| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.47414335G>T | CA022437 | MSH2 | c.859G>T (p.Gly287Ter) c.661G>T (p.Gly221Ter) n.931G>T n.921G>T | ClinVar dbSNP |
| 2 | g.47414335G>C | CA346732855 | MSH2 | c.859G>C (p.Gly287Arg) c.661G>C (p.Gly221Arg) n.931G>C n.921G>C | ClinVar dbSNP |
| 2 | g.47414335G>A | CA346732856 | MSH2 | c.859G>A (p.Gly287Arg) c.661G>A (p.Gly221Arg) n.931G>A n.921G>A | ClinVar dbSNP |