Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.157207109C>G | CA366248049 | ARID1B | c.6178C>G (p.Arg2060Gly) c.6247C>G (p.Arg2083Gly) c.6466C>G (p.Arg2156Gly) c.6217C>G (p.Arg2073Gly) c.5929C>G (p.Arg1977Gly) c.4495C>G (p.Arg1499Gly) c.3658C>G (p.Arg1220Gly) c.493C>G (p.Arg165Gly) c.3289C>G (p.Arg1097Gly) n.4800C>G n.2257C>G c.6337C>G (p.Arg2113Gly) n.4334C>G c.3705C>G c.3619C>G n.3003C>G c.3679C>G (p.Arg1227Gly) c.3838C>G (p.Arg1280Gly) n.3452C>G c.5968C>G (p.Arg1990Gly) c.6088C>G (p.Arg2030Gly) c.5167C>G (p.Arg1723Gly) c.4987C>G (p.Arg1663Gly) c.4747C>G (p.Arg1583Gly) c.4366C>G (p.Arg1456Gly) c.3229C>G (p.Arg1077Gly) c.6298C>G (p.Arg2100Gly) c.6199C>G (p.Arg2067Gly) c.6169C>G (p.Arg2057Gly) c.6139C>G (p.Arg2047Gly) c.6010C>G (p.Arg2004Gly) c.5989C>G (p.Arg1997Gly) n.6284C>G | dbSNP gnomAD v4 |
6 | g.157207109C>T | CA209106 | ARID1B | c.6178C>T (p.Arg2060Ter) c.6247C>T (p.Arg2083Ter) c.6466C>T (p.Arg2156Ter) c.6217C>T (p.Arg2073Ter) c.5929C>T (p.Arg1977Ter) c.4495C>T (p.Arg1499Ter) c.3658C>T (p.Arg1220Ter) c.493C>T (p.Arg165Ter) c.3289C>T (p.Arg1097Ter) n.4800C>T n.2257C>T c.6337C>T (p.Arg2113Ter) n.4334C>T c.3705C>T c.3619C>T n.3003C>T c.3679C>T (p.Arg1227Ter) c.3838C>T (p.Arg1280Ter) n.3452C>T c.5968C>T (p.Arg1990Ter) c.6088C>T (p.Arg2030Ter) c.5167C>T (p.Arg1723Ter) c.4987C>T (p.Arg1663Ter) c.4747C>T (p.Arg1583Ter) c.4366C>T (p.Arg1456Ter) c.3229C>T (p.Arg1077Ter) c.6298C>T (p.Arg2100Ter) c.6199C>T (p.Arg2067Ter) c.6169C>T (p.Arg2057Ter) c.6139C>T (p.Arg2047Ter) c.6010C>T (p.Arg2004Ter) c.5989C>T (p.Arg1997Ter) n.6284C>T | ClinVar dbSNP COSMIC |