Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.156778665_156778763delCA2680909077ARID1Bc.985_1083del (p.Gly329_Gly361del)
c.736_834del (p.Gly246_Gly278del)
c.725_823del
n.819_917del
gnomAD v4
6g.156778698G>ACA366382814ARID1Bc.1018G>A (p.Gly340Arg)
c.769G>A (p.Gly257Arg)
c.758G>A
n.852G>A
gnomAD v4
6g.156778698G>CCA366382816ARID1Bc.1018G>C (p.Gly340Arg)
c.769G>C (p.Gly257Arg)
c.758G>C
n.852G>C
6g.156778698G=CA1675343676ARID1Bc.1018G= (p.Gly340=)
c.769G= (p.Gly257=)
c.758G=
n.852G=
6g.156778698G>TCA16042552ARID1Bc.1018G>T (p.Gly340Ter)
c.769G>T (p.Gly257Ter)
c.758G>T
n.852G>T
ClinVar dbSNP gnomAD v4
6g.156778699delCA2680909098ARID1Bc.1019del (p.Gly340AspfsTer9)
c.770del (p.Gly257AspfsTer9)
c.759del
n.853del
gnomAD v4
6g.156778699G>ACA366382820ARID1Bc.1019G>A (p.Gly340Glu)
c.770G>A (p.Gly257Glu)
c.759G>A
n.853G>A
dbSNP gnomAD v4
6g.156778699G>CCA366382819ARID1Bc.1019G>C (p.Gly340Ala)
c.770G>C (p.Gly257Ala)
c.759G>C
n.853G>C
6g.156778699G=CA1675343677ARID1Bc.1019G= (p.Gly340=)
c.770G= (p.Gly257=)
c.759G=
n.853G=
6g.156778699G>TCA366382822ARID1Bc.1019G>T (p.Gly340Val)
c.770G>T (p.Gly257Val)
c.759G>T
n.853G>T
dbSNP gnomAD v4
6g.156778700A>CCA452989073ARID1Bc.1020A>C (p.Gly340=)
c.771A>C (p.Gly257=)
c.760A>C
n.854A>C
dbSNP
6g.156778700A>GCA452989076ARID1Bc.1020A>G (p.Gly340=)
c.771A>G (p.Gly257=)
c.760A>G
n.854A>G
dbSNP gnomAD v4
6g.156778700A>TCA452989079ARID1Bc.1020A>T (p.Gly340=)
c.771A>T (p.Gly257=)
c.760A>T
n.854A>T
6g.156778701C>ACA366382824ARID1Bc.1021C>A (p.Gln341Lys)
c.772C>A (p.Gln258Lys)
c.761C>A
n.855C>A
6g.156778701C=CA1675343678ARID1Bc.1021C= (p.Gln341=)
c.772C= (p.Gln258=)
c.761C=
n.855C=
6g.156778701C>GCA366382826ARID1Bc.1021C>G (p.Gln341Glu)
c.772C>G (p.Gln258Glu)
c.761C>G
n.855C>G
dbSNP gnomAD v4
6g.156778701C>TCA366382827ARID1Bc.1021C>T (p.Gln341Ter)
c.772C>T (p.Gln258Ter)
c.761C>T
n.855C>T
ClinVar gnomAD v4
6g.156778702A>CCA366382830ARID1Bc.1022A>C (p.Gln341Pro)
c.773A>C (p.Gln258Pro)
c.762A>C
n.856A>C
gnomAD v4
6g.156778702A>GCA366382832ARID1Bc.1022A>G (p.Gln341Arg)
c.773A>G (p.Gln258Arg)
c.762A>G
n.856A>G
6g.156778702A>TCA366382833ARID1Bc.1022A>T (p.Gln341Leu)
c.773A>T (p.Gln258Leu)
c.762A>T
n.856A>T
6g.156778703A>CCA366382836ARID1Bc.1023A>C (p.Gln341His)
c.774A>C (p.Gln258His)
c.763A>C
n.857A>C
6g.156778703A>GCA452989087ARID1Bc.1023A>G (p.Gln341=)
c.774A>G (p.Gln258=)
c.763A>G
n.857A>G
gnomAD v4
6g.156778703A>TCA366382838ARID1Bc.1023A>T (p.Gln341His)
c.774A>T (p.Gln258His)
c.763A>T
n.857A>T
6g.156778704C>ACA366382840ARID1Bc.1024C>A (p.Gln342Lys)
c.775C>A (p.Gln259Lys)
c.764C>A
n.858C>A
gnomAD v4
6g.156778704C>GCA366382842ARID1Bc.1024C>G (p.Gln342Glu)
c.775C>G (p.Gln259Glu)
c.764C>G
n.858C>G
