G47G (p.Gly47Gly) variant of TNFRSF13C (Q96RJ3)
G47G (p.Gly47Gly) 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.
G47G (p.Gly47Gly) variant details
- p.Gly47Gly
- rs2077630830
- gnomAD 22-41926327-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0979
- CADD 2.44
- Most common in the East Asian population (allele frequency 2.5e-05)
- Literature evidence available