Q17* (p.Gln17Ter) variant of TNFRSF13B (O14836)
Q17* (p.Gln17Ter) in TNFRSF13B (O14836) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data.
Q17* (p.Gln17Ter) variant details
- p.Gln17Ter
- rs764951604
- NCI-TCGA Cosmic COSV5542
- cosmic curated COSV55428
- ExAC rs764951604
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.454
- CADD 35.00
- UniProt: Variant assessed as somatic; high impact.
- Most common in the REMAINING population (allele frequency 1.7e-05)