S9T (p.Ser9Thr) variant of MSH6 (DNA mismatch repair protein Msh6)
S9T (p.Ser9Thr) 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 published literature and structural context.
S9T (p.Ser9Thr) variant details
- p.Ser9Thr
- rs1572697767
- ClinGen CA346734507
- ClinVar RCV001016350
- Ensembl rs1572697767
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)