Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.45852522_45852540delCA645571097ARID2c.4399_4417del (p.Val1467LeufsTer12)
c.608_626del
c.4320_4338del
c.3952_3970del (p.Val1318LeufsTer12)
c.3229_3247del (p.Val1077LeufsTer12)
c.223_241del (p.Val75LeufsTer12)
n.3690_3708del
c.2767_2785del (p.Val923LeufsTer12)
n.4547_4565del
n.4530_4548del
COSMIC
12g.45852539_45852545delCA645571098ARID2c.4416_4422del (p.His1472GlnfsTer11)
c.625_631del
c.4337_4343del
c.3969_3975del (p.His1323GlnfsTer11)
c.3246_3252del (p.His1082GlnfsTer11)
c.240_246del (p.His80GlnfsTer11)
n.3707_3713del
c.2784_2790del (p.His928GlnfsTer11)
n.4564_4570del
n.4547_4553del
COSMIC
12g.45852539T>ACA384491567ARID2c.4416T>A (p.His1472Gln)
c.625T>A
c.4337T>A
c.3969T>A (p.His1323Gln)
c.3246T>A (p.His1082Gln)
c.240T>A (p.His80Gln)
n.3707T>A
c.2784T>A (p.His928Gln)
n.4564T>A
n.4547T>A
12g.45852539T>CCA479693803ARID2c.4416T>C (p.His1472=)
c.625T>C
c.4337T>C
c.3969T>C (p.His1323=)
c.3246T>C (p.His1082=)
c.240T>C (p.His80=)
n.3707T>C
c.2784T>C (p.His928=)
n.4564T>C
n.4547T>C
12g.45852539T>GCA384491569ARID2c.4416T>G (p.His1472Gln)
c.625T>G
c.4337T>G
c.3969T>G (p.His1323Gln)
c.3246T>G (p.His1082Gln)
c.240T>G (p.His80Gln)
n.3707T>G
c.2784T>G (p.His928Gln)
n.4564T>G
n.4547T>G
gnomAD v4
12g.45852540T>ACA384491572ARID2c.4417T>A (p.Ser1473Thr)
c.626T>A
c.4338T>A
c.3970T>A (p.Ser1324Thr)
c.3247T>A (p.Ser1083Thr)
c.241T>A (p.Ser81Thr)
n.3708T>A
c.2785T>A (p.Ser929Thr)
n.4565T>A
n.4548T>A
dbSNP
12g.45852540T>CCA384491574ARID2c.4417T>C (p.Ser1473Pro)
c.626T>C
c.4338T>C
c.3970T>C (p.Ser1324Pro)
c.3247T>C (p.Ser1083Pro)
c.241T>C (p.Ser81Pro)
n.3708T>C
c.2785T>C (p.Ser929Pro)
n.4565T>C
n.4548T>C
dbSNP
12g.45852540T>GCA384491575ARID2c.4417T>G (p.Ser1473Ala)
c.626T>G
c.4338T>G
c.3970T>G (p.Ser1324Ala)
c.3247T>G (p.Ser1083Ala)
c.241T>G (p.Ser81Ala)
n.3708T>G
c.2785T>G (p.Ser929Ala)
n.4565T>G
n.4548T>G
12g.45852541C>ACA384491579ARID2c.4418C>A (p.Ser1473Tyr)
c.627C>A
c.4339C>A
c.3971C>A (p.Ser1324Tyr)
c.3248C>A (p.Ser1083Tyr)
c.242C>A (p.Ser81Tyr)
n.3709C>A
c.2786C>A (p.Ser929Tyr)
n.4566C>A
n.4549C>A
dbSNP
12g.45852541C=CA2033475658ARID2c.4418C= (p.Ser1473=)
c.627C=
c.4339C=
c.3971C= (p.Ser1324=)
c.3248C= (p.Ser1083=)
c.242C= (p.Ser81=)
n.3709C=
c.2786C= (p.Ser929=)
n.4566C=
n.4549C=
12g.45852541C>GCA384491581ARID2c.4418C>G (p.Ser1473Cys)
c.627C>G
c.4339C>G
c.3971C>G (p.Ser1324Cys)
c.3248C>G (p.Ser1083Cys)
c.242C>G (p.Ser81Cys)
n.3709C>G
c.2786C>G (p.Ser929Cys)
n.4566C>G
n.4549C>G
dbSNP gnomAD v4
12g.45852541C>TCA6526656ARID2c.4418C>T (p.Ser1473Phe)
c.627C>T
c.4339C>T
c.3971C>T (p.Ser1324Phe)
c.3248C>T (p.Ser1083Phe)
c.242C>T (p.Ser81Phe)
n.3709C>T
c.2786C>T (p.Ser929Phe)
n.4566C>T
n.4549C>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852542T>ACA479693804ARID2c.4419T>A (p.Ser1473=)
c.628T>A
c.4340T>A
c.3972T>A (p.Ser1324=)
c.3249T>A (p.Ser1083=)
c.243T>A (p.Ser81=)
n.3710T>A
c.2787T>A (p.Ser929=)
n.4567T>A
n.4550T>A
12g.45852542T>CCA479693805ARID2c.4419T>C (p.Ser1473=)
c.628T>C
c.4340T>C
c.3972T>C (p.Ser1324=)
c.3249T>C (p.Ser1083=)
c.243T>C (p.Ser81=)
n.3710T>C
c.2787T>C (p.Ser929=)
n.4567T>C
n.4550T>C
12g.45852542T>GCA479693806ARID2c.4419T>G (p.Ser1473=)
c.628T>G
c.4340T>G
c.3972T>G (p.Ser1324=)
c.3249T>G (p.Ser1083=)
c.243T>G (p.Ser81=)
n.3710T>G
c.2787T>G (p.Ser929=)
n.4567T>G
n.4550T>G
12g.45852543A=CA2033475659ARID2c.4420A= (p.Thr1474=)
c.629A=
c.4341A=
c.3973A= (p.Thr1325=)
c.3250A= (p.Thr1084=)
c.244A= (p.Thr82=)
n.3711A=
c.2788A= (p.Thr930=)
n.4568A=
n.4551A=
12g.45852543A>CCA384491586ARID2c.4420A>C (p.Thr1474Pro)
c.629A>C
c.4341A>C
c.3973A>C (p.Thr1325Pro)
c.3250A>C (p.Thr1084Pro)
c.244A>C (p.Thr82Pro)
n.3711A>C
c.2788A>C (p.Thr930Pro)
n.4568A>C
n.4551A>C
dbSNP gnomAD v2
12g.45852543A>GCA384491587ARID2c.4420A>G (p.Thr1474Ala)
c.629A>G
c.4341A>G
c.3973A>G (p.Thr1325Ala)
c.3250A>G (p.Thr1084Ala)
c.244A>G (p.Thr82Ala)
n.3711A>G
c.2788A>G (p.Thr930Ala)
n.4568A>G
n.4551A>G
ClinVar dbSNP gnomAD v4
12g.45852543A>TCA384491589ARID2c.4420A>T (p.Thr1474Ser)
c.629A>T
c.4341A>T
c.3973A>T (p.Thr1325Ser)
c.3250A>T (p.Thr1084Ser)
c.244A>T (p.Thr82Ser)
n.3711A>T
c.2788A>T (p.Thr930Ser)
n.4568A>T
n.4551A>T
dbSNP
12g.45852544C>ACA384491592ARID2c.4421C>A (p.Thr1474Lys)
c.630C>A
c.4342C>A
c.3974C>A (p.Thr1325Lys)
c.3251C>A (p.Thr1084Lys)
c.245C>A (p.Thr82Lys)
n.3712C>A
c.2789C>A (p.Thr930Lys)
n.4569C>A
n.4552C>A
dbSNP
12g.45852544C>GCA384491594ARID2c.4421C>G (p.Thr1474Arg)
c.630C>G
c.4342C>G
c.3974C>G (p.Thr1325Arg)
c.3251C>G (p.Thr1084Arg)
c.245C>G (p.Thr82Arg)
n.3712C>G
c.2789C>G (p.Thr930Arg)
n.4569C>G
n.4552C>G
dbSNP
12g.45852544C>TCA384491597ARID2c.4421C>T (p.Thr1474Ile)
c.630C>T
c.4342C>T
c.3974C>T (p.Thr1325Ile)
c.3251C>T (p.Thr1084Ile)
c.245C>T (p.Thr82Ile)
n.3712C>T
c.2789C>T (p.Thr930Ile)
n.4569C>T
n.4552C>T
dbSNP
12g.45852545A=CA2033475660ARID2c.4422A= (p.Thr1474=)
c.631A=
c.4343A=
c.3975A= (p.Thr1325=)
c.3252A= (p.Thr1084=)
c.246A= (p.Thr82=)
n.3713A=
c.2790A= (p.Thr930=)
n.4570A=
n.4553A=
12g.45852545A>CCA479693807ARID2c.4422A>C (p.Thr1474=)
c.631A>C
c.4343A>C
c.3975A>C (p.Thr1325=)
c.3252A>C (p.Thr1084=)
c.246A>C (p.Thr82=)
n.3713A>C
c.2790A>C (p.Thr930=)
n.4570A>C
n.4553A>C
12g.45852545A>GCA479693808ARID2c.4422A>G (p.Thr1474=)
c.631A>G
c.4343A>G
c.3975A>G (p.Thr1325=)
c.3252A>G (p.Thr1084=)
c.246A>G (p.Thr82=)
n.3713A>G
c.2790A>G (p.Thr930=)
n.4570A>G
n.4553A>G
dbSNP gnomAD v2 gnomAD v4
12g.45852545A>TCA479693809ARID2c.4422A>T (p.Thr1474=)
c.631A>T
c.4343A>T
c.3975A>T (p.Thr1325=)
c.3252A>T (p.Thr1084=)
c.246A>T (p.Thr82=)
n.3713A>T
c.2790A>T (p.Thr930=)
n.4570A>T
n.4553A>T
dbSNP
12g.45852546A>CCA384491602ARID2c.4423A>C (p.Thr1475Pro)
c.632A>C
c.4344A>C
c.3976A>C (p.Thr1326Pro)
c.3253A>C (p.Thr1085Pro)
c.247A>C (p.Thr83Pro)
n.3714A>C
c.2791A>C (p.Thr931Pro)
n.4571A>C
n.4554A>C
dbSNP
12g.45852546A>GCA384491598ARID2c.4423A>G (p.Thr1475Ala)
c.632A>G
c.4344A>G
c.3976A>G (p.Thr1326Ala)
c.3253A>G (p.Thr1085Ala)
c.247A>G (p.Thr83Ala)
n.3714A>G
c.2791A>G (p.Thr931Ala)
n.4571A>G
n.4554A>G
dbSNP
12g.45852546A>TCA384491600ARID2c.4423A>T (p.Thr1475Ser)
c.632A>T
c.4344A>T
c.3976A>T (p.Thr1326Ser)
c.3253A>T (p.Thr1085Ser)
c.247A>T (p.Thr83Ser)
n.3714A>T
c.2791A>T (p.Thr931Ser)
n.4571A>T
n.4554A>T
dbSNP
12g.45852547C>ACA384491606ARID2c.4424C>A (p.Thr1475Asn)
c.633C>A
c.4345C>A
c.3977C>A (p.Thr1326Asn)
c.3254C>A (p.Thr1085Asn)
c.248C>A (p.Thr83Asn)
n.3715C>A
c.2792C>A (p.Thr931Asn)
n.4572C>A
n.4555C>A
dbSNP
12g.45852547C=CA2033475661ARID2c.4424C= (p.Thr1475=)
c.633C=
c.4345C=
c.3977C= (p.Thr1326=)
c.3254C= (p.Thr1085=)
c.248C= (p.Thr83=)
n.3715C=
c.2792C= (p.Thr931=)
n.4572C=
n.4555C=
12g.45852547C>GCA384491608ARID2c.4424C>G (p.Thr1475Ser)
c.633C>G
c.4345C>G
c.3977C>G (p.Thr1326Ser)
c.3254C>G (p.Thr1085Ser)
c.248C>G (p.Thr83Ser)
n.3715C>G
c.2792C>G (p.Thr931Ser)
n.4572C>G
n.4555C>G
dbSNP
12g.45852547C>TCA384491609ARID2c.4424C>T (p.Thr1475Ile)
c.633C>T
c.4345C>T
c.3977C>T (p.Thr1326Ile)
c.3254C>T (p.Thr1085Ile)
c.248C>T (p.Thr83Ile)
n.3715C>T
c.2792C>T (p.Thr931Ile)
n.4572C>T
n.4555C>T
dbSNP gnomAD v2 gnomAD v4
12g.45852548C>ACA479693810ARID2c.4425C>A (p.Thr1475=)
c.634C>A
