| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.47412558C>T | CA10582002 | MSH2 | c.790C>T (p.Gln264Ter) c.592C>T (p.Gln198Ter) n.862C>T n.852C>T | ClinVar dbSNP |
| 2 | g.47412558C>G | CA346732524 | MSH2 | c.790C>G (p.Gln264Glu) c.592C>G (p.Gln198Glu) n.862C>G n.852C>G | dbSNP |