| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.75028893G>T | CA129312 | DUSP29,KAT6B | c.4069G>T (p.Glu1357Ter) c.3520G>T (p.Glu1174Ter) c.3193G>T (p.Glu1065Ter) n.577-2299C>A c.*3622-2299C>A (n.*3622-2299C>A) c.3907G>T (p.Glu1303Ter) c.3031G>T (p.Glu1011Ter) c.2380G>T (p.Glu794Ter) c.1984G>T (p.Glu662Ter) c.1726G>T (p.Glu576Ter) c.3004G>T (p.Glu1002Ter) | ClinVar dbSNP |
| 10 | g.75028893G= | CA1920306498 | DUSP29,KAT6B | c.4069G= (p.Glu1357=) c.3520G= (p.Glu1174=) c.3193G= (p.Glu1065=) n.577-2299C= c.*3622-2299C= (n.*3622-2299C=) c.3907G= (p.Glu1303=) c.3031G= (p.Glu1011=) c.2380G= (p.Glu794=) c.1984G= (p.Glu662=) c.1726G= (p.Glu576=) c.3004G= (p.Glu1002=) | dbSNP |