| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89282337dup | CA645294091 | ANKRD11 | c.4205dup (p.Tyr1402Ter) c.*4008dup (n.*4008dup) c.744+6191dup (n.744+6191dup) c.151+6191dup c.4103dup (p.Tyr1368Ter) c.3908dup (p.Tyr1303Ter) c.4076dup (p.Tyr1359Ter) | ClinVar dbSNP |
| 16 | g.89282337T= | CA3217832168 | ANKRD11 | c.4205A= (p.Tyr1402=) c.*4008A= (n.*4008A=) c.744+6191A= (n.744+6191A=) c.151+6191A= c.4103A= (p.Tyr1368=) c.3908A= (p.Tyr1303=) c.4076A= (p.Tyr1359=) | dbSNP dbSNP |