Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157206545C>TCA206469ARID1Bc.5614C>T (p.Arg1872Ter)
c.5683C>T (p.Arg1895Ter)
c.5902C>T (p.Arg1968Ter)
c.5653C>T (p.Arg1885Ter)
c.5365C>T (p.Arg1789Ter)
c.3931C>T (p.Arg1311Ter)
c.3094C>T (p.Arg1032Ter)
c.2725C>T (p.Arg909Ter)
n.4236C>T
n.1693C>T
c.5773C>T (p.Arg1925Ter)
n.3770C>T
c.3141C>T
c.3055C>T
n.2439C>T
c.3115C>T (p.Arg1039Ter)
c.3274C>T (p.Arg1092Ter)
n.2888C>T
c.5404C>T (p.Arg1802Ter)
c.5524C>T (p.Arg1842Ter)
c.4603C>T (p.Arg1535Ter)
c.4423C>T (p.Arg1475Ter)
c.4183C>T (p.Arg1395Ter)
c.3802C>T (p.Arg1268Ter)
c.2665C>T (p.Arg889Ter)
c.5734C>T (p.Arg1912Ter)
c.5635C>T (p.Arg1879Ter)
c.5605C>T (p.Arg1869Ter)
c.5575C>T (p.Arg1859Ter)
c.5446C>T (p.Arg1816Ter)
c.5425C>T (p.Arg1809Ter)
n.5720C>T
ClinVar dbSNP COSMIC COSMIC
6g.157206545C=CA1675530508ARID1Bc.5614C= (p.Arg1872=)
c.5683C= (p.Arg1895=)
c.5902C= (p.Arg1968=)
c.5653C= (p.Arg1885=)
c.5365C= (p.Arg1789=)
c.3931C= (p.Arg1311=)
c.3094C= (p.Arg1032=)
c.2725C= (p.Arg909=)
n.4236C=
n.1693C=
c.5773C= (p.Arg1925=)
n.3770C=
c.3141C=
c.3055C=
n.2439C=
c.3115C= (p.Arg1039=)
c.3274C= (p.Arg1092=)
n.2888C=
c.5404C= (p.Arg1802=)
c.5524C= (p.Arg1842=)
c.4603C= (p.Arg1535=)
c.4423C= (p.Arg1475=)
c.4183C= (p.Arg1395=)
c.3802C= (p.Arg1268=)
c.2665C= (p.Arg889=)
c.5734C= (p.Arg1912=)
c.5635C= (p.Arg1879=)
c.5605C= (p.Arg1869=)
c.5575C= (p.Arg1859=)
c.5446C= (p.Arg1816=)
c.5425C= (p.Arg1809=)
n.5720C=
dbSNP
6g.157206545C>ACA452978477ARID1Bc.5614C>A (p.Arg1872=)
c.5683C>A (p.Arg1895=)
c.5902C>A (p.Arg1968=)
c.5653C>A (p.Arg1885=)
c.5365C>A (p.Arg1789=)
c.3931C>A (p.Arg1311=)
c.3094C>A (p.Arg1032=)
c.2725C>A (p.Arg909=)
n.4236C>A
n.1693C>A
c.5773C>A (p.Arg1925=)
n.3770C>A
c.3141C>A
c.3055C>A
n.2439C>A
c.3115C>A (p.Arg1039=)
c.3274C>A (p.Arg1092=)
n.2888C>A
c.5404C>A (p.Arg1802=)
c.5524C>A (p.Arg1842=)
c.4603C>A (p.Arg1535=)
c.4423C>A (p.Arg1475=)
c.4183C>A (p.Arg1395=)
c.3802C>A (p.Arg1268=)
c.2665C>A (p.Arg889=)
c.5734C>A (p.Arg1912=)
c.5635C>A (p.Arg1879=)
c.5605C>A (p.Arg1869=)
c.5575C>A (p.Arg1859=)
c.5446C>A (p.Arg1816=)
c.5425C>A (p.Arg1809=)
n.5720C>A
dbSNP gnomAD v4

Number of alleles fetched