K13M (p.Lys13Met) variant of MSH6 (DNA mismatch repair protein Msh6)
K13M (p.Lys13Met) in MSH6 (DNA mismatch repair protein Msh6) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes published literature and structural context.
K13M (p.Lys13Met) variant details
- p.Lys13Met
- rs41294988
- ClinGen CA346734528
- ClinVar RCV000525094
- ClinVar RCV000567533
- Likely benign
- Missense
- EBI: Likely benign (in dbSNP:rs41294988)
- UniProt: Likely benign (in dbSNP:rs41294988)
- 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)