T17R (p.Thr17Arg) variant of TNFRSF13C (Q96RJ3)
T17R (p.Thr17Arg) in TNFRSF13C (Q96RJ3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
T17R (p.Thr17Arg) variant details
- p.Thr17Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.