Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157207109C>GCA366248049ARID1Bc.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
6g.157207109C>TCA209106ARID1Bc.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

Number of alleles fetched