S21Y (p.Ser21Tyr) variant of SLC2A2 (P11168)
S21Y (p.Ser21Tyr) in SLC2A2 (P11168) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S21Y (p.Ser21Tyr) variant details
- p.Ser21Tyr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available