R26K (p.Arg26Lys) variant of MSH6 (DNA mismatch repair protein Msh6)
R26K (p.Arg26Lys) in MSH6 (DNA mismatch repair protein Msh6) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
R26K (p.Arg26Lys) variant details
- p.Arg26Lys
- TOPMed rs1472227590
- gnomAD rs1472227590
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available