G28* (p.Gly28Ter) variant of IL7R (P16871)
G28* (p.Gly28Ter) in IL7R (P16871) 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 0.87 / 1. The record also includes population frequency data and structural context.
G28* (p.Gly28Ter) variant details
- p.Gly28Ter
- NCI-TCGA Cosmic COSV5740
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.874
- CADD 48.00
- UniProt: Variant assessed as somatic; high impact.
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available