| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.152148810G>A | CA16605296 | KMT2C | c.1305C>T n.2249C>T c.13288C>T (p.Pro4430Ser) n.2417C>T n.8309C>T c.3690C>T c.10627C>T (p.Pro3543Ser) n.4747C>T c.3762C>T n.1883C>T n.1833C>T c.1534C>T (p.Pro512Ser) c.8014C>T (p.Pro2672Ser) c.13117C>T (p.Pro4373Ser) c.8904C>T c.3759C>T c.3693C>T n.7828C>T c.8017C>T (p.Pro2673Ser) c.12682C>T (p.Pro4228Ser) c.3694C>T n.2132C>T c.5798C>T c.2968C>T (p.Pro990Ser) n.10999C>T c.*10637C>T (n.*10637C>T) c.13333C>T (p.Pro4445Ser) c.13330C>T (p.Pro4444Ser) c.13168C>T (p.Pro4390Ser) c.13261C>T (p.Pro4421Ser) c.13165C>T (p.Pro4389Ser) c.13285C>T (p.Pro4429Ser) c.13213C>T (p.Pro4405Ser) c.13180C>T (p.Pro4394Ser) c.13096C>T (p.Pro4366Ser) c.12418C>T (p.Pro4140Ser) c.10879C>T (p.Pro3627Ser) c.13300C>T (p.Pro4434Ser) c.13282C>T (p.Pro4428Ser) c.13258C>T (p.Pro4420Ser) c.13186C>T (p.Pro4396Ser) c.13150C>T (p.Pro4384Ser) c.10003C>T (p.Pro3335Ser) c.9607C>T (p.Pro3203Ser) | ClinVar dbSNP |
| 7 | g.152148810G>C | CA370093127 | KMT2C | c.1305C>G n.2249C>G c.13288C>G (p.Pro4430Ala) n.2417C>G n.8309C>G c.3690C>G c.10627C>G (p.Pro3543Ala) n.4747C>G c.3762C>G n.1883C>G n.1833C>G c.1534C>G (p.Pro512Ala) c.8014C>G (p.Pro2672Ala) c.13117C>G (p.Pro4373Ala) c.8904C>G c.3759C>G c.3693C>G n.7828C>G c.8017C>G (p.Pro2673Ala) c.12682C>G (p.Pro4228Ala) c.3694C>G n.2132C>G c.5798C>G c.2968C>G (p.Pro990Ala) n.10999C>G c.*10637C>G (n.*10637C>G) c.13333C>G (p.Pro4445Ala) c.13330C>G (p.Pro4444Ala) c.13168C>G (p.Pro4390Ala) c.13261C>G (p.Pro4421Ala) c.13165C>G (p.Pro4389Ala) c.13285C>G (p.Pro4429Ala) c.13213C>G (p.Pro4405Ala) c.13180C>G (p.Pro4394Ala) c.13096C>G (p.Pro4366Ala) c.12418C>G (p.Pro4140Ala) c.10879C>G (p.Pro3627Ala) c.13300C>G (p.Pro4434Ala) c.13282C>G (p.Pro4428Ala) c.13258C>G (p.Pro4420Ala) c.13186C>G (p.Pro4396Ala) c.13150C>G (p.Pro4384Ala) c.10003C>G (p.Pro3335Ala) c.9607C>G (p.Pro3203Ala) | dbSNP |