G28R (p.Gly28Arg) variant of TNFRSF13B (O14836)
G28R (p.Gly28Arg) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
G28R (p.Gly28Arg) variant details
- p.Gly28Arg
- gnomAD rs1205656896
- Missense
- Variant Prioritization Score for Impact Estimate 0.355
- REVEL 0.24
- CADD 9.16
- PolyPhen-2 0.06
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available