| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89281609del | CA16620305 | ANKRD11 | c.4933del (p.Leu1645TrpfsTer?) c.*4736del (n.*4736del) c.745-6418del (n.745-6418del) c.152-6418del c.4831del (p.Leu1611TrpfsTer?) c.4636del (p.Leu1546TrpfsTer?) c.4804del (p.Leu1602TrpfsTer?) | ClinVar dbSNP |
| 16 | g.89281609G= | CA2241602208 | ANKRD11 | c.4933C= (p.Leu1645=) c.*4736C= (n.*4736C=) c.745-6418C= (n.745-6418C=) c.152-6418C= c.4831C= (p.Leu1611=) c.4636C= (p.Leu1546=) c.4804C= (p.Leu1602=) | dbSNP dbSNP |