Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.156778665_156778763del | CA2680909077 | ARID1B | c.985_1083del (p.Gly329_Gly361del) c.736_834del (p.Gly246_Gly278del) c.725_823del n.819_917del | gnomAD v4 |
6 | g.156778698G>A | CA366382814 | ARID1B | c.1018G>A (p.Gly340Arg) c.769G>A (p.Gly257Arg) c.758G>A n.852G>A | gnomAD v4 |
6 | g.156778698G>C | CA366382816 | ARID1B | c.1018G>C (p.Gly340Arg) c.769G>C (p.Gly257Arg) c.758G>C n.852G>C | |
6 | g.156778698G= | CA1675343676 | ARID1B | c.1018G= (p.Gly340=) c.769G= (p.Gly257=) c.758G= n.852G= | |
6 | g.156778698G>T | CA16042552 | ARID1B | c.1018G>T (p.Gly340Ter) c.769G>T (p.Gly257Ter) c.758G>T n.852G>T | ClinVar dbSNP gnomAD v4 |
6 | g.156778699del | CA2680909098 | ARID1B | c.1019del (p.Gly340AspfsTer9) c.770del (p.Gly257AspfsTer9) c.759del n.853del | gnomAD v4 |
6 | g.156778699G>A | CA366382820 | ARID1B | c.1019G>A (p.Gly340Glu) c.770G>A (p.Gly257Glu) c.759G>A n.853G>A | dbSNP gnomAD v4 |
6 | g.156778699G>C | CA366382819 | ARID1B | c.1019G>C (p.Gly340Ala) c.770G>C (p.Gly257Ala) c.759G>C n.853G>C | |
6 | g.156778699G= | CA1675343677 | ARID1B | c.1019G= (p.Gly340=) c.770G= (p.Gly257=) c.759G= n.853G= | |
6 | g.156778699G>T | CA366382822 | ARID1B | c.1019G>T (p.Gly340Val) c.770G>T (p.Gly257Val) c.759G>T n.853G>T | dbSNP gnomAD v4 |
6 | g.156778700A>C | CA452989073 | ARID1B | c.1020A>C (p.Gly340=) c.771A>C (p.Gly257=) c.760A>C n.854A>C | dbSNP |
6 | g.156778700A>G | CA452989076 | ARID1B | c.1020A>G (p.Gly340=) c.771A>G (p.Gly257=) c.760A>G n.854A>G | dbSNP gnomAD v4 |
6 | g.156778700A>T | CA452989079 | ARID1B | c.1020A>T (p.Gly340=) c.771A>T (p.Gly257=) c.760A>T n.854A>T | |
6 | g.156778701C>A | CA366382824 | ARID1B | c.1021C>A (p.Gln341Lys) c.772C>A (p.Gln258Lys) c.761C>A n.855C>A | |
6 | g.156778701C= | CA1675343678 | ARID1B | c.1021C= (p.Gln341=) c.772C= (p.Gln258=) c.761C= n.855C= | |
6 | g.156778701C>G | CA366382826 | ARID1B | c.1021C>G (p.Gln341Glu) c.772C>G (p.Gln258Glu) c.761C>G n.855C>G | dbSNP gnomAD v4 |
6 | g.156778701C>T | CA366382827 | ARID1B | c.1021C>T (p.Gln341Ter) c.772C>T (p.Gln258Ter) c.761C>T n.855C>T | ClinVar gnomAD v4 |
6 | g.156778702A>C | CA366382830 | ARID1B | c.1022A>C (p.Gln341Pro) c.773A>C (p.Gln258Pro) c.762A>C n.856A>C | gnomAD v4 |
6 | g.156778702A>G | CA366382832 | ARID1B | c.1022A>G (p.Gln341Arg) c.773A>G (p.Gln258Arg) c.762A>G n.856A>G | |
6 | g.156778702A>T | CA366382833 | ARID1B | c.1022A>T (p.Gln341Leu) c.773A>T (p.Gln258Leu) c.762A>T n.856A>T | |
6 | g.156778703A>C | CA366382836 | ARID1B | c.1023A>C (p.Gln341His) c.774A>C (p.Gln258His) c.763A>C n.857A>C | |
6 | g.156778703A>G | CA452989087 | ARID1B | c.1023A>G (p.Gln341=) c.774A>G (p.Gln258=) c.763A>G n.857A>G | gnomAD v4 |
6 | g.156778703A>T | CA366382838 | ARID1B | c.1023A>T (p.Gln341His) c.774A>T (p.Gln258His) c.763A>T n.857A>T | |
6 | g.156778704C>A | CA366382840 | ARID1B | c.1024C>A (p.Gln342Lys) c.775C>A (p.Gln259Lys) c.764C>A n.858C>A | gnomAD v4 |
6 | g.156778704C>G | CA366382842 | ARID1B | c.1024C>G (p.Gln342Glu) c.775C>G (p.Gln259Glu) c.764C>G n.858C>G | gnomAD v4 |
