G117R (p.Gly117Arg) variant of SLC37A4 (O43826)
G117R (p.Gly117Arg) in SLC37A4 (O43826) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G117R (p.Gly117Arg) variant details
- p.Gly117Arg
- gnomAD rs1374936577
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available