W26* (p.Trp26Ter) variant of TNFRSF13B (O14836)
W26* (p.Trp26Ter) in TNFRSF13B (O14836) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
W26* (p.Trp26Ter) variant details
- p.Trp26Ter
- gnomAD rs1193135301
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.53
- CADD 36.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available