S91P (p.Ser91Pro) variant of TNFRSF13B (O14836)
S91P (p.Ser91Pro) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data.
S91P (p.Ser91Pro) variant details
- p.Ser91Pro
- gnomAD rs1331029912
- Missense
- Variant Prioritization Score for Impact Estimate 0.345
- REVEL 0.29
- CADD 15.10
- PolyPhen-2 0.08
- SIFT 0.13
- Most common in the HGDP:YAKUT population (allele frequency 0.04)