G37T (p.Gly37Thr) variant of SMC3 (Q9UQE7)
G37T (p.Gly37Thr) in SMC3 (Q9UQE7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G37T (p.Gly37Thr) variant details
- p.Gly37Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available