V137I (p.Val137Ile) variant of SLC2A2 (P11168)
V137I (p.Val137Ile) in SLC2A2 (P11168) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V137I (p.Val137Ile) variant details
- p.Val137Ile
- ESP rs144125084
- ExAC rs144125084
- TOPMed rs144125084
- gnomAD rs144125084
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available