| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.177257097C>T | CA16618177 | NSD1 | c.4039C>T (p.His1347Tyr) n.4495C>T c.4603C>T (p.His1535Tyr) n.4309C>T n.5059C>T c.4912C>T (p.His1638Tyr) c.4105C>T (p.His1369Tyr) c.406C>T (p.His136Tyr) c.4492C>T (p.His1498Tyr) c.3856C>T (p.His1286Tyr) c.646C>T (p.His216Tyr) | ClinVar dbSNP |
| 5 | g.177257097C= | CA1603536685 | NSD1 | c.4039C= (p.His1347=) n.4495C= c.4603C= (p.His1535=) n.4309C= n.5059C= c.4912C= (p.His1638=) c.4105C= (p.His1369=) c.406C= (p.His136=) c.4492C= (p.His1498=) c.3856C= (p.His1286=) c.646C= (p.His216=) | dbSNP |