c.4346C>A
c.3978C>A (p.Thr1326=)
c.3255C>A (p.Thr1085=)
c.249C>A (p.Thr83=)
n.3716C>A
c.2793C>A (p.Thr931=)
n.4573C>A
n.4556C>A
dbSNP
12g.45852548C=CA2033475662ARID2c.4425C= (p.Thr1475=)
c.634C=
c.4346C=
c.3978C= (p.Thr1326=)
c.3255C= (p.Thr1085=)
c.249C= (p.Thr83=)
n.3716C=
c.2793C= (p.Thr931=)
n.4573C=
n.4556C=
12g.45852548C>GCA479693811ARID2c.4425C>G (p.Thr1475=)
c.634C>G
c.4346C>G
c.3978C>G (p.Thr1326=)
c.3255C>G (p.Thr1085=)
c.249C>G (p.Thr83=)
n.3716C>G
c.2793C>G (p.Thr931=)
n.4573C>G
n.4556C>G
12g.45852548C>TCA479693812ARID2c.4425C>T (p.Thr1475=)
c.634C>T
c.4346C>T
c.3978C>T (p.Thr1326=)
c.3255C>T (p.Thr1085=)
c.249C>T (p.Thr83=)
n.3716C>T
c.2793C>T (p.Thr931=)
n.4573C>T
n.4556C>T
gnomAD v4 COSMIC
12g.45852549T>ACA384491612ARID2c.4426T>A (p.Ser1476Thr)
c.635T>A
c.4347T>A
c.3979T>A (p.Ser1327Thr)
c.3256T>A (p.Ser1086Thr)
c.250T>A (p.Ser84Thr)
n.3717T>A
c.2794T>A (p.Ser932Thr)
n.4574T>A
n.4557T>A
dbSNP
12g.45852549T>CCA384491615ARID2c.4426T>C (p.Ser1476Pro)
c.635T>C
c.4347T>C
c.3979T>C (p.Ser1327Pro)
c.3256T>C (p.Ser1086Pro)
c.250T>C (p.Ser84Pro)
n.3717T>C
c.2794T>C (p.Ser932Pro)
n.4574T>C
n.4557T>C
dbSNP
12g.45852549T>GCA384491617ARID2c.4426T>G (p.Ser1476Ala)
c.635T>G
c.4347T>G
c.3979T>G (p.Ser1327Ala)
c.3256T>G (p.Ser1086Ala)
c.250T>G (p.Ser84Ala)
n.3717T>G
c.2794T>G (p.Ser932Ala)
n.4574T>G
n.4557T>G
12g.45852550C>ACA384491623ARID2c.4427C>A (p.Ser1476Tyr)
c.636C>A
c.4348C>A
c.3980C>A (p.Ser1327Tyr)
c.3257C>A (p.Ser1086Tyr)
c.251C>A (p.Ser84Tyr)
n.3718C>A
c.2795C>A (p.Ser932Tyr)
n.4575C>A
n.4558C>A
12g.45852550C=CA2033475663ARID2c.4427C= (p.Ser1476=)
c.636C=
c.4348C=
c.3980C= (p.Ser1327=)
c.3257C= (p.Ser1086=)
c.251C= (p.Ser84=)
n.3718C=
c.2795C= (p.Ser932=)
n.4575C=
n.4558C=
12g.45852550C>GCA236400699ARID2c.4427C>G (p.Ser1476Cys)
c.636C>G
c.4348C>G
c.3980C>G (p.Ser1327Cys)
c.3257C>G (p.Ser1086Cys)
c.251C>G (p.Ser84Cys)
n.3718C>G
c.2795C>G (p.Ser932Cys)
n.4575C>G
n.4558C>G
dbSNP gnomAD v4
12g.45852550C>TCA384491620ARID2c.4427C>T (p.Ser1476Phe)
c.636C>T
c.4348C>T
c.3980C>T (p.Ser1327Phe)
c.3257C>T (p.Ser1086Phe)
c.251C>T (p.Ser84Phe)
n.3718C>T
c.2795C>T (p.Ser932Phe)
n.4575C>T
n.4558C>T
COSMIC
12g.45852551T>ACA479693814ARID2c.4428T>A (p.Ser1476=)
c.637T>A
c.4349T>A
c.3981T>A (p.Ser1327=)
c.3258T>A (p.Ser1086=)
c.252T>A (p.Ser84=)
n.3719T>A
c.2796T>A (p.Ser932=)
n.4576T>A
n.4559T>A
dbSNP
12g.45852551T>CCA6526657ARID2c.4428T>C (p.Ser1476=)
c.637T>C
c.4349T>C
c.3981T>C (p.Ser1327=)
c.3258T>C (p.Ser1086=)
c.252T>C (p.Ser84=)
n.3719T>C
c.2796T>C (p.Ser932=)
n.4576T>C
n.4559T>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852551T>GCA479693815ARID2c.4428T>G (p.Ser1476=)
c.637T>G
c.4349T>G
c.3981T>G (p.Ser1327=)
c.3258T>G (p.Ser1086=)
c.252T>G (p.Ser84=)
n.3719T>G
c.2796T>G (p.Ser932=)
n.4576T>G
n.4559T>G
12g.45852551T=CA2033475664ARID2c.4428T= (p.Ser1476=)
c.637T=
c.4349T=
c.3981T= (p.Ser1327=)
c.3258T= (p.Ser1086=)
c.252T= (p.Ser84=)
n.3719T=
c.2796T= (p.Ser932=)
n.4576T=
n.4559T=
12g.45852551dupCA479693813ARID2c.4428dup (p.Val1477CysfsTer26)
c.637dup
c.4349dup
c.3981dup (p.Val1328CysfsTer26)
c.3258dup (p.Val1087CysfsTer26)
c.252dup (p.Val85CysfsTer26)
n.3719dup
c.2796dup (p.Val933CysfsTer26)
n.4576dup
n.4559dup
COSMIC
12g.45852552G>ACA384491629ARID2c.4429G>A (p.Val1477Ile)
c.638G>A
c.4350G>A
c.3982G>A (p.Val1328Ile)
c.3259G>A (p.Val1087Ile)
c.253G>A (p.Val85Ile)
n.3720G>A
c.2797G>A (p.Val933Ile)
n.4577G>A
n.4560G>A
dbSNP
12g.45852552G>CCA384491631ARID2c.4429G>C (p.Val1477Leu)
c.638G>C
c.4350G>C
c.3982G>C (p.Val1328Leu)
c.3259G>C (p.Val1087Leu)
c.253G>C (p.Val85Leu)
n.3720G>C
c.2797G>C (p.Val933Leu)
n.4577G>C
n.4560G>C
dbSNP
12g.45852552G>TCA384491633ARID2c.4429G>T (p.Val1477Phe)
c.638G>T
c.4350G>T
c.3982G>T (p.Val1328Phe)
c.3259G>T (p.Val1087Phe)
c.253G>T (p.Val85Phe)
n.3720G>T
c.2797G>T (p.Val933Phe)
n.4577G>T
n.4560G>T
dbSNP
12g.45852553T>ACA384491637ARID2c.4430T>A (p.Val1477Asp)
c.639T>A
c.4351T>A
c.3983T>A (p.Val1328Asp)
c.3260T>A (p.Val1087Asp)
c.254T>A (p.Val85Asp)
n.3721T>A
c.2798T>A (p.Val933Asp)
n.4578T>A
n.4561T>A
12g.45852553T>CCA384491639ARID2c.4430T>C (p.Val1477Ala)
c.639T>C
c.4351T>C
c.3983T>C (p.Val1328Ala)
c.3260T>C (p.Val1087Ala)
c.254T>C (p.Val85Ala)
n.3721T>C
c.2798T>C (p.Val933Ala)
n.4578T>C
n.4561T>C
dbSNP
12g.45852553T>GCA384491641ARID2c.4430T>G (p.Val1477Gly)
c.639T>G
c.4351T>G
c.3983T>G (p.Val1328Gly)
c.3260T>G (p.Val1087Gly)
c.254T>G (p.Val85Gly)
n.3721T>G
c.2798T>G (p.Val933Gly)
n.4578T>G
n.4561T>G
12g.45852553T=CA2033475665ARID2c.4430T= (p.Val1477=)
c.639T=
c.4351T=
c.3983T= (p.Val1328=)
c.3260T= (p.Val1087=)
c.254T= (p.Val85=)
n.3721T=
c.2798T= (p.Val933=)
n.4578T=
n.4561T=
12g.45852554T>ACA479693816ARID2c.4431T>A (p.Val1477=)
c.640T>A
c.4352T>A
c.3984T>A (p.Val1328=)
c.3261T>A (p.Val1087=)
c.255T>A (p.Val85=)
n.3722T>A
c.2799T>A (p.Val933=)
n.4579T>A
n.4562T>A
dbSNP
12g.45852554T>CCA479693817ARID2c.4431T>C (p.Val1477=)
c.640T>C
c.4352T>C
c.3984T>C (p.Val1328=)
c.3261T>C (p.Val1087=)
c.255T>C (p.Val85=)
n.3722T>C
c.2799T>C (p.Val933=)
n.4579T>C
n.4562T>C
dbSNP gnomAD v4
12g.45852554T>GCA479693818ARID2c.4431T>G (p.Val1477=)
c.640T>G
c.4352T>G
c.3984T>G (p.Val1328=)
c.3261T>G (p.Val1087=)
c.255T>G (p.Val85=)
n.3722T>G
c.2799T>G (p.Val933=)
n.4579T>G
n.4562T>G
12g.45852554T=CA2033475666ARID2c.4431T= (p.Val1477=)
c.640T=
c.4352T=
c.3984T= (p.Val1328=)
c.3261T= (p.Val1087=)
c.255T= (p.Val85=)
n.3722T=
c.2799T= (p.Val933=)
n.4579T=
n.4562T=
12g.45852555A=CA2033475667ARID2c.4432A= (p.Ile1478=)
c.641A=
c.4353A=
c.3985A= (p.Ile1329=)
c.3262A= (p.Ile1088=)
c.256A= (p.Ile86=)
n.3723A=
c.2800A= (p.Ile934=)
n.4580A=
n.4563A=
12g.45852555A>CCA384491644ARID2c.4432A>C (p.Ile1478Leu)
c.641A>C
c.4353A>C
c.3985A>C (p.Ile1329Leu)
c.3262A>C (p.Ile1088Leu)
c.256A>C (p.Ile86Leu)
n.3723A>C
c.2800A>C (p.Ile934Leu)
n.4580A>C
n.4563A>C
12g.45852555A>GCA6526658ARID2c.4432A>G (p.Ile1478Val)
c.641A>G
c.4353A>G
c.3985A>G (p.Ile1329Val)
c.3262A>G (p.Ile1088Val)
c.256A>G (p.Ile86Val)
n.3723A>G
c.2800A>G (p.Ile934Val)
n.4580A>G
n.4563A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852555A>TCA384491646ARID2c.4432A>T (p.Ile1478Leu)
c.641A>T
c.4353A>T
c.3985A>T (p.Ile1329Leu)
c.3262A>T (p.Ile1088Leu)
c.256A>T (p.Ile86Leu)
n.3723A>T
c.2800A>T (p.Ile934Leu)
n.4580A>T
n.4563A>T
dbSNP
12g.45852556T>ACA384491650ARID2c.4433T>A (p.Ile1478Lys)
c.642T>A
c.4354T>A
c.3986T>A (p.Ile1329Lys)
c.3263T>A (p.Ile1088Lys)
c.257T>A (p.Ile86Lys)
n.3724T>A
c.2801T>A (p.Ile934Lys)
n.4581T>A
n.4564T>A
dbSNP
12g.45852556T>CCA6526659ARID2c.4433T>C (p.Ile1478Thr)
c.642T>C
c.4354T>C
c.3986T>C (p.Ile1329Thr)
c.3263T>C (p.Ile1088Thr)
c.257T>C (p.Ile86Thr)
n.3724T>C
c.2801T>C (p.Ile934Thr)
n.4581T>C
n.4564T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852556T>GCA384491653ARID2c.4433T>G (p.Ile1478Arg)
c.642T>G
c.4354T>G
c.3986T>G (p.Ile1329Arg)
c.3263T>G (p.Ile1088Arg)
c.257T>G (p.Ile86Arg)
n.3724T>G
c.2801T>G (p.Ile934Arg)
n.4581T>G
n.4564T>G
12g.45852556T=CA2033475668ARID2c.4433T= (p.Ile1478=)
c.642T=
c.4354T=
c.3986T= (p.Ile1329=)
c.3263T= (p.Ile1088=)
c.257T= (p.Ile86=)
n.3724T=
c.2801T= (p.Ile934=)
n.4581T=
n.4564T=
