| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.157201050C>T | CA16618266 | ARID1B | c.4666C>T (p.Gln1556Ter) c.4735C>T (p.Gln1579Ter) c.4954C>T (p.Gln1652Ter) c.4705C>T (p.Gln1569Ter) c.4417C>T (p.Gln1473Ter) c.2983C>T (p.Gln995Ter) c.2146C>T (p.Gln716Ter) c.1777C>T (p.Gln593Ter) n.3288C>T n.745C>T c.4825C>T (p.Gln1609Ter) n.2822C>T c.2193C>T c.2107C>T n.1491C>T c.2167C>T (p.Gln723Ter) c.2326C>T (p.Gln776Ter) c.4456C>T (p.Gln1486Ter) c.4576C>T (p.Gln1526Ter) c.3655C>T (p.Gln1219Ter) c.3475C>T (p.Gln1159Ter) c.3235C>T (p.Gln1079Ter) c.2854C>T (p.Gln952Ter) c.1717C>T (p.Gln573Ter) c.4786C>T (p.Gln1596Ter) c.4687C>T (p.Gln1563Ter) c.4657C>T (p.Gln1553Ter) c.4627C>T (p.Gln1543Ter) c.4498C>T (p.Gln1500Ter) c.4477C>T (p.Gln1493Ter) n.4772C>T | ClinVar dbSNP |
| 6 | g.157201050C= | CA1675522870 | ARID1B | c.4666C= (p.Gln1556=) c.4735C= (p.Gln1579=) c.4954C= (p.Gln1652=) c.4705C= (p.Gln1569=) c.4417C= (p.Gln1473=) c.2983C= (p.Gln995=) c.2146C= (p.Gln716=) c.1777C= (p.Gln593=) n.3288C= n.745C= c.4825C= (p.Gln1609=) n.2822C= c.2193C= c.2107C= n.1491C= c.2167C= (p.Gln723=) c.2326C= (p.Gln776=) c.4456C= (p.Gln1486=) c.4576C= (p.Gln1526=) c.3655C= (p.Gln1219=) c.3475C= (p.Gln1159=) c.3235C= (p.Gln1079=) c.2854C= (p.Gln952=) c.1717C= (p.Gln573=) c.4786C= (p.Gln1596=) c.4687C= (p.Gln1563=) c.4657C= (p.Gln1553=) c.4627C= (p.Gln1543=) c.4498C= (p.Gln1500=) c.4477C= (p.Gln1493=) n.4772C= | dbSNP |