G10D (p.Gly10Asp) variant of TNFRSF13B (O14836)
G10D (p.Gly10Asp) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
G10D (p.Gly10Asp) variant details
- p.Gly10Asp
- ExAC rs746052120
- TOPMed rs746052120
- gnomAD rs746052120
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.34
- CADD 14.00
- PolyPhen-2 0.98
- SIFT 0.50
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available