E37G (p.Glu37Gly) variant of TNFRSF13B (O14836)
E37G (p.Glu37Gly) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
E37G (p.Glu37Gly) variant details
- p.Glu37Gly
- 1000Genomes rs2143662592
- Missense
- Variant Prioritization Score for Impact Estimate 0.563
- REVEL 0.61
- CADD 27.60
- PolyPhen-2 1.00
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available