Q59R (p.Gln59Arg) variant of TNFRSF9 (Q07011)
Q59R (p.Gln59Arg) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
Q59R (p.Gln59Arg) variant details
- p.Gln59Arg
- ExAC rs758956577
- gnomAD rs758956577
- Missense
- Variant Prioritization Score for Impact Estimate 0.468
- REVEL 0.41
- CADD 23.00
- PolyPhen-2 0.94
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 9.9e-06)
- Structural context available