G47E (p.Gly47Glu) variant of TNFRSF13C (Q96RJ3)
G47E (p.Gly47Glu) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and published literature.
G47E (p.Gly47Glu) variant details
- p.Gly47Glu
- gnomAD 22-41926328-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.107
- REVEL 0.04
- MetaLR 0.04
- MetaSVM -1.02
- CADD 1.59
- PolyPhen-2 0.27
- SIFT 0.41
- Most common in the African/African-American population (allele frequency 0.00012)
- Literature evidence available