P59T (p.Pro59Thr) variant of TNFRSF13C (Q96RJ3)
P59T (p.Pro59Thr) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and published literature.
P59T (p.Pro59Thr) variant details
- p.Pro59Thr
- gnomAD 22-41926293-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.3
- REVEL 0.12
- MetaLR 0.11
- MetaSVM -0.89
- CADD 22.80
- PolyPhen-2 0.61
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Literature evidence available