D19G (p.Asp19Gly) variant of MSH6 (DNA mismatch repair protein Msh6)
D19G (p.Asp19Gly) in MSH6 (DNA mismatch repair protein Msh6) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
D19G (p.Asp19Gly) variant details
- p.Asp19Gly
- rs1553408133
- ClinGen CA346734560
- ClinVar RCV000528902
- TOPMed rs1553408133
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available