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

9 | g.116865979C>T | CA199061069 | ASTN2 | c.1737-2246G>A (p.=) c.1890-2246G>A (p.=) c.1878-2246G>A (p.=) c.-955-2246G>A (p.=) n.1059-2246G>A (p.=) | dbSNP |

9 | g.116865982A>C | CA199061070 | ASTN2 | c.1737-2249T>G (p.=) c.1890-2249T>G (p.=) c.1878-2249T>G (p.=) c.-955-2249T>G (p.=) n.1059-2249T>G (p.=) | dbSNP gnomAD |

9 | g.116865987C>T | CA859193050 | ASTN2 | c.1737-2254G>A (p.=) c.1890-2254G>A (p.=) c.1878-2254G>A (p.=) c.-955-2254G>A (p.=) n.1059-2254G>A (p.=) | |

9 | g.116865989A>C | CA199061071 | ASTN2 | c.1737-2256T>G (p.=) c.1890-2256T>G (p.=) c.1878-2256T>G (p.=) c.-955-2256T>G (p.=) n.1059-2256T>G (p.=) | dbSNP |

9 | g.116865990C>T | CA199061073 | ASTN2 | c.1737-2257G>A (p.=) c.1890-2257G>A (p.=) c.1878-2257G>A (p.=) c.-955-2257G>A (p.=) n.1059-2257G>A (p.=) | dbSNP |

9 | g.116865990dup | CA199061072 | ASTN2 | c.1737-2257dup (p.=) c.1890-2257dup (p.=) c.1878-2257dup (p.=) c.-955-2257dup (p.=) n.1059-2257dup (p.=) | dbSNP gnomAD |

9 | g.116865991A>G | CA590340677 | ASTN2 | c.1737-2258T>C (p.=) c.1890-2258T>C (p.=) c.1878-2258T>C (p.=) c.-955-2258T>C (p.=) n.1059-2258T>C (p.=) | gnomAD |

9 | g.116865996C>G | CA199061074 | ASTN2 | c.1737-2263G>C (p.=) c.1890-2263G>C (p.=) c.1878-2263G>C (p.=) c.-955-2263G>C (p.=) n.1059-2263G>C (p.=) | dbSNP |

9 | g.116865998T>G | CA859193052 | ASTN2 | c.1737-2265A>C (p.=) c.1890-2265A>C (p.=) c.1878-2265A>C (p.=) c.-955-2265A>C (p.=) n.1059-2265A>C (p.=) | |

9 | g.116865999_116866000insG | CA590340680 | ASTN2 | c.1737-2267_1737-2266insC (p.=) c.1890-2267_1890-2266insC (p.=) c.1878-2267_1878-2266insC (p.=) c.-955-2267_-955-2266insC (p.=) n.1059-2267_1059-2266insC (p.=) | gnomAD |

9 | g.116866000A>G | CA199061075 | ASTN2 | c.1737-2267T>C (p.=) c.1890-2267T>C (p.=) c.1878-2267T>C (p.=) c.-955-2267T>C (p.=) n.1059-2267T>C (p.=) | dbSNP gnomAD |

9 | g.116866007C>T | CA199061076 | ASTN2 | c.1737-2274G>A (p.=) c.1890-2274G>A (p.=) c.1878-2274G>A (p.=) c.-955-2274G>A (p.=) n.1059-2274G>A (p.=) | dbSNP gnomAD |

9 | g.116866008G>A | CA590340682 | ASTN2 | c.1737-2275C>T (p.=) c.1890-2275C>T (p.=) c.1878-2275C>T (p.=) c.-955-2275C>T (p.=) n.1059-2275C>T (p.=) | gnomAD |

9 | g.116866009C>G | CA199061077 | ASTN2 | c.1737-2276G>C (p.=) c.1890-2276G>C (p.=) c.1878-2276G>C (p.=) c.-955-2276G>C (p.=) n.1059-2276G>C (p.=) | dbSNP |

9 | g.116866010C>T | CA859193058 | ASTN2 | c.1737-2277G>A (p.=) c.1890-2277G>A (p.=) c.1878-2277G>A (p.=) c.-955-2277G>A (p.=) n.1059-2277G>A (p.=) | |

9 | g.116866026C>A | CA590340683 | ASTN2 | c.1737-2293G>T (p.=) c.1890-2293G>T (p.=) c.1878-2293G>T (p.=) c.-955-2293G>T (p.=) n.1059-2293G>T (p.=) | gnomAD |

9 | g.116866026C>G | CA199061078 | ASTN2 | c.1737-2293G>C (p.=) c.1890-2293G>C (p.=) c.1878-2293G>C (p.=) c.-955-2293G>C (p.=) n.1059-2293G>C (p.=) | dbSNP |

9 | g.116866035C>T | CA590340684 | ASTN2 | c.1737-2302G>A (p.=) c.1890-2302G>A (p.=) c.1878-2302G>A (p.=) c.-955-2302G>A (p.=) n.1059-2302G>A (p.=) | gnomAD |

9 | g.116866038C>A | CA859193063 | ASTN2 | c.1737-2305G>T (p.=) c.1890-2305G>T (p.=) c.1878-2305G>T (p.=) c.-955-2305G>T (p.=) n.1059-2305G>T (p.=) | |

9 | g.116866057T>C | CA199061079 | ASTN2 | c.1737-2324A>G (p.=) c.1890-2324A>G (p.=) c.1878-2324A>G (p.=) c.-955-2324A>G (p.=) n.1059-2324A>G (p.=) | dbSNP gnomAD |

9 | g.116866069C>G | CA199061080 | ASTN2 | c.1737-2336G>C (p.=) c.1890-2336G>C (p.=) c.1878-2336G>C (p.=) c.-955-2336G>C (p.=) n.1059-2336G>C (p.=) | dbSNP |

9 | g.116866071T>C | CA199061081 | ASTN2 | c.1737-2338A>G (p.=) c.1890-2338A>G (p.=) c.1878-2338A>G (p.=) c.-955-2338A>G (p.=) n.1059-2338A>G (p.=) | dbSNP gnomAD |

9 | g.116866073G>A | CA199061082 | ASTN2 | c.1737-2340C>T (p.=) c.1890-2340C>T (p.=) c.1878-2340C>T (p.=) c.-955-2340C>T (p.=) n.1059-2340C>T (p.=) | dbSNP gnomAD |

9 | g.116866074T>C | CA590340685 | ASTN2 | c.1737-2341A>G (p.=) c.1890-2341A>G (p.=) c.1878-2341A>G (p.=) c.-955-2341A>G (p.=) n.1059-2341A>G (p.=) | gnomAD |

9 | g.116866076G>C | CA199061083 | ASTN2 | c.1737-2343C>G (p.=) c.1890-2343C>G (p.=) c.1878-2343C>G (p.=) c.-955-2343C>G (p.=) n.1059-2343C>G (p.=) | dbSNP |