A41G (p.Ala41Gly) variant of RUNX1 (Q01196)
A41G (p.Ala41Gly) in RUNX1 (Q01196) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A41G (p.Ala41Gly) variant details
- p.Ala41Gly
- NCI-TCGA Cosmic COSV5589
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available