A56T (p.Ala56Thr) variant of TNFRSF13C (Q96RJ3)
A56T (p.Ala56Thr) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and published literature.
A56T (p.Ala56Thr) variant details
- p.Ala56Thr
- gnomAD 22-41926302-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.243
- REVEL 0.05
- MetaLR 0.05
- MetaSVM -1.08
- CADD 22.50
- PolyPhen-2 0.46
- SIFT 0.04
- Most common in the REMAINING population (allele frequency 0.00048)
- Literature evidence available