A30S (p.Ala30Ser) variant of TNFRSF13B (O14836)
A30S (p.Ala30Ser) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
A30S (p.Ala30Ser) variant details
- p.Ala30Ser
- TOPMed rs1400914097
- gnomAD rs1400914097
- Missense
- Variant Prioritization Score for Impact Estimate 0.358
- REVEL 0.40
- CADD 17.70
- PolyPhen-2 0.62
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available