| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.33738875C>T | CA16616935 | ASXL3 | c.1474C>T (p.Gln492Ter) c.1471C>T (p.Gln491Ter) c.*595C>T (n.*595C>T) c.*1130C>T (n.*1130C>T) c.1683C>T (n.1683C>T) c.1303C>T (p.Gln435Ter) c.1351C>T (p.Gln451Ter) c.1447C>T (p.Gln483Ter) c.1393C>T (p.Gln465Ter) c.1354C>T (p.Gln452Ter) | ClinVar dbSNP |
| 18 | g.33738875C= | CA2294855720 | ASXL3 | c.1474C= (p.Gln492=) c.1471C= (p.Gln491=) c.*595C= (n.*595C=) c.*1130C= (n.*1130C=) c.1683C= (n.1683C=) c.1303C= (p.Gln435=) c.1351C= (p.Gln451=) c.1447C= (p.Gln483=) c.1393C= (p.Gln465=) c.1354C= (p.Gln452=) | dbSNP |