| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.75029925C>T | CA10603066 | DUSP29,KAT6B | c.5101C>T (p.Gln1701Ter) c.4552C>T (p.Gln1518Ter) c.4225C>T (p.Gln1409Ter) n.577-3331G>A c.*3622-3331G>A (n.*3622-3331G>A) c.4939C>T (p.Gln1647Ter) c.4063C>T (p.Gln1355Ter) c.3412C>T (p.Gln1138Ter) c.3016C>T (p.Gln1006Ter) c.2758C>T (p.Gln920Ter) c.4036C>T (p.Gln1346Ter) | ClinVar dbSNP |
| 10 | g.75029925C= | CA1920306882 | DUSP29,KAT6B | c.5101C= (p.Gln1701=) c.4552C= (p.Gln1518=) c.4225C= (p.Gln1409=) n.577-3331G= c.*3622-3331G= (n.*3622-3331G=) c.4939C= (p.Gln1647=) c.4063C= (p.Gln1355=) c.3412C= (p.Gln1138=) c.3016C= (p.Gln1006=) c.2758C= (p.Gln920=) c.4036C= (p.Gln1346=) | dbSNP |