6 | g.156778704C>T | CA366382843 | ARID1B | c.1024C>T (p.Gln342Ter) c.775C>T (p.Gln259Ter) c.764C>T n.858C>T | gnomAD v4 |
6 | g.156778705A>C | CA366382846 | ARID1B | c.1025A>C (p.Gln342Pro) c.776A>C (p.Gln259Pro) c.765A>C n.859A>C | |
6 | g.156778705A>G | CA366382848 | ARID1B | c.1025A>G (p.Gln342Arg) c.776A>G (p.Gln259Arg) c.765A>G n.859A>G | ClinVar dbSNP gnomAD v4 |
6 | g.156778705A>T | CA366382849 | ARID1B | c.1025A>T (p.Gln342Leu) c.776A>T (p.Gln259Leu) c.765A>T n.859A>T | |
6 | g.156778707del | CA2680909100 | ARID1B | c.1027del (p.Ser343AlafsTer6) c.778del (p.Ser260AlafsTer6) c.767del n.861del | gnomAD v4 |
6 | g.156778706A>C | CA366382852 | ARID1B | c.1026A>C (p.Gln342His) c.777A>C (p.Gln259His) c.766A>C n.860A>C | gnomAD v4 |
6 | g.156778706A>G | CA452989095 | ARID1B | c.1026A>G (p.Gln342=) c.777A>G (p.Gln259=) c.766A>G n.860A>G | gnomAD v4 |
6 | g.156778706A>T | CA366382853 | ARID1B | c.1026A>T (p.Gln342His) c.777A>T (p.Gln259His) c.766A>T n.860A>T | |
6 | g.156778707A>C | CA366382854 | ARID1B | c.1027A>C (p.Ser343Arg) c.778A>C (p.Ser260Arg) c.767A>C n.861A>C | |
6 | g.156778707A>G | CA366382855 | ARID1B | c.1027A>G (p.Ser343Gly) c.778A>G (p.Ser260Gly) c.767A>G n.861A>G | dbSNP gnomAD v4 |
6 | g.156778707A>T | CA366382857 | ARID1B | c.1027A>T (p.Ser343Cys) c.778A>T (p.Ser260Cys) c.767A>T n.861A>T | |
6 | g.156778708G>A | CA366382859 | ARID1B | c.1028G>A (p.Ser343Asn) c.779G>A (p.Ser260Asn) c.768G>A n.862G>A | dbSNP gnomAD v4 |
6 | g.156778708G>C | CA366382861 | ARID1B | c.1028G>C (p.Ser343Thr) c.779G>C (p.Ser260Thr) c.768G>C n.862G>C | |
6 | g.156778708G= | CA1675343679 | ARID1B | c.1028G= (p.Ser343=) c.779G= (p.Ser260=) c.768G= n.862G= | |
6 | g.156778708G>T | CA366382863 | ARID1B | c.1028G>T (p.Ser343Ile) c.779G>T (p.Ser260Ile) c.768G>T n.862G>T | |
6 | g.156778709C>A | CA150802752 | ARID1B | c.1029C>A (p.Ser343Arg) c.780C>A (p.Ser260Arg) c.769C>A n.863C>A | dbSNP gnomAD v4 |
6 | g.156778709C= | CA1675343680 | ARID1B | c.1029C= (p.Ser343=) c.780C= (p.Ser260=) c.769C= n.863C= | |
6 | g.156778709C>G | CA366382865 | ARID1B | c.1029C>G (p.Ser343Arg) c.780C>G (p.Ser260Arg) c.769C>G n.863C>G | dbSNP gnomAD v4 |
6 | g.156778709C>T | CA452989106 | ARID1B | c.1029C>T (p.Ser343=) c.780C>T (p.Ser260=) c.769C>T n.863C>T | dbSNP gnomAD v2 gnomAD v4 |
6 | g.156778712del | CA2680909101 | ARID1B | c.1032del (p.Met346TrpfsTer3) c.783del (p.Met263TrpfsTer3) c.772del n.866del | gnomAD v4 |
6 | g.156778710C>A | CA366382867 | ARID1B | c.1030C>A (p.Pro344Thr) c.781C>A (p.Pro261Thr) c.770C>A n.864C>A | dbSNP |
6 | g.156778710C>G | CA366382869 | ARID1B | c.1030C>G (p.Pro344Ala) c.781C>G (p.Pro261Ala) c.770C>G n.864C>G | gnomAD v4 |
6 | g.156778710C>T | CA366382870 | ARID1B | c.1030C>T (p.Pro344Ser) c.781C>T (p.Pro261Ser) c.770C>T n.864C>T | gnomAD v4 |
6 | g.156778711C>A | CA366382875 | ARID1B | c.1031C>A (p.Pro344His) c.782C>A (p.Pro261His) c.771C>A n.865C>A | dbSNP gnomAD v4 |
6 | g.156778711C= | CA1675343681 | ARID1B | c.1031C= (p.Pro344=) c.782C= (p.Pro261=) c.771C= n.865C= |