| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.157200930C>T | CA206215 | ARID1B | c.4546C>T (p.Gln1516Ter) c.4615C>T (p.Gln1539Ter) c.4834C>T (p.Gln1612Ter) c.4585C>T (p.Gln1529Ter) c.4297C>T (p.Gln1433Ter) c.2863C>T (p.Gln955Ter) c.2026C>T (p.Gln676Ter) c.1657C>T (p.Gln553Ter) n.3168C>T n.625C>T c.4705C>T (p.Gln1569Ter) n.2702C>T c.2073C>T c.1987C>T n.1371C>T c.2047C>T (p.Gln683Ter) c.2206C>T (p.Gln736Ter) c.4336C>T (p.Gln1446Ter) c.4456C>T (p.Gln1486Ter) c.3535C>T (p.Gln1179Ter) c.3355C>T (p.Gln1119Ter) c.3115C>T (p.Gln1039Ter) c.2734C>T (p.Gln912Ter) c.1597C>T (p.Gln533Ter) c.4666C>T (p.Gln1556Ter) c.4567C>T (p.Gln1523Ter) c.4537C>T (p.Gln1513Ter) c.4507C>T (p.Gln1503Ter) c.4378C>T (p.Gln1460Ter) c.4357C>T (p.Gln1453Ter) n.4652C>T | ClinVar dbSNP |
| 6 | g.157200930C= | CA1675543150 | ARID1B | c.4546C= (p.Gln1516=) c.4615C= (p.Gln1539=) c.4834C= (p.Gln1612=) c.4585C= (p.Gln1529=) c.4297C= (p.Gln1433=) c.2863C= (p.Gln955=) c.2026C= (p.Gln676=) c.1657C= (p.Gln553=) n.3168C= n.625C= c.4705C= (p.Gln1569=) n.2702C= c.2073C= c.1987C= n.1371C= c.2047C= (p.Gln683=) c.2206C= (p.Gln736=) c.4336C= (p.Gln1446=) c.4456C= (p.Gln1486=) c.3535C= (p.Gln1179=) c.3355C= (p.Gln1119=) c.3115C= (p.Gln1039=) c.2734C= (p.Gln912=) c.1597C= (p.Gln533=) c.4666C= (p.Gln1556=) c.4567C= (p.Gln1523=) c.4537C= (p.Gln1513=) c.4507C= (p.Gln1503=) c.4378C= (p.Gln1460=) c.4357C= (p.Gln1453=) n.4652C= | dbSNP |