Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.47412464_47412465del | CA022033 | MSH2 | c.696_697del (p.Ser233HisfsTer22) c.498_499del (p.Ser167HisfsTer22) n.768_769del n.758_759del | ClinVar dbSNP |
2 | g.47412465del | CA2499215990 | MSH2 | c.697del (p.Ser233ProfsTer13) c.499del (p.Ser167ProfsTer13) n.769del n.759del | ClinVar dbSNP |