12g.45852557A>CCA479693819ARID2c.4434A>C (p.Ile1478=)
c.643A>C
c.4355A>C
c.3987A>C (p.Ile1329=)
c.3264A>C (p.Ile1088=)
c.258A>C (p.Ile86=)
n.3725A>C
c.2802A>C (p.Ile934=)
n.4582A>C
n.4565A>C
dbSNP
12g.45852557A>GCA384491656ARID2c.4434A>G (p.Ile1478Met)
c.643A>G
c.4355A>G
c.3987A>G (p.Ile1329Met)
c.3264A>G (p.Ile1088Met)
c.258A>G (p.Ile86Met)
n.3725A>G
c.2802A>G (p.Ile934Met)
n.4582A>G
n.4565A>G
dbSNP
12g.45852557A>TCA479693820ARID2c.4434A>T (p.Ile1478=)
c.643A>T
c.4355A>T
c.3987A>T (p.Ile1329=)
c.3264A>T (p.Ile1088=)
c.258A>T (p.Ile86=)
n.3725A>T
c.2802A>T (p.Ile934=)
n.4582A>T
n.4565A>T
dbSNP
12g.45852558C>ACA384491659ARID2c.4435C>A (p.Gln1479Lys)
c.644C>A
c.4356C>A
c.3988C>A (p.Gln1330Lys)
c.3265C>A (p.Gln1089Lys)
c.259C>A (p.Gln87Lys)
n.3726C>A
c.2803C>A (p.Gln935Lys)
n.4583C>A
n.4566C>A
dbSNP
12g.45852558C>GCA384491661ARID2c.4435C>G (p.Gln1479Glu)
c.644C>G
c.4356C>G
c.3988C>G (p.Gln1330Glu)
c.3265C>G (p.Gln1089Glu)
c.259C>G (p.Gln87Glu)
n.3726C>G
c.2803C>G (p.Gln935Glu)
n.4583C>G
n.4566C>G
12g.45852558C>TCA384491663ARID2c.4435C>T (p.Gln1479Ter)
c.644C>T
c.4356C>T
c.3988C>T (p.Gln1330Ter)
c.3265C>T (p.Gln1089Ter)
c.259C>T (p.Gln87Ter)
n.3726C>T
c.2803C>T (p.Gln935Ter)
n.4583C>T
n.4566C>T
12g.45852559A>CCA384491665ARID2c.4436A>C (p.Gln1479Pro)
c.645A>C
c.4357A>C
c.3989A>C (p.Gln1330Pro)
c.3266A>C (p.Gln1089Pro)
c.260A>C (p.Gln87Pro)
n.3727A>C
c.2804A>C (p.Gln935Pro)
n.4584A>C
n.4567A>C
12g.45852559A>GCA384491668ARID2c.4436A>G (p.Gln1479Arg)
c.645A>G
c.4357A>G
c.3989A>G (p.Gln1330Arg)
c.3266A>G (p.Gln1089Arg)
c.260A>G (p.Gln87Arg)
n.3727A>G
c.2804A>G (p.Gln935Arg)
n.4584A>G
n.4567A>G
12g.45852559A>TCA384491670ARID2c.4436A>T (p.Gln1479Leu)
c.645A>T
c.4357A>T
c.3989A>T (p.Gln1330Leu)
c.3266A>T (p.Gln1089Leu)
c.260A>T (p.Gln87Leu)
n.3727A>T
c.2804A>T (p.Gln935Leu)
n.4584A>T
n.4567A>T
12g.45852560G>ACA479693821ARID2c.4437G>A (p.Gln1479=)
c.646G>A
c.4358G>A
c.3990G>A (p.Gln1330=)
c.3267G>A (p.Gln1089=)
c.261G>A (p.Gln87=)
n.3728G>A
c.2805G>A (p.Gln935=)
n.4585G>A
n.4568G>A
dbSNP
12g.45852560G>CCA384491672ARID2c.4437G>C (p.Gln1479His)
c.646G>C
c.4358G>C
c.3990G>C (p.Gln1330His)
c.3267G>C (p.Gln1089His)
c.261G>C (p.Gln87His)
n.3728G>C
c.2805G>C (p.Gln935His)
n.4585G>C
n.4568G>C
dbSNP
12g.45852560G>TCA384491675ARID2c.4437G>T (p.Gln1479His)
c.646G>T
c.4358G>T
c.3990G>T (p.Gln1330His)
c.3267G>T (p.Gln1089His)
c.261G>T (p.Gln87His)
n.3728G>T
c.2805G>T (p.Gln935His)
n.4585G>T
n.4568G>T
dbSNP
12g.45852561G>ACA384491678ARID2c.4438G>A (p.Gly1480Arg)
c.647G>A
c.4359G>A
c.3991G>A (p.Gly1331Arg)
c.3268G>A (p.Gly1090Arg)
c.262G>A (p.Gly88Arg)
n.3729G>A
c.2806G>A (p.Gly936Arg)
n.4586G>A
n.4569G>A
dbSNP
12g.45852561G>CCA156966ARID2c.4438G>C (p.Gly1480Arg)
c.647G>C
c.4359G>C
c.3991G>C (p.Gly1331Arg)
c.3268G>C (p.Gly1090Arg)
c.262G>C (p.Gly88Arg)
n.3729G>C
c.2806G>C (p.Gly936Arg)
n.4586G>C
n.4569G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852561G=CA2033475669ARID2c.4438G= (p.Gly1480=)
c.647G=
c.4359G=
c.3991G= (p.Gly1331=)
c.3268G= (p.Gly1090=)
c.262G= (p.Gly88=)
n.3729G=
c.2806G= (p.Gly936=)
n.4586G=
n.4569G=
12g.45852561G>TCA384491680ARID2c.4438G>T (p.Gly1480Ter)
c.647G>T
c.4359G>T
c.3991G>T (p.Gly1331Ter)
c.3268G>T (p.Gly1090Ter)
c.262G>T (p.Gly88Ter)
n.3729G>T
c.2806G>T (p.Gly936Ter)
n.4586G>T
n.4569G>T
dbSNP
12g.45852562G>ACA384491684ARID2c.4439G>A (p.Gly1480Glu)
c.648G>A
c.4360G>A
c.3992G>A (p.Gly1331Glu)
c.3269G>A (p.Gly1090Glu)
c.263G>A (p.Gly88Glu)
n.3730G>A
c.2807G>A (p.Gly936Glu)
n.4587G>A
n.4570G>A
dbSNP gnomAD v4
12g.45852562G>CCA384491685ARID2c.4439G>C (p.Gly1480Ala)
c.648G>C
c.4360G>C
c.3992G>C (p.Gly1331Ala)
c.3269G>C (p.Gly1090Ala)
c.263G>C (p.Gly88Ala)
n.3730G>C
c.2807G>C (p.Gly936Ala)
n.4587G>C
n.4570G>C
dbSNP gnomAD v4
12g.45852562G>TCA384491688ARID2c.4439G>T (p.Gly1480Val)
c.648G>T
c.4360G>T
c.3992G>T (p.Gly1331Val)
c.3269G>T (p.Gly1090Val)
c.263G>T (p.Gly88Val)
n.3730G>T
c.2807G>T (p.Gly936Val)
n.4587G>T
n.4570G>T
dbSNP gnomAD v4
12g.45852563A=CA2033475671ARID2c.4440A= (p.Gly1480=)
c.649A=
c.4361A=
c.3993A= (p.Gly1331=)
c.3270A= (p.Gly1090=)
c.264A= (p.Gly88=)
n.3731A=
c.2808A= (p.Gly936=)
n.4588A=
n.4571A=
12g.45852563A>CCA479693822ARID2c.4440A>C (p.Gly1480=)
c.649A>C
c.4361A>C
c.3993A>C (p.Gly1331=)
c.3270A>C (p.Gly1090=)
c.264A>C (p.Gly88=)
n.3731A>C
c.2808A>C (p.Gly936=)
n.4588A>C
n.4571A>C
dbSNP
12g.45852563A>GCA479693824ARID2c.4440A>G (p.Gly1480=)
c.649A>G
c.4361A>G
c.3993A>G (p.Gly1331=)
c.3270A>G (p.Gly1090=)
c.264A>G (p.Gly88=)
n.3731A>G
c.2808A>G (p.Gly936=)
n.4588A>G
n.4571A>G
dbSNP gnomAD v3 gnomAD v4
12g.45852563A>TCA479693823ARID2c.4440A>T (p.Gly1480=)
c.649A>T
c.4361A>T
c.3993A>T (p.Gly1331=)
c.3270A>T (p.Gly1090=)
c.264A>T (p.Gly88=)
n.3731A>T
c.2808A>T (p.Gly936=)
n.4588A>T
n.4571A>T
dbSNP
12g.45852563_45852564delinsACCA2033475670ARID2c.4440_4441delinsAC (p.Gly1480=)
c.649_650delinsAC
c.4361_4362delinsAC
c.3993_3994delinsAC (p.Gly1331=)
c.3270_3271delinsAC (p.Gly1090=)
c.264_265delinsAC (p.Gly88=)
n.3731_3732delinsAC
c.2808_2809delinsAC (p.Gly936=)
n.4588_4589delinsAC
n.4571_4572delinsAC
12g.45852564delCA319652ARID2c.4441del (p.His1481IlefsTer4)
c.650del
c.4362del
c.3994del (p.His1332IlefsTer4)
c.3271del (p.His1091IlefsTer4)
c.265del (p.His89IlefsTer4)
n.3732del
c.2809del (p.His937IlefsTer4)
n.4589del
n.4572del
ClinVar dbSNP
12g.45852564C>ACA384491692ARID2c.4441C>A (p.His1481Asn)
c.650C>A
c.4362C>A
c.3994C>A (p.His1332Asn)
c.3271C>A (p.His1091Asn)
c.265C>A (p.His89Asn)
n.3732C>A
c.2809C>A (p.His937Asn)
n.4589C>A
n.4572C>A
12g.45852564C=CA2033475672ARID2c.4441C= (p.His1481=)
c.650C=
c.4362C=
c.3994C= (p.His1332=)
c.3271C= (p.His1091=)
c.265C= (p.His89=)
n.3732C=
c.2809C= (p.His937=)
n.4589C=
n.4572C=
12g.45852564C>GCA384491694ARID2c.4441C>G (p.His1481Asp)
c.650C>G
c.4362C>G
c.3994C>G (p.His1332Asp)
c.3271C>G (p.His1091Asp)
c.265C>G (p.His89Asp)
n.3732C>G
c.2809C>G (p.His937Asp)
n.4589C>G
n.4572C>G
dbSNP
12g.45852564C>TCA6526660ARID2c.4441C>T (p.His1481Tyr)
c.650C>T
c.4362C>T
c.3994C>T (p.His1332Tyr)
c.3271C>T (p.His1091Tyr)
c.265C>T (p.His89Tyr)
n.3732C>T
c.2809C>T (p.His937Tyr)
n.4589C>T
n.4572C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852565A=CA2033475673ARID2c.4442A= (p.His1481=)
c.651A=
c.4363A=
c.3995A= (p.His1332=)
c.3272A= (p.His1091=)
c.266A= (p.His89=)
n.3733A=
c.2810A= (p.His937=)
n.4590A=
n.4573A=
12g.45852565A>CCA6526661ARID2c.4442A>C (p.His1481Pro)
c.651A>C
c.4363A>C
c.3995A>C (p.His1332Pro)
c.3272A>C (p.His1091Pro)
c.266A>C (p.His89Pro)
n.3733A>C
c.2810A>C (p.His937Pro)
n.4590A>C
n.4573A>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852565A>GCA236400732ARID2c.4442A>G (p.His1481Arg)
c.651A>G
c.4363A>G
c.3995A>G (p.His1332Arg)
c.3272A>G (p.His1091Arg)
c.266A>G (p.His89Arg)
n.3733A>G
c.2810A>G (p.His937Arg)
n.4590A>G
n.4573A>G
dbSNP gnomAD v4
12g.45852565A>TCA384491703ARID2c.4442A>T (p.His1481Leu)
c.651A>T
c.4363A>T
c.3995A>T (p.His1332Leu)
c.3272A>T (p.His1091Leu)
c.266A>T (p.His89Leu)
n.3733A>T
c.2810A>T (p.His937Leu)
n.4590A>T
n.4573A>T
dbSNP
12g.45852566T>ACA384491708ARID2c.4443T>A (p.His1481Gln)
c.652T>A
c.4364T>A
c.3996T>A (p.His1332Gln)
