T55M (p.Thr55Met) variant of TNFRSF13C (Q96RJ3)
T55M (p.Thr55Met) 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.
T55M (p.Thr55Met) variant details
- p.Thr55Met
- gnomAD 22-41926304-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- REVEL 0.09
- MetaLR 0.10
- MetaSVM -1.05
- CADD 22.80
- PolyPhen-2 0.76
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Literature evidence available