p.Gly66 Ala71del variant of TNFRSF13C (Q96RJ3)
p.Gly66 Ala71del in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and published literature.
p.Gly66 Ala71del variant details
- gnomAD 22-41926254-GCGCC
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.31
- CADD 15.40
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Literature evidence available