P17S (p.Pro17Ser) variant of GABRG2 (P18507)
P17S (p.Pro17Ser) in GABRG2 (P18507) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P17S (p.Pro17Ser) variant details
- p.Pro17Ser
- TOPMed rs1429217294
- gnomAD rs1429217294
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available