G24D (p.Gly24Asp) variant of TNFRSF13B (O14836)
G24D (p.Gly24Asp) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
G24D (p.Gly24Asp) variant details
- p.Gly24Asp
- gnomAD rs1156339689
- Missense
- Variant Prioritization Score for Impact Estimate 0.377
- REVEL 0.40
- CADD 16.10
- PolyPhen-2 0.02
- SIFT 0.07
- Most common in the 1KG:MXL population (allele frequency 0.0081)
- Structural context available