G98R (p.Gly98Arg) variant of TNFRSF9 (Q07011)
G98R (p.Gly98Arg) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and structural context.
G98R (p.Gly98Arg) variant details
- p.Gly98Arg
- gnomAD rs1330172090
- Missense
- Variant Prioritization Score for Impact Estimate 0.0659
- REVEL 0.03
- CADD 8.72
- PolyPhen-2 0.13
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available