G38V (p.Gly38Val) variant of SLC22A1 (O15245)
G38V (p.Gly38Val) in SLC22A1 (O15245) is a missense change. The record also includes population frequency data and structural context.
G38V (p.Gly38Val) variant details
- p.Gly38Val
- 1000Genomes rs35888596
- ESP rs35888596
- ExAC rs35888596
- TOPMed rs35888596
- Missense
- Population evidence available
- Structural context available