| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.177257010delinsGA | CA16042594 | NSD1 | c.3952delinsGA (p.Pro1318AspfsTer9) n.4408delinsGA c.4516delinsGA (p.Pro1506AspfsTer9) n.4222delinsGA n.4972delinsGA c.4825delinsGA (p.Pro1609AspfsTer9) c.4018delinsGA (p.Pro1340AspfsTer9) c.319delinsGA (p.Pro107AspfsTer9) c.4405delinsGA (p.Pro1469AspfsTer9) c.3769delinsGA (p.Pro1257AspfsTer9) c.559delinsGA (p.Pro187AspfsTer9) | ClinVar dbSNP |
| 5 | g.177257010C= | CA3124061295 | NSD1 | c.3952C= (p.Pro1318=) n.4408C= c.4516C= (p.Pro1506=) n.4222C= n.4972C= c.4825C= (p.Pro1609=) c.4018C= (p.Pro1340=) c.319C= (p.Pro107=) c.4405C= (p.Pro1469=) c.3769C= (p.Pro1257=) c.559C= (p.Pro187=) | dbSNP |