S18T (p.Ser18Thr) variant of ABCC2 (Q92887)
S18T (p.Ser18Thr) in ABCC2 (Q92887) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S18T (p.Ser18Thr) variant details
- p.Ser18Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available