| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.47414347del | CA16617566 | MSH2 | c.871del (p.Leu291Ter) c.673del (p.Leu225Ter) n.943del n.933del | ClinVar dbSNP |
| 2 | g.47414347C= | CA2495833990 | MSH2 | c.871C= (p.Leu291=) c.673C= (p.Leu225=) n.943C= n.933C= | dbSNP dbSNP |