Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.157110561G>A | CA16042661 | ARID1B | c.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 |
6 | g.157110561G= | CA1675498995 | ARID1B | c.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 |