c.3273T>A (p.His1091Gln)
c.267T>A (p.His89Gln)
n.3734T>A
c.2811T>A (p.His937Gln)
n.4591T>A
n.4574T>A
dbSNP
12g.45852566T>CCA479693825ARID2c.4443T>C (p.His1481=)
c.652T>C
c.4364T>C
c.3996T>C (p.His1332=)
c.3273T>C (p.His1091=)
c.267T>C (p.His89=)
n.3734T>C
c.2811T>C (p.His937=)
n.4591T>C
n.4574T>C
dbSNP
12g.45852566T>GCA384491710ARID2c.4443T>G (p.His1481Gln)
c.652T>G
c.4364T>G
c.3996T>G (p.His1332Gln)
c.3273T>G (p.His1091Gln)
c.267T>G (p.His89Gln)
n.3734T>G
c.2811T>G (p.His937Gln)
n.4591T>G
n.4574T>G
dbSNP gnomAD v2 gnomAD v4
12g.45852566T=CA2033475674ARID2c.4443T= (p.His1481=)
c.652T=
c.4364T=
c.3996T= (p.His1332=)
c.3273T= (p.His1091=)
c.267T= (p.His89=)
n.3734T=
c.2811T= (p.His937=)
n.4591T=
n.4574T=
12g.45852567C>ACA384491716ARID2c.4444C>A (p.Gln1482Lys)
c.653C>A
c.4365C>A
c.3997C>A (p.Gln1333Lys)
c.3274C>A (p.Gln1092Lys)
c.268C>A (p.Gln90Lys)
n.3735C>A
c.2812C>A (p.Gln938Lys)
n.4592C>A
n.4575C>A
dbSNP
12g.45852567C=CA2033475675ARID2c.4444C= (p.Gln1482=)
c.653C=
c.4365C=
c.3997C= (p.Gln1333=)
c.3274C= (p.Gln1092=)
c.268C= (p.Gln90=)
n.3735C=
c.2812C= (p.Gln938=)
n.4592C=
n.4575C=
12g.45852567C>GCA384491714ARID2c.4444C>G (p.Gln1482Glu)
c.653C>G
c.4365C>G
c.3997C>G (p.Gln1333Glu)
c.3274C>G (p.Gln1092Glu)
c.268C>G (p.Gln90Glu)
n.3735C>G
c.2812C>G (p.Gln938Glu)
n.4592C>G
n.4575C>G
dbSNP
12g.45852567C>TCA384491712ARID2c.4444C>T (p.Gln1482Ter)
c.653C>T
c.4365C>T
c.3997C>T (p.Gln1333Ter)
c.3274C>T (p.Gln1092Ter)
c.268C>T (p.Gln90Ter)
n.3735C>T
c.2812C>T (p.Gln938Ter)
n.4592C>T
n.4575C>T
dbSNP gnomAD v2 COSMIC
12g.45852568A=CA2033475676ARID2c.4445A= (p.Gln1482=)
c.654A=
c.4366A=
c.3998A= (p.Gln1333=)
c.3275A= (p.Gln1092=)
c.269A= (p.Gln90=)
n.3736A=
c.2813A= (p.Gln938=)
n.4593A=
n.4576A=
12g.45852568A>CCA384491720ARID2c.4445A>C (p.Gln1482Pro)
c.654A>C
c.4366A>C
c.3998A>C (p.Gln1333Pro)
c.3275A>C (p.Gln1092Pro)
c.269A>C (p.Gln90Pro)
n.3736A>C
c.2813A>C (p.Gln938Pro)
n.4593A>C
n.4576A>C
12g.45852568A>GCA384491722ARID2c.4445A>G (p.Gln1482Arg)
c.654A>G
c.4366A>G
c.3998A>G (p.Gln1333Arg)
c.3275A>G (p.Gln1092Arg)
c.269A>G (p.Gln90Arg)
n.3736A>G
c.2813A>G (p.Gln938Arg)
n.4593A>G
n.4576A>G
dbSNP
12g.45852568A>TCA384491724ARID2c.4445A>T (p.Gln1482Leu)
c.654A>T
c.4366A>T
c.3998A>T (p.Gln1333Leu)
c.3275A>T (p.Gln1092Leu)
c.269A>T (p.Gln90Leu)
n.3736A>T
c.2813A>T (p.Gln938Leu)
n.4593A>T
n.4576A>T
dbSNP
12g.45852568_45852569insGCA604811920ARID2c.4445_4446insG (p.Ile1483AsnfsTer20)
c.654_655insG
c.4366_4367insG
c.3998_3999insG (p.Ile1334AsnfsTer20)
c.3275_3276insG (p.Ile1093AsnfsTer20)
c.269_270insG (p.Ile91AsnfsTer20)
n.3736_3737insG
c.2813_2814insG (p.Ile939AsnfsTer20)
n.4593_4594insG
n.4576_4577insG
dbSNP gnomAD v2
12g.45852569A=CA2033475677ARID2c.4446A= (p.Gln1482=)
c.655A=
c.4367A=
c.3999A= (p.Gln1333=)
c.3276A= (p.Gln1092=)
c.270A= (p.Gln90=)
n.3737A=
c.2814A= (p.Gln938=)
n.4594A=
n.4577A=
12g.45852569A>CCA384491726ARID2c.4446A>C (p.Gln1482His)
c.655A>C
c.4367A>C
c.3999A>C (p.Gln1333His)
c.3276A>C (p.Gln1092His)
c.270A>C (p.Gln90His)
n.3737A>C
c.2814A>C (p.Gln938His)
n.4594A>C
n.4577A>C
COSMIC
12g.45852569A>GCA479693826ARID2c.4446A>G (p.Gln1482=)
c.655A>G
c.4367A>G
c.3999A>G (p.Gln1333=)
c.3276A>G (p.Gln1092=)
c.270A>G (p.Gln90=)
n.3737A>G
c.2814A>G (p.Gln938=)
n.4594A>G
n.4577A>G
dbSNP gnomAD v4
12g.45852569A>TCA384491728ARID2c.4446A>T (p.Gln1482His)
c.655A>T
c.4367A>T
c.3999A>T (p.Gln1333His)
c.3276A>T (p.Gln1092His)
c.270A>T (p.Gln90His)
n.3737A>T
c.2814A>T (p.Gln938His)
n.4594A>T
n.4577A>T
dbSNP
12g.45852570A=CA2033475678ARID2c.4447A= (p.Ile1483=)
c.656A=
c.4368A=
c.4000A= (p.Ile1334=)
c.3277A= (p.Ile1093=)
c.271A= (p.Ile91=)
n.3738A=
c.2815A= (p.Ile939=)
n.4595A=
n.4578A=
12g.45852570A>CCA384491733ARID2c.4447A>C (p.Ile1483Leu)
c.656A>C
c.4368A>C
c.4000A>C (p.Ile1334Leu)
c.3277A>C (p.Ile1093Leu)
c.271A>C (p.Ile91Leu)
n.3738A>C
c.2815A>C (p.Ile939Leu)
n.4595A>C
n.4578A>C
12g.45852570A>GCA384491734ARID2c.4447A>G (p.Ile1483Val)
c.656A>G
c.4368A>G
c.4000A>G (p.Ile1334Val)
c.3277A>G (p.Ile1093Val)
c.271A>G (p.Ile91Val)
n.3738A>G
c.2815A>G (p.Ile939Val)
n.4595A>G
n.4578A>G
dbSNP gnomAD v2 gnomAD v4
12g.45852570A>TCA384491736ARID2c.4447A>T (p.Ile1483Phe)
c.656A>T
c.4368A>T
c.4000A>T (p.Ile1334Phe)
c.3277A>T (p.Ile1093Phe)
c.271A>T (p.Ile91Phe)
n.3738A>T
c.2815A>T (p.Ile939Phe)
n.4595A>T
n.4578A>T
dbSNP
12g.45852570_45852571insATTCTTTCTAGTTGACA604811921ARID2c.4447_4448insATTCTTTCTAGTTGA (p.Ile1483AsnfsTer4)
c.656_657insATTCTTTCTAGTTGA
c.4368_4369insATTCTTTCTAGTTGA
c.4000_4001insATTCTTTCTAGTTGA (p.Ile1334AsnfsTer4)
c.3277_3278insATTCTTTCTAGTTGA (p.Ile1093AsnfsTer4)
c.271_272insATTCTTTCTAGTTGA (p.Ile91AsnfsTer4)
n.3738_3739insATTCTTTCTAGTTGA
c.2815_2816insATTCTTTCTAGTTGA (p.Ile939AsnfsTer4)
n.4595_4596insATTCTTTCTAGTTGA
n.4578_4579insATTCTTTCTAGTTGA
dbSNP gnomAD v2
12g.45852570_45852571insATTCTTCA2033475679ARID2c.4447_4448insATTCTT (p.Ile1483delinsAsnSerPhe)
c.656_657insATTCTT
c.4368_4369insATTCTT
c.4000_4001insATTCTT (p.Ile1334delinsAsnSerPhe)
c.3277_3278insATTCTT (p.Ile1093delinsAsnSerPhe)
c.271_272insATTCTT (p.Ile91delinsAsnSerPhe)
n.3738_3739insATTCTT
c.2815_2816insATTCTT (p.Ile939delinsAsnSerPhe)
n.4595_4596insATTCTT
n.4578_4579insATTCTT
dbSNP
12g.45852571T>ACA384491739ARID2c.4448T>A (p.Ile1483Asn)
c.657T>A
c.4369T>A
c.4001T>A (p.Ile1334Asn)
c.3278T>A (p.Ile1093Asn)
c.272T>A (p.Ile91Asn)
n.3739T>A
c.2816T>A (p.Ile939Asn)
n.4596T>A
n.4579T>A
dbSNP
12g.45852571T>CCA6526662ARID2c.4448T>C (p.Ile1483Thr)
c.657T>C
c.4369T>C
c.4001T>C (p.Ile1334Thr)
c.3278T>C (p.Ile1093Thr)
c.272T>C (p.Ile91Thr)
n.3739T>C
c.2816T>C (p.Ile939Thr)
n.4596T>C
n.4579T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852571T>GCA384491742ARID2c.4448T>G (p.Ile1483Ser)
c.657T>G
c.4369T>G
c.4001T>G (p.Ile1334Ser)
c.3278T>G (p.Ile1093Ser)
c.272T>G (p.Ile91Ser)
n.3739T>G
c.2816T>G (p.Ile939Ser)
n.4596T>G
n.4579T>G
dbSNP
12g.45852571T=CA2033475680ARID2c.4448T= (p.Ile1483=)
c.657T=
c.4369T=
c.4001T= (p.Ile1334=)
c.3278T= (p.Ile1093=)
c.272T= (p.Ile91=)
n.3739T=
c.2816T= (p.Ile939=)
n.4596T=
n.4579T=
12g.45852572C>ACA479693827ARID2c.4449C>A (p.Ile1483=)
c.658C>A
c.4370C>A
c.4002C>A (p.Ile1334=)
c.3279C>A (p.Ile1093=)
c.273C>A (p.Ile91=)
n.3740C>A
c.2817C>A (p.Ile939=)
n.4597C>A
n.4580C>A
dbSNP
12g.45852572C>GCA384491745ARID2c.4449C>G (p.Ile1483Met)
c.658C>G
c.4370C>G
c.4002C>G (p.Ile1334Met)
c.3279C>G (p.Ile1093Met)
c.273C>G (p.Ile91Met)
n.3740C>G
c.2817C>G (p.Ile939Met)
n.4597C>G
n.4580C>G
dbSNP
12g.45852572C>TCA479693828ARID2c.4449C>T (p.Ile1483=)
c.658C>T
c.4370C>T
c.4002C>T (p.Ile1334=)
c.3279C>T (p.Ile1093=)
c.273C>T (p.Ile91=)
n.3740C>T
c.2817C>T (p.Ile939=)
n.4597C>T
n.4580C>T
dbSNP
12g.45852573A=CA2033475681ARID2c.4450A= (p.Ile1484=)
c.659A=
c.4371A=
c.4003A= (p.Ile1335=)
c.3280A= (p.Ile1094=)
c.274A= (p.Ile92=)
n.3741A=
c.2818A= (p.Ile940=)
n.4598A=
n.4581A=
12g.45852573A>CCA384491748ARID2c.4450A>C (p.Ile1484Leu)
c.659A>C
c.4371A>C
c.4003A>C (p.Ile1335Leu)
c.3280A>C (p.Ile1094Leu)
c.274A>C (p.Ile92Leu)
n.3741A>C
c.2818A>C (p.Ile940Leu)
n.4598A>C
n.4581A>C
dbSNP
12g.45852573A>GCA6526664ARID2c.4450A>G (p.Ile1484Val)
c.659A>G
c.4371A>G
