D80G (p.Asp80Gly) variant of TNFRSF13B (O14836)
D80G (p.Asp80Gly) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data.
D80G (p.Asp80Gly) variant details
- p.Asp80Gly
- 1000Genomes rs546335485
- Missense
- Variant Prioritization Score for Impact Estimate 0.743
- REVEL 0.82
- CADD 25.40
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)