G68G (p.Gly68Gly) variant of TNFRSF13C (Q96RJ3)
G68G (p.Gly68Gly) in TNFRSF13C (Q96RJ3) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and published literature.
G68G (p.Gly68Gly) variant details
- p.Gly68Gly
- rs1330131673
- gnomAD 22-41926264-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.132
- CADD 7.32
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Literature evidence available