Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.17216429del | CA348602 | FLCN,MPRIP | c.1252del (p.Leu418TrpfsTer?) c.*86del (n.*86del) c.562-1061del c.1306del (p.Leu436TrpfsTer?) c.1030del (p.Leu344TrpfsTer?) n.2570+641del n.1734+641del | ClinVar dbSNP |
17 | g.17216429dup | CA2580092721 | FLCN,MPRIP | c.1252dup (p.Leu418ProfsTer?) c.*86dup (n.*86dup) c.562-1061dup c.1306dup (p.Leu436ProfsTer?) c.1030dup (p.Leu344ProfsTer?) n.2570+641dup n.1734+641dup | ClinVar dbSNP |