S13N (p.Ser13Asn) variant of TNFRSF13B (O14836)
S13N (p.Ser13Asn) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data.
S13N (p.Ser13Asn) variant details
- p.Ser13Asn
- ExAC rs778241634
- gnomAD rs778241634
- Missense
- Variant Prioritization Score for Impact Estimate 0.199
- REVEL 0.15
- CADD 2.93
- PolyPhen-2 0.19
- SIFT 0.56
- Most common in the South Asian population (allele frequency 1.2e-05)