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

1 | g.156138759T>C | CA347066 | LMNA | c.1632+2T>C (p.=) c.1818+152T>C (p.=) c.1968+2T>C (p.=) c.1878+2T>C (p.=) c.1344+2T>C (p.=) n.2257+2T>C n.2255+2T>C c.1671+2T>C (p.=) n.2181+2T>C n.552+2T>C n.756+2T>C (p.=) | ClinVar dbSNP |

1 | g.156138759T>A | CA347065 | LMNA | c.1632+2T>A (p.=) c.1818+152T>A (p.=) c.1968+2T>A (p.=) c.1878+2T>A (p.=) c.1344+2T>A (p.=) n.2257+2T>A n.2255+2T>A c.1671+2T>A (p.=) n.2181+2T>A n.552+2T>A n.756+2T>A (p.=) | ClinVar dbSNP |

1 | g.156138759T>G | CA31015743 | LMNA | c.1632+2T>G (p.=) c.1818+152T>G (p.=) c.1968+2T>G (p.=) c.1878+2T>G (p.=) c.1344+2T>G (p.=) n.2257+2T>G n.2255+2T>G c.1671+2T>G (p.=) n.2181+2T>G n.552+2T>G n.756+2T>G (p.=) | dbSNP |