T13N (p.Thr13Asn) variant of SLC2A2 (P11168)
T13N (p.Thr13Asn) in SLC2A2 (P11168) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
T13N (p.Thr13Asn) variant details
- p.Thr13Asn
- gnomAD rs1247912820
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available