c.4003A>G (p.Ile1335Val)
c.3280A>G (p.Ile1094Val)
c.274A>G (p.Ile92Val)
n.3741A>G
c.2818A>G (p.Ile940Val)
n.4598A>G
n.4581A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852573A>TCA6526663ARID2c.4450A>T (p.Ile1484Leu)
c.659A>T
c.4371A>T
c.4003A>T (p.Ile1335Leu)
c.3280A>T (p.Ile1094Leu)
c.274A>T (p.Ile92Leu)
n.3741A>T
c.2818A>T (p.Ile940Leu)
n.4598A>T
n.4581A>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852574T>ACA236400748ARID2c.4451T>A (p.Ile1484Lys)
c.660T>A
c.4372T>A
c.4004T>A (p.Ile1335Lys)
c.3281T>A (p.Ile1094Lys)
c.275T>A (p.Ile92Lys)
n.3742T>A
c.2819T>A (p.Ile940Lys)
n.4599T>A
n.4582T>A
dbSNP
12g.45852574T>CCA6526665ARID2c.4451T>C (p.Ile1484Thr)
c.660T>C
c.4372T>C
c.4004T>C (p.Ile1335Thr)
c.3281T>C (p.Ile1094Thr)
c.275T>C (p.Ile92Thr)
n.3742T>C
c.2819T>C (p.Ile940Thr)
n.4599T>C
n.4582T>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852574T>GCA384491755ARID2c.4451T>G (p.Ile1484Arg)
c.660T>G
c.4372T>G
c.4004T>G (p.Ile1335Arg)
c.3281T>G (p.Ile1094Arg)
c.275T>G (p.Ile92Arg)
n.3742T>G
c.2819T>G (p.Ile940Arg)
n.4599T>G
n.4582T>G
12g.45852574T=CA2033475682ARID2c.4451T= (p.Ile1484=)
c.660T=
c.4372T=
c.4004T= (p.Ile1335=)
c.3281T= (p.Ile1094=)
c.275T= (p.Ile92=)
n.3742T=
c.2819T= (p.Ile940=)
n.4599T=
n.4582T=
12g.45852575A>CCA479693829ARID2c.4452A>C (p.Ile1484=)
c.661A>C
c.4373A>C
c.4005A>C (p.Ile1335=)
c.3282A>C (p.Ile1094=)
c.276A>C (p.Ile92=)
n.3743A>C
c.2820A>C (p.Ile940=)
n.4600A>C
n.4583A>C
12g.45852575A>GCA384491759ARID2c.4452A>G (p.Ile1484Met)
c.661A>G
c.4373A>G
c.4005A>G (p.Ile1335Met)
c.3282A>G (p.Ile1094Met)
c.276A>G (p.Ile92Met)
n.3743A>G
c.2820A>G (p.Ile940Met)
n.4600A>G
n.4583A>G
dbSNP gnomAD v4
12g.45852575A>TCA479693830ARID2c.4452A>T (p.Ile1484=)
c.661A>T
c.4373A>T
c.4005A>T (p.Ile1335=)
c.3282A>T (p.Ile1094=)
c.276A>T (p.Ile92=)
n.3743A>T
c.2820A>T (p.Ile940=)
n.4600A>T
n.4583A>T
dbSNP gnomAD v4
12g.45852576G>ACA384491762ARID2c.4453G>A (p.Ala1485Thr)
c.662G>A
c.4374G>A
c.4006G>A (p.Ala1336Thr)
c.3283G>A (p.Ala1095Thr)
c.277G>A (p.Ala93Thr)
n.3744G>A
c.2821G>A (p.Ala941Thr)
n.4601G>A
n.4584G>A
dbSNP
12g.45852576G>CCA384491764ARID2c.4453G>C (p.Ala1485Pro)
c.662G>C
c.4374G>C
c.4006G>C (p.Ala1336Pro)
c.3283G>C (p.Ala1095Pro)
c.277G>C (p.Ala93Pro)
n.3744G>C
c.2821G>C (p.Ala941Pro)
n.4601G>C
n.4584G>C
dbSNP
12g.45852576G>TCA384491765ARID2c.4453G>T (p.Ala1485Ser)
c.662G>T
c.4374G>T
c.4006G>T (p.Ala1336Ser)
c.3283G>T (p.Ala1095Ser)
c.277G>T (p.Ala93Ser)
n.3744G>T
c.2821G>T (p.Ala941Ser)
n.4601G>T
n.4584G>T
dbSNP
12g.45852577C>ACA384491766ARID2c.4454C>A (p.Ala1485Glu)
c.663C>A
c.4375C>A
c.4007C>A (p.Ala1336Glu)
c.3284C>A (p.Ala1095Glu)
c.278C>A (p.Ala93Glu)
n.3745C>A
c.2822C>A (p.Ala941Glu)
n.4602C>A
n.4585C>A
12g.45852577C=CA2033475683ARID2c.4454C= (p.Ala1485=)
c.663C=
c.4375C=
c.4007C= (p.Ala1336=)
c.3284C= (p.Ala1095=)
c.278C= (p.Ala93=)
n.3745C=
c.2822C= (p.Ala941=)
n.4602C=
n.4585C=
12g.45852577C>GCA384491767ARID2c.4454C>G (p.Ala1485Gly)
c.663C>G
c.4375C>G
c.4007C>G (p.Ala1336Gly)
c.3284C>G (p.Ala1095Gly)
c.278C>G (p.Ala93Gly)
n.3745C>G
c.2822C>G (p.Ala941Gly)
n.4602C>G
n.4585C>G
12g.45852577C>TCA384491768ARID2c.4454C>T (p.Ala1485Val)
c.663C>T
c.4375C>T
c.4007C>T (p.Ala1336Val)
c.3284C>T (p.Ala1095Val)
c.278C>T (p.Ala93Val)
n.3745C>T
c.2822C>T (p.Ala941Val)
n.4602C>T
n.4585C>T
dbSNP gnomAD v2
12g.45852578A>CCA479693831ARID2c.4455A>C (p.Ala1485=)
c.664A>C
c.4376A>C
c.4008A>C (p.Ala1336=)
c.3285A>C (p.Ala1095=)
c.279A>C (p.Ala93=)
n.3746A>C
c.2823A>C (p.Ala941=)
n.4603A>C
n.4586A>C
12g.45852578A>GCA479693832ARID2c.4455A>G (p.Ala1485=)
c.664A>G
c.4376A>G
c.4008A>G (p.Ala1336=)
c.3285A>G (p.Ala1095=)
c.279A>G (p.Ala93=)
n.3746A>G
c.2823A>G (p.Ala941=)
n.4603A>G
n.4586A>G
dbSNP
12g.45852578A>TCA479693833ARID2c.4455A>T (p.Ala1485=)
c.664A>T
c.4376A>T
c.4008A>T (p.Ala1336=)
c.3285A>T (p.Ala1095=)
c.279A>T (p.Ala93=)
n.3746A>T
c.2823A>T (p.Ala941=)
n.4603A>T
n.4586A>T
dbSNP
12g.45852579G>ACA384491769ARID2c.4456G>A (p.Val1486Ile)
c.665G>A
c.4377G>A
c.4009G>A (p.Val1337Ile)
c.3286G>A (p.Val1096Ile)
c.280G>A (p.Val94Ile)
n.3747G>A
c.2824G>A (p.Val942Ile)
n.4604G>A
n.4587G>A
dbSNP
12g.45852579G>CCA384491770ARID2c.4456G>C (p.Val1486Leu)
c.665G>C
c.4377G>C
c.4009G>C (p.Val1337Leu)
c.3286G>C (p.Val1096Leu)
c.280G>C (p.Val94Leu)
n.3747G>C
c.2824G>C (p.Val942Leu)
n.4604G>C
n.4587G>C
dbSNP
12g.45852579G>TCA384491771ARID2c.4456G>T (p.Val1486Phe)
c.665G>T
c.4377G>T
c.4009G>T (p.Val1337Phe)
c.3286G>T (p.Val1096Phe)
c.280G>T (p.Val94Phe)
n.3747G>T
c.2824G>T (p.Val942Phe)
n.4604G>T
n.4587G>T
12g.45852580T>ACA384491772ARID2c.4457T>A (p.Val1486Asp)
c.666T>A
c.4378T>A
c.4010T>A (p.Val1337Asp)
c.3287T>A (p.Val1096Asp)
c.281T>A (p.Val94Asp)
n.3748T>A
c.2825T>A (p.Val942Asp)
n.4605T>A
n.4588T>A
dbSNP
12g.45852580T>CCA384491773ARID2c.4457T>C (p.Val1486Ala)
c.666T>C
c.4378T>C
c.4010T>C (p.Val1337Ala)
c.3287T>C (p.Val1096Ala)
c.281T>C (p.Val94Ala)
n.3748T>C
c.2825T>C (p.Val942Ala)
n.4605T>C
n.4588T>C
dbSNP
12g.45852580T>GCA384491774ARID2c.4457T>G (p.Val1486Gly)
c.666T>G
c.4378T>G
c.4010T>G (p.Val1337Gly)
c.3287T>G (p.Val1096Gly)
c.281T>G (p.Val94Gly)
n.3748T>G
c.2825T>G (p.Val942Gly)
n.4605T>G
n.4588T>G
dbSNP
12g.45852581T>ACA479693835ARID2c.4458T>A (p.Val1486=)
c.667T>A
c.4379T>A
c.4011T>A (p.Val1337=)
c.3288T>A (p.Val1096=)
c.282T>A (p.Val94=)
n.3749T>A
c.2826T>A (p.Val942=)
n.4606T>A
n.4589T>A
12g.45852581T>CCA479693836ARID2c.4458T>C (p.Val1486=)
c.667T>C
c.4379T>C
c.4011T>C (p.Val1337=)
c.3288T>C (p.Val1096=)
c.282T>C (p.Val94=)
n.3749T>C
c.2826T>C (p.Val942=)
n.4606T>C
n.4589T>C
12g.45852581T>GCA479693834ARID2c.4458T>G (p.Val1486=)
c.667T>G
c.4379T>G
c.4011T>G (p.Val1337=)
c.3288T>G (p.Val1096=)
c.282T>G (p.Val94=)
n.3749T>G
c.2826T>G (p.Val942=)
n.4606T>G
n.4589T>G
12g.45852582C>ACA384491777ARID2c.4459C>A (p.Pro1487Thr)
c.668C>A
c.4380C>A
c.4012C>A (p.Pro1338Thr)
c.3289C>A (p.Pro1097Thr)
c.283C>A (p.Pro95Thr)
n.3750C>A
c.2827C>A (p.Pro943Thr)
n.4607C>A
n.4590C>A
dbSNP COSMIC
12g.45852582C>GCA384491775ARID2c.4459C>G (p.Pro1487Ala)
c.668C>G
c.4380C>G
c.4012C>G (p.Pro1338Ala)
c.3289C>G (p.Pro1097Ala)
c.283C>G (p.Pro95Ala)
n.3750C>G
c.2827C>G (p.Pro943Ala)
n.4607C>G
n.4590C>G
dbSNP
12g.45852582C>TCA384491776ARID2c.4459C>T (p.Pro1487Ser)
c.668C>T
c.4380C>T
c.4012C>T (p.Pro1338Ser)
c.3289C>T (p.Pro1097Ser)
c.283C>T (p.Pro95Ser)
n.3750C>T
c.2827C>T (p.Pro943Ser)
n.4607C>T
n.4590C>T
dbSNP gnomAD v4
12g.45852583C>ACA384491778ARID2c.4460C>A (p.Pro1487His)
c.669C>A
c.4381C>A
c.4013C>A (p.Pro1338His)
c.3290C>A (p.Pro1097His)
c.284C>A (p.Pro95His)
n.3751C>A
c.2828C>A (p.Pro943His)
n.4608C>A
n.4591C>A
dbSNP
12g.45852583C>GCA384491779ARID2c.4460C>G (p.Pro1487Arg)
c.669C>G
c.4381C>G
c.4013C>G (p.Pro1338Arg)
c.3290C>G (p.Pro1097Arg)
c.284C>G (p.Pro95Arg)
n.3751C>G
c.2828C>G (p.Pro943Arg)
n.4608C>G
n.4591C>G
dbSNP
12g.45852583C>TCA384491780ARID2c.4460C>T (p.Pro1487Leu)
c.669C>T
c.4381C>T
c.4013C>T (p.Pro1338Leu)
c.3290C>T (p.Pro1097Leu)
c.284C>T (p.Pro95Leu)
n.3751C>T
c.2828C>T (p.Pro943Leu)
n.4608C>T
n.4591C>T
dbSNP COSMIC
12g.45852584C>ACA479693837ARID2c.4461C>A (p.Pro1487=)
c.670C>A
c.4382C>A
c.4014C>A (p.Pro1338=)
