G66G (p.Gly66Gly) variant of TNFRSF13C (Q96RJ3)
G66G (p.Gly66Gly) in TNFRSF13C (Q96RJ3) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and published literature.
G66G (p.Gly66Gly) variant details
- p.Gly66Gly
- gnomAD 22-41926270-C-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.103
- CADD 3.09
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Literature evidence available