S39* (p.Ser39Ter) variant of IL7R (P16871)
S39* (p.Ser39Ter) in IL7R (P16871) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S39* (p.Ser39Ter) variant details
- p.Ser39Ter
- NCI-TCGA TCGA novel
- Ensembl rs1759787685
- Variant assessed as somatic; high impact.
- Stop Gained
- UniProt: Variant assessed as somatic; high impact.
- Structural context available