R42W (p.Arg42Trp) variant of TNFRSF13C (Q96RJ3)
R42W (p.Arg42Trp) in TNFRSF13C (Q96RJ3) 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.
R42W (p.Arg42Trp) variant details
- p.Arg42Trp
- gnomAD rs2077634292
- Missense
- Variant Prioritization Score for Impact Estimate 0.363
- REVEL 0.06
- CADD 22.90
- PolyPhen-2 0.66
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)