R29P (p.Arg29Pro) variant of MSH6 (DNA mismatch repair protein Msh6)
R29P (p.Arg29Pro) 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 nonpolyposis colorectal neoplasms. The record also includes structural context.
R29P (p.Arg29Pro) variant details
- p.Arg29Pro
- TOPMed rs1469162224
- gnomAD rs1469162224
- Uncertain significance
- Hereditary nonpolyposis colorectal neoplasms
- Missense
- ClinVar: Uncertain significance (Hereditary nonpolyposis colorectal neoplasms)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available