A101S (p.Ala101Ser) variant of TNFRSF13B (O14836)
A101S (p.Ala101Ser) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
A101S (p.Ala101Ser) variant details
- p.Ala101Ser
- TOPMed rs2087568342
- Missense
- Variant Prioritization Score for Impact Estimate 0.369
- REVEL 0.22
- CADD 5.55
- PolyPhen-2 0.12
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available