R49G (p.Arg49Gly) variant of RUNX1 (Q01196)
R49G (p.Arg49Gly) in RUNX1 (Q01196) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
R49G (p.Arg49Gly) variant details
- p.Arg49Gly
- gnomAD rs1487924415
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available