R2G (p.Arg2Gly) variant of RUNX1 (Q01196)
R2G (p.Arg2Gly) in RUNX1 (Q01196) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
R2G (p.Arg2Gly) variant details
- p.Arg2Gly
- gnomAD rs1472759880
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available