| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.47480872G>A | CA020828 | MSH2 | c.2634+1G>A (p.=) c.2436+1G>A (p.=) n.2706+1G>A n.2696+1G>A n.75+1G>A c.*1030+1G>A (p.=) c.*1174+1G>A (p.=) c.*1400+1G>A (p.=) c.*1606+1G>A (p.=) c.*200+1G>A (p.=) | ClinVar dbSNP |
| 2 | g.47480872G>T | CA020831 | MSH2 | c.2634+1G>T (p.=) c.2436+1G>T (p.=) n.2706+1G>T n.2696+1G>T n.75+1G>T c.*1030+1G>T (p.=) c.*1174+1G>T (p.=) c.*1400+1G>T (p.=) c.*1606+1G>T (p.=) c.*200+1G>T (p.=) | ClinVar dbSNP |