| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.118476841G>A | CA382823653 | KMT2A | c.3292G>A (p.Gly1098Arg) c.775G>A (p.Gly259Arg) c.676G>A (p.Gly226Arg) c.1000G>A (p.Gly334Arg) c.174G>A c.3193G>A (p.Gly1065Arg) c.445G>A (p.Gly149Arg) c.1963G>A (p.Gly655Arg) c.427G>A (p.Gly143Arg) c.1099G>A (p.Gly367Arg) | dbSNP |
| 11 | g.118476841G>T | CA16621629 | KMT2A | c.3292G>T (p.Gly1098Ter) c.775G>T (p.Gly259Ter) c.676G>T (p.Gly226Ter) c.1000G>T (p.Gly334Ter) c.174G>T c.3193G>T (p.Gly1065Ter) c.445G>T (p.Gly149Ter) c.1963G>T (p.Gly655Ter) c.427G>T (p.Gly143Ter) c.1099G>T (p.Gly367Ter) | ClinVar dbSNP |