gnomAD v4
6g.156778704C>TCA366382843ARID1Bc.1024C>T (p.Gln342Ter)
c.775C>T (p.Gln259Ter)
c.764C>T
n.858C>T
gnomAD v4
6g.156778705A>CCA366382846ARID1Bc.1025A>C (p.Gln342Pro)
c.776A>C (p.Gln259Pro)
c.765A>C
n.859A>C
6g.156778705A>GCA366382848ARID1Bc.1025A>G (p.Gln342Arg)
c.776A>G (p.Gln259Arg)
c.765A>G
n.859A>G
ClinVar dbSNP gnomAD v4
6g.156778705A>TCA366382849ARID1Bc.1025A>T (p.Gln342Leu)
c.776A>T (p.Gln259Leu)
c.765A>T
n.859A>T
6g.156778707delCA2680909100ARID1Bc.1027del (p.Ser343AlafsTer6)
c.778del (p.Ser260AlafsTer6)
c.767del
n.861del
gnomAD v4
6g.156778706A>CCA366382852ARID1Bc.1026A>C (p.Gln342His)
c.777A>C (p.Gln259His)
c.766A>C
n.860A>C
gnomAD v4
6g.156778706A>GCA452989095ARID1Bc.1026A>G (p.Gln342=)
c.777A>G (p.Gln259=)
c.766A>G
n.860A>G
gnomAD v4
6g.156778706A>TCA366382853ARID1Bc.1026A>T (p.Gln342His)
c.777A>T (p.Gln259His)
c.766A>T
n.860A>T
6g.156778707A>CCA366382854ARID1Bc.1027A>C (p.Ser343Arg)
c.778A>C (p.Ser260Arg)
c.767A>C
n.861A>C
6g.156778707A>GCA366382855ARID1Bc.1027A>G (p.Ser343Gly)
c.778A>G (p.Ser260Gly)
c.767A>G
n.861A>G
dbSNP gnomAD v4
6g.156778707A>TCA366382857ARID1Bc.1027A>T (p.Ser343Cys)
c.778A>T (p.Ser260Cys)
c.767A>T
n.861A>T
6g.156778708G>ACA366382859ARID1Bc.1028G>A (p.Ser343Asn)
c.779G>A (p.Ser260Asn)
c.768G>A
n.862G>A
dbSNP gnomAD v4
6g.156778708G>CCA366382861ARID1Bc.1028G>C (p.Ser343Thr)
c.779G>C (p.Ser260Thr)
c.768G>C
n.862G>C
6g.156778708G=CA1675343679ARID1Bc.1028G= (p.Ser343=)
c.779G= (p.Ser260=)
c.768G=
n.862G=
6g.156778708G>TCA366382863ARID1Bc.1028G>T (p.Ser343Ile)
c.779G>T (p.Ser260Ile)
c.768G>T
n.862G>T
6g.156778709C>ACA150802752ARID1Bc.1029C>A (p.Ser343Arg)
c.780C>A (p.Ser260Arg)
c.769C>A
n.863C>A
dbSNP gnomAD v4
6g.156778709C=CA1675343680ARID1Bc.1029C= (p.Ser343=)
c.780C= (p.Ser260=)
c.769C=
n.863C=
6g.156778709C>GCA366382865ARID1Bc.1029C>G (p.Ser343Arg)
c.780C>G (p.Ser260Arg)
c.769C>G
n.863C>G
dbSNP gnomAD v4
6g.156778709C>TCA452989106ARID1Bc.1029C>T (p.Ser343=)
c.780C>T (p.Ser260=)
c.769C>T
n.863C>T
dbSNP gnomAD v2 gnomAD v4
6g.156778712delCA2680909101ARID1Bc.1032del (p.Met346TrpfsTer3)
c.783del (p.Met263TrpfsTer3)
c.772del
n.866del
gnomAD v4
6g.156778710C>ACA366382867ARID1Bc.1030C>A (p.Pro344Thr)
c.781C>A (p.Pro261Thr)
c.770C>A
n.864C>A
dbSNP
6g.156778710C>GCA366382869ARID1Bc.1030C>G (p.Pro344Ala)
c.781C>G (p.Pro261Ala)
c.770C>G
n.864C>G
gnomAD v4
6g.156778710C>TCA366382870ARID1Bc.1030C>T (p.Pro344Ser)
c.781C>T (p.Pro261Ser)
c.770C>T
n.864C>T
gnomAD v4
6g.156778711C>ACA366382875ARID1Bc.1031C>A (p.Pro344His)
c.782C>A (p.Pro261His)
c.771C>A
n.865C>A
dbSNP gnomAD v4
6g.156778711C=CA1675343681ARID1Bc.1031C= (p.Pro344=)
c.782C= (p.Pro261=)
c.771C=
n.865C=

Number of alleles fetched