G66R (p.Gly66Arg) variant of TNFRSF13C (Q96RJ3)
G66R (p.Gly66Arg) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data.
G66R (p.Gly66Arg) variant details
- p.Gly66Arg
- gnomAD rs1402585409
- Missense
- Variant Prioritization Score for Impact Estimate 0.249
- REVEL 0.08
- CADD 22.80
- PolyPhen-2 0.93
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00041)