S62W (p.Ser62Trp) variant of TNFRSF13C (Q96RJ3)
S62W (p.Ser62Trp) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data.
S62W (p.Ser62Trp) variant details
- p.Ser62Trp
- gnomAD rs1281840629
- Missense
- Variant Prioritization Score for Impact Estimate 0.391
- REVEL 0.16
- CADD 25.40
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the HGDP:FRENCH population (allele frequency 0.019)