| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.118473878C>G | CA382817328 | KMT2A | c.2818C>G (p.Pro940Ala) c.602-301C>G (n.602-301C>G) c.503-301C>G (n.503-301C>G) c.827-301C>G (n.827-301C>G) c.2719C>G (p.Pro907Ala) c.272-301C>G (n.272-301C>G) c.1489C>G (p.Pro497Ala) c.413-301C>G (n.413-301C>G) c.353-301C>G (n.353-301C>G) c.254-301C>G (n.254-301C>G) c.926-301C>G (n.926-301C>G) | dbSNP |
| 11 | g.118473878C>T | CA16619275 | KMT2A | c.2818C>T (p.Pro940Ser) c.602-301C>T (n.602-301C>T) c.503-301C>T (n.503-301C>T) c.827-301C>T (n.827-301C>T) c.2719C>T (p.Pro907Ser) c.272-301C>T (n.272-301C>T) c.1489C>T (p.Pro497Ser) c.413-301C>T (n.413-301C>T) c.353-301C>T (n.353-301C>T) c.254-301C>T (n.254-301C>T) c.926-301C>T (n.926-301C>T) | ClinVar dbSNP |