| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.47410322T>C | CA021524 | MSH2 | c.595T>C (p.Cys199Arg) c.397T>C (p.Cys133Arg) n.667T>C n.657T>C | ClinVar dbSNP COSMIC |
| 2 | g.47410322T>G | CA346731038 | MSH2 | c.595T>G (p.Cys199Gly) c.397T>G (p.Cys133Gly) n.667T>G n.657T>G | ClinVar dbSNP |
| 2 | g.47410322T= | CA2495831314 | MSH2 | c.595T= (p.Cys199=) c.397T= (p.Cys133=) n.667T= n.657T= | dbSNP |