S89P (p.Ser89Pro) variant of SLC2A4 (P14672)
S89P (p.Ser89Pro) in SLC2A4 (P14672) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S89P (p.Ser89Pro) variant details
- p.Ser89Pro
- rs1167739117
- TOPMed rs1167739117
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available