| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.75029229dup | CA213029 | DUSP29,KAT6B | c.4405dup (p.Ser1469PhefsTer18) c.3856dup (p.Ser1286PhefsTer18) c.3529dup (p.Ser1177PhefsTer18) n.577-2635dup c.*3622-2635dup (n.*3622-2635dup) c.4243dup (p.Ser1415PhefsTer18) c.3367dup (p.Ser1123PhefsTer18) c.2716dup (p.Ser906PhefsTer18) c.2320dup (p.Ser774PhefsTer18) c.2062dup (p.Ser688PhefsTer18) c.3340dup (p.Ser1114PhefsTer18) | ClinVar dbSNP |
| 10 | g.75029229T= | CA3173970601 | DUSP29,KAT6B | c.4405T= (p.Ser1469=) c.3856T= (p.Ser1286=) c.3529T= (p.Ser1177=) n.577-2635A= c.*3622-2635A= (n.*3622-2635A=) c.4243T= (p.Ser1415=) c.3367T= (p.Ser1123=) c.2716T= (p.Ser906=) c.2320T= (p.Ser774=) c.2062T= (p.Ser688=) c.3340T= (p.Ser1114=) | dbSNP |