A101E (p.Ala101Glu) variant of TNFRSF13B (O14836)
A101E (p.Ala101Glu) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
A101E (p.Ala101Glu) variant details
- p.Ala101Glu
- TOPMed rs1310977376
- gnomAD rs1310977376
- Missense
- Variant Prioritization Score for Impact Estimate 0.254
- REVEL 0.26
- CADD 13.20
- PolyPhen-2 0.04
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available