| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.21730926G>C | CA5435078 | MLLT10 | c.2090G>C (p.Arg697Pro) c.2138G>C (p.Arg713Pro) c.1174G>C c.*2109G>C (n.*2109G>C) c.*2091G>C (n.*2091G>C) n.3113G>C c.1067G>C (p.Arg356Pro) c.2057G>C (p.Arg686Pro) c.2192G>C (p.Arg731Pro) c.2159G>C (p.Arg720Pro) c.2105G>C (p.Arg702Pro) c.2096G>C (p.Arg699Pro) c.1958G>C (p.Arg653Pro) c.1835G>C (p.Arg612Pro) c.1832G>C (p.Arg611Pro) c.1421G>C (p.Arg474Pro) n.2363G>C c.1355G>C (p.Arg452Pro) n.2735G>C c.1733G>C (p.Arg578Pro) c.1574G>C (p.Arg525Pro) c.1457G>C (p.Arg486Pro) n.1011-3863C>G n.2675G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.21730926G>A | CA5435077 | MLLT10 | c.2090G>A (p.Arg697His) c.2138G>A (p.Arg713His) c.1174G>A c.*2109G>A (n.*2109G>A) c.*2091G>A (n.*2091G>A) n.3113G>A c.1067G>A (p.Arg356His) c.2057G>A (p.Arg686His) c.2192G>A (p.Arg731His) c.2159G>A (p.Arg720His) c.2105G>A (p.Arg702His) c.2096G>A (p.Arg699His) c.1958G>A (p.Arg653His) c.1835G>A (p.Arg612His) c.1832G>A (p.Arg611His) c.1421G>A (p.Arg474His) n.2363G>A c.1355G>A (p.Arg452His) n.2735G>A c.1733G>A (p.Arg578His) c.1574G>A (p.Arg525His) c.1457G>A (p.Arg486His) n.1011-3863C>T n.2675G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.21730926G= | CA1895821746 | MLLT10 | c.2090G= (p.Arg697=) c.2138G= (p.Arg713=) c.1174G= c.*2109G= (n.*2109G=) c.*2091G= (n.*2091G=) n.3113G= c.1067G= (p.Arg356=) c.2057G= (p.Arg686=) c.2192G= (p.Arg731=) c.2159G= (p.Arg720=) c.2105G= (p.Arg702=) c.2096G= (p.Arg699=) c.1958G= (p.Arg653=) c.1835G= (p.Arg612=) c.1832G= (p.Arg611=) c.1421G= (p.Arg474=) n.2363G= c.1355G= (p.Arg452=) n.2735G= c.1733G= (p.Arg578=) c.1574G= (p.Arg525=) c.1457G= (p.Arg486=) n.1011-3863C= n.2675G= | dbSNP |