c.3291C>A (p.Pro1097=)
c.285C>A (p.Pro95=)
n.3752C>A
c.2829C>A (p.Pro943=)
n.4609C>A
n.4592C>A
dbSNP
12g.45852584C=CA2033475684ARID2c.4461C= (p.Pro1487=)
c.670C=
c.4382C=
c.4014C= (p.Pro1338=)
c.3291C= (p.Pro1097=)
c.285C= (p.Pro95=)
n.3752C=
c.2829C= (p.Pro943=)
n.4609C=
n.4592C=
12g.45852584C>GCA236400753ARID2c.4461C>G (p.Pro1487=)
c.670C>G
c.4382C>G
c.4014C>G (p.Pro1338=)
c.3291C>G (p.Pro1097=)
c.285C>G (p.Pro95=)
n.3752C>G
c.2829C>G (p.Pro943=)
n.4609C>G
n.4592C>G
dbSNP gnomAD v4
12g.45852584C>TCA6526666ARID2c.4461C>T (p.Pro1487=)
c.670C>T
c.4382C>T
c.4014C>T (p.Pro1338=)
c.3291C>T (p.Pro1097=)
c.285C>T (p.Pro95=)
n.3752C>T
c.2829C>T (p.Pro943=)
n.4609C>T
n.4592C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852585G>ACA6526667ARID2c.4462G>A (p.Asp1488Asn)
c.671G>A
c.4383G>A
c.4015G>A (p.Asp1339Asn)
c.3292G>A (p.Asp1098Asn)
c.286G>A (p.Asp96Asn)
n.3753G>A
c.2830G>A (p.Asp944Asn)
n.4610G>A
n.4593G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852585G>CCA384491781ARID2c.4462G>C (p.Asp1488His)
c.671G>C
c.4383G>C
c.4015G>C (p.Asp1339His)
c.3292G>C (p.Asp1098His)
c.286G>C (p.Asp96His)
n.3753G>C
c.2830G>C (p.Asp944His)
n.4610G>C
n.4593G>C
dbSNP
12g.45852585G=CA2033475685ARID2c.4462G= (p.Asp1488=)
c.671G=
c.4383G=
c.4015G= (p.Asp1339=)
c.3292G= (p.Asp1098=)
c.286G= (p.Asp96=)
n.3753G=
c.2830G= (p.Asp944=)
n.4610G=
n.4593G=
12g.45852585G>TCA384491782ARID2c.4462G>T (p.Asp1488Tyr)
c.671G>T
c.4383G>T
c.4015G>T (p.Asp1339Tyr)
c.3292G>T (p.Asp1098Tyr)
c.286G>T (p.Asp96Tyr)
n.3753G>T
c.2830G>T (p.Asp944Tyr)
n.4610G>T
n.4593G>T
dbSNP
12g.45852586A>CCA384491783ARID2c.4463A>C (p.Asp1488Ala)
c.672A>C
c.4384A>C
c.4016A>C (p.Asp1339Ala)
c.3293A>C (p.Asp1098Ala)
c.287A>C (p.Asp96Ala)
n.3754A>C
c.2831A>C (p.Asp944Ala)
n.4611A>C
n.4594A>C
dbSNP
12g.45852586A>GCA384491784ARID2c.4463A>G (p.Asp1488Gly)
c.672A>G
c.4384A>G
c.4016A>G (p.Asp1339Gly)
c.3293A>G (p.Asp1098Gly)
c.287A>G (p.Asp96Gly)
n.3754A>G
c.2831A>G (p.Asp944Gly)
n.4611A>G
n.4594A>G
dbSNP
12g.45852586A>TCA384491785ARID2c.4463A>T (p.Asp1488Val)
c.672A>T
c.4384A>T
c.4016A>T (p.Asp1339Val)
c.3293A>T (p.Asp1098Val)
c.287A>T (p.Asp96Val)
n.3754A>T
c.2831A>T (p.Asp944Val)
n.4611A>T
n.4594A>T
dbSNP
12g.45852587_45852599delCA645571099ARID2c.4464_4476del (p.Asp1488GlufsTer24)
c.673_685del
c.4385_4397del
c.4017_4029del (p.Asp1339GlufsTer24)
c.3294_3306del (p.Asp1098GlufsTer24)
c.288_300del (p.Asp96GlufsTer24)
n.3755_3767del
c.2832_2844del (p.Asp944GlufsTer24)
n.4612_4624del
n.4595_4607del
COSMIC
12g.45852587C>ACA384491786ARID2c.4464C>A (p.Asp1488Glu)
c.673C>A
c.4385C>A
c.4017C>A (p.Asp1339Glu)
c.3294C>A (p.Asp1098Glu)
c.288C>A (p.Asp96Glu)
n.3755C>A
c.2832C>A (p.Asp944Glu)
n.4612C>A
n.4595C>A
12g.45852587C=CA2033475686ARID2c.4464C= (p.Asp1488=)
c.673C=
c.4385C=
c.4017C= (p.Asp1339=)
c.3294C= (p.Asp1098=)
c.288C= (p.Asp96=)
n.3755C=
c.2832C= (p.Asp944=)
n.4612C=
n.4595C=
12g.45852587C>GCA384491787ARID2c.4464C>G (p.Asp1488Glu)
c.673C>G
c.4385C>G
c.4017C>G (p.Asp1339Glu)
c.3294C>G (p.Asp1098Glu)
c.288C>G (p.Asp96Glu)
n.3755C>G
c.2832C>G (p.Asp944Glu)
n.4612C>G
n.4595C>G
12g.45852587C>TCA479693838ARID2c.4464C>T (p.Asp1488=)
c.673C>T
c.4385C>T
c.4017C>T (p.Asp1339=)
c.3294C>T (p.Asp1098=)
c.288C>T (p.Asp96=)
n.3755C>T
c.2832C>T (p.Asp944=)
n.4612C>T
n.4595C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.45852588T>ACA384491788ARID2c.4465T>A (p.Ser1489Thr)
c.674T>A
c.4386T>A
c.4018T>A (p.Ser1340Thr)
c.3295T>A (p.Ser1099Thr)
c.289T>A (p.Ser97Thr)
n.3756T>A
c.2833T>A (p.Ser945Thr)
n.4613T>A
n.4596T>A
12g.45852588T>CCA384491790ARID2c.4465T>C (p.Ser1489Pro)
c.674T>C
c.4386T>C
c.4018T>C (p.Ser1340Pro)
c.3295T>C (p.Ser1099Pro)
c.289T>C (p.Ser97Pro)
n.3756T>C
c.2833T>C (p.Ser945Pro)
n.4613T>C
n.4596T>C
12g.45852588T>GCA384491789ARID2c.4465T>G (p.Ser1489Ala)
c.674T>G
c.4386T>G
c.4018T>G (p.Ser1340Ala)
c.3295T>G (p.Ser1099Ala)
c.289T>G (p.Ser97Ala)
n.3756T>G
c.2833T>G (p.Ser945Ala)
n.4613T>G
n.4596T>G
dbSNP
12g.45852589C>ACA384491791ARID2c.4466C>A (p.Ser1489Ter)
c.675C>A
c.4387C>A
c.4019C>A (p.Ser1340Ter)
c.3296C>A (p.Ser1099Ter)
c.290C>A (p.Ser97Ter)
n.3757C>A
c.2834C>A (p.Ser945Ter)
n.4614C>A
n.4597C>A
12g.45852589C=CA2033475687ARID2c.4466C= (p.Ser1489=)
c.675C=
c.4387C=
c.4019C= (p.Ser1340=)
c.3296C= (p.Ser1099=)
c.290C= (p.Ser97=)
n.3757C=
c.2834C= (p.Ser945=)
n.4614C=
n.4597C=
12g.45852589C>GCA384491792ARID2c.4466C>G (p.Ser1489Ter)
c.675C>G
c.4387C>G
c.4019C>G (p.Ser1340Ter)
c.3296C>G (p.Ser1099Ter)
c.290C>G (p.Ser97Ter)
n.3757C>G
c.2834C>G (p.Ser945Ter)
n.4614C>G
n.4597C>G
dbSNP COSMIC
12g.45852589C>TCA384491793ARID2c.4466C>T (p.Ser1489Leu)
c.675C>T
c.4387C>T
c.4019C>T (p.Ser1340Leu)
c.3296C>T (p.Ser1099Leu)
c.290C>T (p.Ser97Leu)
n.3757C>T
c.2834C>T (p.Ser945Leu)
n.4614C>T
n.4597C>T
dbSNP
12g.45852590A>CCA479693839ARID2c.4467A>C (p.Ser1489=)
c.676A>C
c.4388A>C
c.4020A>C (p.Ser1340=)
c.3297A>C (p.Ser1099=)
c.291A>C (p.Ser97=)
n.3758A>C
c.2835A>C (p.Ser945=)
n.4615A>C
n.4598A>C
dbSNP
12g.45852590A>GCA479693840ARID2c.4467A>G (p.Ser1489=)
c.676A>G
c.4388A>G
c.4020A>G (p.Ser1340=)
c.3297A>G (p.Ser1099=)
c.291A>G (p.Ser97=)
n.3758A>G
c.2835A>G (p.Ser945=)
n.4615A>G
n.4598A>G
dbSNP gnomAD v4
12g.45852590A>TCA479693841ARID2c.4467A>T (p.Ser1489=)
c.676A>T
c.4388A>T
c.4020A>T (p.Ser1340=)
c.3297A>T (p.Ser1099=)
c.291A>T (p.Ser97=)
n.3758A>T
c.2835A>T (p.Ser945=)
n.4615A>T
n.4598A>T
dbSNP
12g.45852591G>ACA384491794ARID2c.4468G>A (p.Gly1490Arg)
c.677G>A
c.4389G>A
c.4021G>A (p.Gly1341Arg)
c.3298G>A (p.Gly1100Arg)
c.292G>A (p.Gly98Arg)
n.3759G>A
c.2836G>A (p.Gly946Arg)
n.4616G>A
n.4599G>A
dbSNP
12g.45852591G>CCA384491795ARID2c.4468G>C (p.Gly1490Arg)
c.677G>C
c.4389G>C
c.4021G>C (p.Gly1341Arg)
c.3298G>C (p.Gly1100Arg)
c.292G>C (p.Gly98Arg)
n.3759G>C
c.2836G>C (p.Gly946Arg)
n.4616G>C
n.4599G>C
dbSNP
12g.45852591G=CA2033475688ARID2c.4468G= (p.Gly1490=)
c.677G=
c.4389G=
c.4021G= (p.Gly1341=)
c.3298G= (p.Gly1100=)
c.292G= (p.Gly98=)
n.3759G=
c.2836G= (p.Gly946=)
n.4616G=
n.4599G=
12g.45852591G>TCA384491796ARID2c.4468G>T (p.Gly1490Ter)
c.677G>T
c.4389G>T
c.4021G>T (p.Gly1341Ter)
c.3298G>T (p.Gly1100Ter)
c.292G>T (p.Gly98Ter)
n.3759G>T
c.2836G>T (p.Gly946Ter)
n.4616G>T
n.4599G>T
dbSNP gnomAD v2
12g.45852592G>ACA384491797ARID2c.4469G>A (p.Gly1490Glu)
c.678G>A
c.4390G>A
c.4022G>A (p.Gly1341Glu)
c.3299G>A (p.Gly1100Glu)
c.293G>A (p.Gly98Glu)
n.3760G>A
c.2837G>A (p.Gly946Glu)
n.4617G>A
n.4600G>A
dbSNP gnomAD v2 gnomAD v4
12g.45852592G>CCA384491798ARID2c.4469G>C (p.Gly1490Ala)
c.678G>C
c.4390G>C
c.4022G>C (p.Gly1341Ala)
c.3299G>C (p.Gly1100Ala)
c.293G>C (p.Gly98Ala)
n.3760G>C
c.2837G>C (p.Gly946Ala)
n.4617G>C
n.4600G>C
dbSNP
12g.45852592G=CA2033475689ARID2c.4469G= (p.Gly1490=)
c.678G=
c.4390G=
c.4022G= (p.Gly1341=)
c.3299G= (p.Gly1100=)
c.293G= (p.Gly98=)
n.3760G=
c.2837G= (p.Gly946=)
n.4617G=
n.4600G=
12g.45852592G>TCA384491799ARID2c.4469G>T (p.Gly1490Val)
c.678G>T
c.4390G>T
c.4022G>T (p.Gly1341Val)
c.3299G>T (p.Gly1100Val)
c.293G>T (p.Gly98Val)
n.3760G>T
c.2837G>T (p.Gly946Val)
n.4617G>T
n.4600G>T
dbSNP gnomAD v4
12g.45852593A=CA2033475690ARID2c.4470A= (p.Gly1490=)
c.679A=
c.4391A=
