| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.177283835A>T | CA16042519 | NSD1 | c.5185A>T (p.Asn1729Tyr) c.700A>T (p.Asn234Tyr) n.5641A>T c.5749A>T (p.Asn1917Tyr) n.5455A>T n.6205A>T n.4607A>T c.6058A>T (p.Asn2020Tyr) c.5251A>T (p.Asn1751Tyr) c.1552A>T (p.Asn518Tyr) c.5638A>T (p.Asn1880Tyr) c.5002A>T (p.Asn1668Tyr) c.1792A>T (p.Asn598Tyr) | ClinVar dbSNP |
| 5 | g.177283835A= | CA1603553560 | NSD1 | c.5185A= (p.Asn1729=) c.700A= (p.Asn234=) n.5641A= c.5749A= (p.Asn1917=) n.5455A= n.6205A= n.4607A= c.6058A= (p.Asn2020=) c.5251A= (p.Asn1751=) c.1552A= (p.Asn518=) c.5638A= (p.Asn1880=) c.5002A= (p.Asn1668=) c.1792A= (p.Asn598=) | dbSNP |