Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157110561G>ACA16042661ARID1Bc.2581G>A (p.Gly861Ser)
c.2492-22467G>A (n.2492-22467G>A)
c.595G>A (p.Gly199Ser)
c.2620G>A (p.Gly874Ser)
c.2332G>A (p.Gly778Ser)
c.740-22467G>A (n.740-22467G>A)
n.482G>A
n.230G>A
c.82G>A (p.Gly28Ser)
c.2371G>A (p.Gly791Ser)
n.1330G>A
c.598G>A (p.Gly200Ser)
n.440G>A
c.1282G>A (p.Gly428Ser)
c.862G>A (p.Gly288Ser)
c.481G>A (p.Gly161Ser)
c.2413G>A (p.Gly805Ser)
n.2496G>A
ClinVar dbSNP COSMIC COSMIC
6g.157110561G=CA1675498995ARID1Bc.2581G= (p.Gly861=)
c.2492-22467G= (n.2492-22467G=)
c.595G= (p.Gly199=)
c.2620G= (p.Gly874=)
c.2332G= (p.Gly778=)
c.740-22467G= (n.740-22467G=)
n.482G=
n.230G=
c.82G= (p.Gly28=)
c.2371G= (p.Gly791=)
n.1330G=
c.598G= (p.Gly200=)
n.440G=
c.1282G= (p.Gly428=)
c.862G= (p.Gly288=)
c.481G= (p.Gly161=)
c.2413G= (p.Gly805=)
n.2496G=
dbSNP

Number of alleles fetched