c.4023A= (p.Gly1341=)
c.3300A= (p.Gly1100=)
c.294A= (p.Gly98=)
n.3761A=
c.2838A= (p.Gly946=)
n.4618A=
n.4601A=
12g.45852593A>CCA479693842ARID2c.4470A>C (p.Gly1490=)
c.679A>C
c.4391A>C
c.4023A>C (p.Gly1341=)
c.3300A>C (p.Gly1100=)
c.294A>C (p.Gly98=)
n.3761A>C
c.2838A>C (p.Gly946=)
n.4618A>C
n.4601A>C
12g.45852593A>GCA479693843ARID2c.4470A>G (p.Gly1490=)
c.679A>G
c.4391A>G
c.4023A>G (p.Gly1341=)
c.3300A>G (p.Gly1100=)
c.294A>G (p.Gly98=)
n.3761A>G
c.2838A>G (p.Gly946=)
n.4618A>G
n.4601A>G
dbSNP gnomAD v4
12g.45852593A>TCA479693844ARID2c.4470A>T (p.Gly1490=)
c.679A>T
c.4391A>T
c.4023A>T (p.Gly1341=)
c.3300A>T (p.Gly1100=)
c.294A>T (p.Gly98=)
n.3761A>T
c.2838A>T (p.Gly946=)
n.4618A>T
n.4601A>T
dbSNP
12g.45852594T>ACA384491800ARID2c.4471T>A (p.Ser1491Thr)
c.680T>A
c.4392T>A
c.4024T>A (p.Ser1342Thr)
c.3301T>A (p.Ser1101Thr)
c.295T>A (p.Ser99Thr)
n.3762T>A
c.2839T>A (p.Ser947Thr)
n.4619T>A
n.4602T>A
dbSNP
12g.45852594T>CCA384491801ARID2c.4471T>C (p.Ser1491Pro)
c.680T>C
c.4392T>C
c.4024T>C (p.Ser1342Pro)
c.3301T>C (p.Ser1101Pro)
c.295T>C (p.Ser99Pro)
n.3762T>C
c.2839T>C (p.Ser947Pro)
n.4619T>C
n.4602T>C
dbSNP
12g.45852594T>GCA384491802ARID2c.4471T>G (p.Ser1491Ala)
c.680T>G
c.4392T>G
c.4024T>G (p.Ser1342Ala)
c.3301T>G (p.Ser1101Ala)
c.295T>G (p.Ser99Ala)
n.3762T>G
c.2839T>G (p.Ser947Ala)
n.4619T>G
n.4602T>G
dbSNP
12g.45852595C>ACA384491805ARID2c.4472C>A (p.Ser1491Ter)
c.681C>A
c.4393C>A
c.4025C>A (p.Ser1342Ter)
c.3302C>A (p.Ser1101Ter)
c.296C>A (p.Ser99Ter)
n.3763C>A
c.2840C>A (p.Ser947Ter)
n.4620C>A
n.4603C>A
12g.45852595C>GCA384491803ARID2c.4472C>G (p.Ser1491Ter)
c.681C>G
c.4393C>G
c.4025C>G (p.Ser1342Ter)
c.3302C>G (p.Ser1101Ter)
c.296C>G (p.Ser99Ter)
n.3763C>G
c.2840C>G (p.Ser947Ter)
n.4620C>G
n.4603C>G
12g.45852595C>TCA384491804ARID2c.4472C>T (p.Ser1491Leu)
c.681C>T
c.4393C>T
c.4025C>T (p.Ser1342Leu)
c.3302C>T (p.Ser1101Leu)
c.296C>T (p.Ser99Leu)
n.3763C>T
c.2840C>T (p.Ser947Leu)
n.4620C>T
n.4603C>T
dbSNP
12g.45852596A>CCA479693846ARID2c.4473A>C (p.Ser1491=)
c.682A>C
c.4394A>C
c.4026A>C (p.Ser1342=)
c.3303A>C (p.Ser1101=)
c.297A>C (p.Ser99=)
n.3764A>C
c.2841A>C (p.Ser947=)
n.4621A>C
n.4604A>C
12g.45852596A>GCA479693847ARID2c.4473A>G (p.Ser1491=)
c.682A>G
c.4394A>G
c.4026A>G (p.Ser1342=)
c.3303A>G (p.Ser1101=)
c.297A>G (p.Ser99=)
n.3764A>G
c.2841A>G (p.Ser947=)
n.4621A>G
n.4604A>G
gnomAD v4
12g.45852596A>TCA479693845ARID2c.4473A>T (p.Ser1491=)
c.682A>T
c.4394A>T
c.4026A>T (p.Ser1342=)
c.3303A>T (p.Ser1101=)
c.297A>T (p.Ser99=)
n.3764A>T
c.2841A>T (p.Ser947=)
n.4621A>T
n.4604A>T
dbSNP
12g.45852597A=CA2033475691ARID2c.4474A= (p.Lys1492=)
c.683A=
c.4395A=
c.4027A= (p.Lys1343=)
c.3304A= (p.Lys1102=)
c.298A= (p.Lys100=)
n.3765A=
c.2842A= (p.Lys948=)
n.4622A=
n.4605A=
12g.45852597A>CCA384491806ARID2c.4474A>C (p.Lys1492Gln)
c.683A>C
c.4395A>C
c.4027A>C (p.Lys1343Gln)
c.3304A>C (p.Lys1102Gln)
c.298A>C (p.Lys100Gln)
n.3765A>C
c.2842A>C (p.Lys948Gln)
n.4622A>C
n.4605A>C
dbSNP
12g.45852597A>GCA6526668ARID2c.4474A>G (p.Lys1492Glu)
c.683A>G
c.4395A>G
c.4027A>G (p.Lys1343Glu)
c.3304A>G (p.Lys1102Glu)
c.298A>G (p.Lys100Glu)
n.3765A>G
c.2842A>G (p.Lys948Glu)
n.4622A>G
n.4605A>G
dbSNP ExAC gnomAD v3 gnomAD v4
12g.45852597A>TCA384491807ARID2c.4474A>T (p.Lys1492Ter)
c.683A>T
c.4395A>T
c.4027A>T (p.Lys1343Ter)
c.3304A>T (p.Lys1102Ter)
c.298A>T (p.Lys100Ter)
n.3765A>T
c.2842A>T (p.Lys948Ter)
n.4622A>T
n.4605A>T
dbSNP
12g.45852598A=CA2033475692ARID2c.4475A= (p.Lys1492=)
c.684A=
c.4396A=
c.4028A= (p.Lys1343=)
c.3305A= (p.Lys1102=)
c.299A= (p.Lys100=)
n.3766A=
c.2843A= (p.Lys948=)
n.4623A=
n.4606A=
12g.45852598A>CCA384491808ARID2c.4475A>C (p.Lys1492Thr)
c.684A>C
c.4396A>C
c.4028A>C (p.Lys1343Thr)
c.3305A>C (p.Lys1102Thr)
c.299A>C (p.Lys100Thr)
n.3766A>C
c.2843A>C (p.Lys948Thr)
n.4623A>C
n.4606A>C
dbSNP gnomAD v3 gnomAD v4
12g.45852598A>GCA384491809ARID2c.4475A>G (p.Lys1492Arg)
c.684A>G
c.4396A>G
c.4028A>G (p.Lys1343Arg)
c.3305A>G (p.Lys1102Arg)
c.299A>G (p.Lys100Arg)
n.3766A>G
c.2843A>G (p.Lys948Arg)
n.4623A>G
n.4606A>G
dbSNP
12g.45852598A>TCA384491810ARID2c.4475A>T (p.Lys1492Ile)
c.684A>T
c.4396A>T
c.4028A>T (p.Lys1343Ile)
c.3305A>T (p.Lys1102Ile)
c.299A>T (p.Lys100Ile)
n.3766A>T
c.2843A>T (p.Lys948Ile)
n.4623A>T
n.4606A>T
dbSNP
12g.45852599A>CCA384491811ARID2c.4476A>C (p.Lys1492Asn)
c.685A>C
c.4397A>C
c.4029A>C (p.Lys1343Asn)
c.3306A>C (p.Lys1102Asn)
c.300A>C (p.Lys100Asn)
n.3767A>C
c.2844A>C (p.Lys948Asn)
n.4624A>C
n.4607A>C
12g.45852599A>GCA479693848ARID2c.4476A>G (p.Lys1492=)
c.685A>G
c.4397A>G
c.4029A>G (p.Lys1343=)
c.3306A>G (p.Lys1102=)
c.300A>G (p.Lys100=)
n.3767A>G
c.2844A>G (p.Lys948=)
n.4624A>G
n.4607A>G
dbSNP
12g.45852599A>TCA384491812ARID2c.4476A>T (p.Lys1492Asn)
c.685A>T
c.4397A>T
c.4029A>T (p.Lys1343Asn)
c.3306A>T (p.Lys1102Asn)
c.300A>T (p.Lys100Asn)
n.3767A>T
c.2844A>T (p.Lys948Asn)
n.4624A>T
n.4607A>T
dbSNP
12g.45852600G>ACA384491813ARID2c.4477G>A (p.Val1493Ile)
c.686G>A
c.4398G>A
c.4030G>A (p.Val1344Ile)
c.3307G>A (p.Val1103Ile)
c.301G>A (p.Val101Ile)
n.3768G>A
c.2845G>A (p.Val949Ile)
n.4625G>A
n.4608G>A
dbSNP
12g.45852600G>CCA384491814ARID2c.4477G>C (p.Val1493Leu)
c.686G>C
c.4398G>C
c.4030G>C (p.Val1344Leu)
c.3307G>C (p.Val1103Leu)
c.301G>C (p.Val101Leu)
n.3768G>C
c.2845G>C (p.Val949Leu)
n.4625G>C
n.4608G>C
dbSNP
12g.45852600G>TCA384491815ARID2c.4477G>T (p.Val1493Leu)
c.686G>T
c.4398G>T
c.4030G>T (p.Val1344Leu)
c.3307G>T (p.Val1103Leu)
c.301G>T (p.Val101Leu)
n.3768G>T
c.2845G>T (p.Val949Leu)
n.4625G>T
n.4608G>T
dbSNP
12g.45852601T>ACA384491817ARID2c.4478T>A (p.Val1493Glu)
c.687T>A
c.4399T>A
c.4031T>A (p.Val1344Glu)
c.3308T>A (p.Val1103Glu)
c.302T>A (p.Val101Glu)
n.3769T>A
c.2846T>A (p.Val949Glu)
n.4626T>A
n.4609T>A
dbSNP gnomAD v3 gnomAD v4
12g.45852601T>CCA384491818ARID2c.4478T>C (p.Val1493Ala)
c.687T>C
c.4399T>C
c.4031T>C (p.Val1344Ala)
c.3308T>C (p.Val1103Ala)
c.302T>C (p.Val101Ala)
n.3769T>C
c.2846T>C (p.Val949Ala)
n.4626T>C
n.4609T>C
dbSNP
12g.45852601T>GCA384491816ARID2c.4478T>G (p.Val1493Gly)
c.687T>G
c.4399T>G
c.4031T>G (p.Val1344Gly)
c.3308T>G (p.Val1103Gly)
c.302T>G (p.Val101Gly)
n.3769T>G
c.2846T>G (p.Val949Gly)
n.4626T>G
n.4609T>G
dbSNP
12g.45852601T=CA2033475693ARID2c.4478T= (p.Val1493=)
c.687T=
c.4399T=
c.4031T= (p.Val1344=)
c.3308T= (p.Val1103=)
c.302T= (p.Val101=)
n.3769T=
c.2846T= (p.Val949=)
n.4626T=
n.4609T=
12g.45852602A>CCA479693850ARID2c.4479A>C (p.Val1493=)
c.688A>C
c.4400A>C
c.4032A>C (p.Val1344=)
c.3309A>C (p.Val1103=)
c.303A>C (p.Val101=)
n.3770A>C
c.2847A>C (p.Val949=)
n.4627A>C
n.4610A>C
dbSNP
12g.45852602A>GCA479693851ARID2c.4479A>G (p.Val1493=)
c.688A>G
c.4400A>G
c.4032A>G (p.Val1344=)
c.3309A>G (p.Val1103=)
c.303A>G (p.Val101=)
n.3770A>G
c.2847A>G (p.Val949=)
n.4627A>G
n.4610A>G
gnomAD v4
12g.45852602A>TCA479693849ARID2c.4479A>T (p.Val1493=)
c.688A>T
c.4400A>T
c.4032A>T (p.Val1344=)
c.3309A>T (p.Val1103=)
c.303A>T (p.Val101=)
n.3770A>T
c.2847A>T (p.Val949=)
n.4627A>T
n.4610A>T
dbSNP
12g.45852603T>ACA384491821ARID2c.4480T>A (p.Ser1494Thr)
c.689T>A
c.4401T>A
c.4033T>A (p.Ser1345Thr)
c.3310T>A (p.Ser1104Thr)
c.304T>A (p.Ser102Thr)
n.3771T>A
c.2848T>A (p.Ser950Thr)
n.4628T>A
n.4611T>A
