G68V (p.Gly68Val) variant of TNFRSF13C (Q96RJ3)
G68V (p.Gly68Val) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and published literature.
G68V (p.Gly68Val) variant details
- p.Gly68Val
- gnomAD 22-41926265-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0744
- REVEL 0.03
- MetaLR 0.03
- MetaSVM -1.04
- CADD 1.78
- PolyPhen-2 0.01
- SIFT 0.17
- Most common in the HGDP:BURUSHO population (allele frequency 0.042)
- Literature evidence available