G32V (p.Gly32Val) variant of MSH6 (DNA mismatch repair protein Msh6)
G32V (p.Gly32Val) 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.
G32V (p.Gly32Val) variant details
- p.Gly32Val
- rs771426932
- ClinGen CA16617617
- ClinVar RCV000487312
- ClinVar RCV000566154
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- 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)