| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.75030213C>T | CA143738 | DUSP29,KAT6B | c.5389C>T (p.Arg1797Ter) c.4840C>T (p.Arg1614Ter) c.4513C>T (p.Arg1505Ter) n.577-3619G>A c.*3622-3619G>A (n.*3622-3619G>A) c.5227C>T (p.Arg1743Ter) c.4351C>T (p.Arg1451Ter) c.3700C>T (p.Arg1234Ter) c.3304C>T (p.Arg1102Ter) c.3046C>T (p.Arg1016Ter) c.4324C>T (p.Arg1442Ter) | ClinVar dbSNP COSMIC |
| 10 | g.75030213C= | CA1920306994 | DUSP29,KAT6B | c.5389C= (p.Arg1797=) c.4840C= (p.Arg1614=) c.4513C= (p.Arg1505=) n.577-3619G= c.*3622-3619G= (n.*3622-3619G=) c.5227C= (p.Arg1743=) c.4351C= (p.Arg1451=) c.3700C= (p.Arg1234=) c.3304C= (p.Arg1102=) c.3046C= (p.Arg1016=) c.4324C= (p.Arg1442=) | dbSNP |
| 10 | g.75030213C>A | CA470300852 | DUSP29,KAT6B | c.5389C>A (p.Arg1797=) c.4840C>A (p.Arg1614=) c.4513C>A (p.Arg1505=) n.577-3619G>T c.*3622-3619G>T (n.*3622-3619G>T) c.5227C>A (p.Arg1743=) c.4351C>A (p.Arg1451=) c.3700C>A (p.Arg1234=) c.3304C>A (p.Arg1102=) c.3046C>A (p.Arg1016=) c.4324C>A (p.Arg1442=) | dbSNP gnomAD v4 |