W40* (p.Trp40Ter) variant of TNFRSF13B (O14836)
W40* (p.Trp40Ter) in TNFRSF13B (O14836) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.85 / 1. The record also includes population frequency data and structural context.
W40* (p.Trp40Ter) variant details
- p.Trp40Ter
- ExAC rs759576194
- gnomAD rs759576194
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.846
- CADD 36.00
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available