Q17E (p.Gln17Glu) variant of TNFRSF13B (O14836)
Q17E (p.Gln17Glu) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data.
Q17E (p.Gln17Glu) variant details
- p.Gln17Glu
- ExAC rs764951604
- gnomAD rs764951604
- Missense
- Variant Prioritization Score for Impact Estimate 0.2
- REVEL 0.18
- CADD 3.52
- PolyPhen-2 0.02
- SIFT 1.00
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)