Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|

2 | g.47429740A>G | CA017174 | MSH2 | c.1077-2A>G (p.=) c.879-2A>G (p.=) c.*49-2A>G (p.=) n.1149-2A>G | ClinVar dbSNP |

2 | g.47429740A>T | CA017180 | MSH2 | c.1077-2A>T (p.=) c.879-2A>T (p.=) c.*49-2A>T (p.=) n.1149-2A>T | ClinVar dbSNP |

2 | g.47429740A>C | CA017167 | MSH2 | c.1077-2A>C (p.=) c.879-2A>C (p.=) c.*49-2A>C (p.=) n.1149-2A>C | ClinVar dbSNP |