P97S (p.Pro97Ser) variant of TNFRSF13B (O14836)
P97S (p.Pro97Ser) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data.
P97S (p.Pro97Ser) variant details
- p.Pro97Ser
- ExAC rs757279559
- gnomAD rs757279559
- Missense
- Variant Prioritization Score for Impact Estimate 0.671
- REVEL 0.68
- CADD 24.00
- PolyPhen-2 1.00
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 0.00041)