| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.177282475T>C | CA16618184 | NSD1 | c.5030T>C (p.Val1677Ala) c.545T>C (p.Val182Ala) n.5486T>C c.5594T>C (p.Val1865Ala) n.5300T>C n.6050T>C n.4452T>C c.5903T>C (p.Val1968Ala) c.5096T>C (p.Val1699Ala) c.1397T>C (p.Val466Ala) c.5483T>C (p.Val1828Ala) c.4847T>C (p.Val1616Ala) c.1637T>C (p.Val546Ala) | ClinVar dbSNP |
| 5 | g.177282475T>A | CA362314398 | NSD1 | c.5030T>A (p.Val1677Glu) c.545T>A (p.Val182Glu) n.5486T>A c.5594T>A (p.Val1865Glu) n.5300T>A n.6050T>A n.4452T>A c.5903T>A (p.Val1968Glu) c.5096T>A (p.Val1699Glu) c.1397T>A (p.Val466Glu) c.5483T>A (p.Val1828Glu) c.4847T>A (p.Val1616Glu) c.1637T>A (p.Val546Glu) | dbSNP |
| 5 | g.177282475T>G | CA362314406 | NSD1 | c.5030T>G (p.Val1677Gly) c.545T>G (p.Val182Gly) n.5486T>G c.5594T>G (p.Val1865Gly) n.5300T>G n.6050T>G n.4452T>G c.5903T>G (p.Val1968Gly) c.5096T>G (p.Val1699Gly) c.1397T>G (p.Val466Gly) c.5483T>G (p.Val1828Gly) c.4847T>G (p.Val1616Gly) c.1637T>G (p.Val546Gly) | dbSNP |