Gly
- ExAC rs774925474
- gnomAD rs774925474
- Missense
- Variant Prioritization Score for Impact Estimate 0.392
- REVEL 0.29
- CADD 23.70
- PolyPhen-2 0.78
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available