12g.45852603T>CCA384491819ARID2c.4480T>C (p.Ser1494Pro)
c.689T>C
c.4401T>C
c.4033T>C (p.Ser1345Pro)
c.3310T>C (p.Ser1104Pro)
c.304T>C (p.Ser102Pro)
n.3771T>C
c.2848T>C (p.Ser950Pro)
n.4628T>C
n.4611T>C
dbSNP
12g.45852603T>GCA384491820ARID2c.4480T>G (p.Ser1494Ala)
c.689T>G
c.4401T>G
c.4033T>G (p.Ser1345Ala)
c.3310T>G (p.Ser1104Ala)
c.304T>G (p.Ser102Ala)
n.3771T>G
c.2848T>G (p.Ser950Ala)
n.4628T>G
n.4611T>G
12g.45852604C>ACA384491822ARID2c.4481C>A (p.Ser1494Tyr)
c.690C>A
c.4402C>A
c.4034C>A (p.Ser1345Tyr)
c.3311C>A (p.Ser1104Tyr)
c.305C>A (p.Ser102Tyr)
n.3772C>A
c.2849C>A (p.Ser950Tyr)
n.4629C>A
n.4612C>A
dbSNP
12g.45852604C=CA2033475694ARID2c.4481C= (p.Ser1494=)
c.690C=
c.4402C=
c.4034C= (p.Ser1345=)
c.3311C= (p.Ser1104=)
c.305C= (p.Ser102=)
n.3772C=
c.2849C= (p.Ser950=)
n.4629C=
n.4612C=
12g.45852604C>GCA384491823ARID2c.4481C>G (p.Ser1494Cys)
c.690C>G
c.4402C>G
c.4034C>G (p.Ser1345Cys)
c.3311C>G (p.Ser1104Cys)
c.305C>G (p.Ser102Cys)
n.3772C>G
c.2849C>G (p.Ser950Cys)
n.4629C>G
n.4612C>G
dbSNP
12g.45852604C>TCA384491824ARID2c.4481C>T (p.Ser1494Phe)
c.690C>T
c.4402C>T
c.4034C>T (p.Ser1345Phe)
c.3311C>T (p.Ser1104Phe)
c.305C>T (p.Ser102Phe)
n.3772C>T
c.2849C>T (p.Ser950Phe)
n.4629C>T
n.4612C>T
dbSNP gnomAD v3 gnomAD v4
12g.45852605C>ACA479693854ARID2c.4482C>A (p.Ser1494=)
c.691C>A
c.4403C>A
c.4035C>A (p.Ser1345=)
c.3312C>A (p.Ser1104=)
c.306C>A (p.Ser102=)
n.3773C>A
c.2850C>A (p.Ser950=)
n.4630C>A
n.4613C>A
dbSNP
12g.45852605C>GCA479693853ARID2c.4482C>G (p.Ser1494=)
c.691C>G
c.4403C>G
c.4035C>G (p.Ser1345=)
c.3312C>G (p.Ser1104=)
c.306C>G (p.Ser102=)
n.3773C>G
c.2850C>G (p.Ser950=)
n.4630C>G
n.4613C>G
dbSNP
12g.45852605C>TCA479693852ARID2c.4482C>T (p.Ser1494=)
c.691C>T
c.4403C>T
c.4035C>T (p.Ser1345=)
c.3312C>T (p.Ser1104=)
c.306C>T (p.Ser102=)
n.3773C>T
c.2850C>T (p.Ser950=)
n.4630C>T
n.4613C>T
dbSNP
12g.45852606C>ACA384491825ARID2c.4483C>A (p.His1495Asn)
c.692C>A
c.4404C>A
c.4036C>A (p.His1346Asn)
c.3313C>A (p.His1105Asn)
c.307C>A (p.His103Asn)
n.3774C>A
c.2851C>A (p.His951Asn)
n.4631C>A
n.4614C>A
dbSNP
12g.45852606C>GCA384491826ARID2c.4483C>G (p.His1495Asp)
c.692C>G
c.4404C>G
c.4036C>G (p.His1346Asp)
c.3313C>G (p.His1105Asp)
c.307C>G (p.His103Asp)
n.3774C>G
c.2851C>G (p.His951Asp)
n.4631C>G
n.4614C>G
dbSNP
12g.45852606C>TCA384491827ARID2c.4483C>T (p.His1495Tyr)
c.692C>T
c.4404C>T
c.4036C>T (p.His1346Tyr)
c.3313C>T (p.His1105Tyr)
c.307C>T (p.His103Tyr)
n.3774C>T
c.2851C>T (p.His951Tyr)
n.4631C>T
n.4614C>T
dbSNP gnomAD v4
12g.45852607A=CA2033475695ARID2c.4484A= (p.His1495=)
c.693A=
c.4405A=
c.4037A= (p.His1346=)
c.3314A= (p.His1105=)
c.308A= (p.His103=)
n.3775A=
c.2852A= (p.His951=)
n.4632A=
n.4615A=
12g.45852607A>CCA384491828ARID2c.4484A>C (p.His1495Pro)
c.693A>C
c.4405A>C
c.4037A>C (p.His1346Pro)
c.3314A>C (p.His1105Pro)
c.308A>C (p.His103Pro)
n.3775A>C
c.2852A>C (p.His951Pro)
n.4632A>C
n.4615A>C
dbSNP
12g.45852607A>GCA384491829ARID2c.4484A>G (p.His1495Arg)
c.693A>G
c.4405A>G
c.4037A>G (p.His1346Arg)
c.3314A>G (p.His1105Arg)
c.308A>G (p.His103Arg)
n.3775A>G
c.2852A>G (p.His951Arg)
n.4632A>G
n.4615A>G
dbSNP gnomAD v3 gnomAD v4
12g.45852607A>TCA384491830ARID2c.4484A>T (p.His1495Leu)
c.693A>T
c.4405A>T
c.4037A>T (p.His1346Leu)
c.3314A>T (p.His1105Leu)
c.308A>T (p.His103Leu)
n.3775A>T
c.2852A>T (p.His951Leu)
n.4632A>T
n.4615A>T
dbSNP gnomAD v4
12g.45852608T>ACA384491831ARID2c.4485T>A (p.His1495Gln)
c.694T>A
c.4406T>A
c.4038T>A (p.His1346Gln)
c.3315T>A (p.His1105Gln)
c.309T>A (p.His103Gln)
n.3776T>A
c.2853T>A (p.His951Gln)
n.4633T>A
n.4616T>A
dbSNP
12g.45852608T>CCA479693855ARID2c.4485T>C (p.His1495=)
c.694T>C
c.4406T>C
c.4038T>C (p.His1346=)
c.3315T>C (p.His1105=)
c.309T>C (p.His103=)
n.3776T>C
c.2853T>C (p.His951=)
n.4633T>C
n.4616T>C
dbSNP
12g.45852608T>GCA384491832ARID2c.4485T>G (p.His1495Gln)
c.694T>G
c.4406T>G
c.4038T>G (p.His1346Gln)
c.3315T>G (p.His1105Gln)
c.309T>G (p.His103Gln)
n.3776T>G
c.2853T>G (p.His951Gln)
n.4633T>G
n.4616T>G
12g.45852609T>ACA384491835ARID2c.4486T>A (p.Ser1496Thr)
c.695T>A
c.4407T>A
c.4039T>A (p.Ser1347Thr)
c.3316T>A (p.Ser1106Thr)
c.310T>A (p.Ser104Thr)
n.3777T>A
c.2854T>A (p.Ser952Thr)
n.4634T>A
n.4617T>A
dbSNP
12g.45852609T>CCA384491833ARID2c.4486T>C (p.Ser1496Pro)
c.695T>C
c.4407T>C
c.4039T>C (p.Ser1347Pro)
c.3316T>C (p.Ser1106Pro)
c.310T>C (p.Ser104Pro)
n.3777T>C
c.2854T>C (p.Ser952Pro)
n.4634T>C
n.4617T>C
12g.45852609T>GCA384491834ARID2c.4486T>G (p.Ser1496Ala)
c.695T>G
c.4407T>G
c.4039T>G (p.Ser1347Ala)
c.3316T>G (p.Ser1106Ala)
c.310T>G (p.Ser104Ala)
n.3777T>G
c.2854T>G (p.Ser952Ala)
n.4634T>G
n.4617T>G
12g.45852610C>ACA384491836ARID2c.4487C>A (p.Ser1496Tyr)
c.696C>A
c.4408C>A
c.4040C>A (p.Ser1347Tyr)
c.3317C>A (p.Ser1106Tyr)
c.311C>A (p.Ser104Tyr)
n.3778C>A
c.2855C>A (p.Ser952Tyr)
n.4635C>A
n.4618C>A
dbSNP
12g.45852610C>GCA384491837ARID2c.4487C>G (p.Ser1496Cys)
c.696C>G
c.4408C>G
c.4040C>G (p.Ser1347Cys)
c.3317C>G (p.Ser1106Cys)
c.311C>G (p.Ser104Cys)
n.3778C>G
c.2855C>G (p.Ser952Cys)
n.4635C>G
n.4618C>G
dbSNP gnomAD v4
12g.45852610C>TCA384491838ARID2c.4487C>T (p.Ser1496Phe)
c.696C>T
c.4408C>T
c.4040C>T (p.Ser1347Phe)
c.3317C>T (p.Ser1106Phe)
c.311C>T (p.Ser104Phe)
n.3778C>T
c.2855C>T (p.Ser952Phe)
n.4635C>T
n.4618C>T
dbSNP COSMIC
12g.45852611T>ACA479693856ARID2c.4488T>A (p.Ser1496=)
c.697T>A
c.4409T>A
c.4041T>A (p.Ser1347=)
c.3318T>A (p.Ser1106=)
c.312T>A (p.Ser104=)
n.3779T>A
c.2856T>A (p.Ser952=)
n.4636T>A
n.4619T>A
dbSNP
12g.45852611T>CCA479693857ARID2c.4488T>C (p.Ser1496=)
c.697T>C
c.4409T>C
c.4041T>C (p.Ser1347=)
c.3318T>C (p.Ser1106=)
c.312T>C (p.Ser104=)
n.3779T>C
c.2856T>C (p.Ser952=)
n.4636T>C
n.4619T>C
dbSNP
12g.45852611T>GCA479693858ARID2c.4488T>G (p.Ser1496=)
c.697T>G
c.4409T>G
c.4041T>G (p.Ser1347=)
c.3318T>G (p.Ser1106=)
c.312T>G (p.Ser104=)
n.3779T>G
c.2856T>G (p.Ser952=)
n.4636T>G
n.4619T>G
12g.45852611_45852612insACCA2515753600ARID2c.4488_4489insAC (p.Pro1497ThrfsTer20)
c.697_698insAC
c.4409_4410insAC
c.4041_4042insAC (p.Pro1348ThrfsTer20)
c.3318_3319insAC (p.Pro1107ThrfsTer20)
c.312_313insAC (p.Pro105ThrfsTer20)
n.3779_3780insAC
c.2856_2857insAC (p.Pro953ThrfsTer20)
n.4636_4637insAC
n.4619_4620insAC
12g.45852612C>ACA384491839ARID2c.4489C>A (p.Pro1497Thr)
c.698C>A
c.4410C>A
c.4042C>A (p.Pro1348Thr)
c.3319C>A (p.Pro1107Thr)
c.313C>A (p.Pro105Thr)
n.3780C>A
c.2857C>A (p.Pro953Thr)
n.4637C>A
n.4620C>A
dbSNP
12g.45852612C=CA2033475696ARID2c.4489C= (p.Pro1497=)
c.698C=
c.4410C=
c.4042C= (p.Pro1348=)
c.3319C= (p.Pro1107=)
c.313C= (p.Pro105=)
n.3780C=
c.2857C= (p.Pro953=)
n.4637C=
n.4620C=
12g.45852612C>GCA384491840ARID2c.4489C>G (p.Pro1497Ala)
c.698C>G
c.4410C>G
c.4042C>G (p.Pro1348Ala)
c.3319C>G (p.Pro1107Ala)
c.313C>G (p.Pro105Ala)
n.3780C>G
c.2857C>G (p.Pro953Ala)
n.4637C>G
n.4620C>G
dbSNP
12g.45852612C>TCA6526669ARID2c.4489C>T (p.Pro1497Ser)
c.698C>T
c.4410C>T
c.4042C>T (p.Pro1348Ser)
c.3319C>T (p.Pro1107Ser)
c.313C>T (p.Pro105Ser)
n.3780C>T
c.2857C>T (p.Pro953Ser)
n.4637C>T
n.4620C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852613C>ACA384491841ARID2c.4490C>A (p.Pro1497His)
c.699C>A
c.4411C>A
c.4043C>A (p.Pro1348His)
c.3320C>A (p.Pro1107His)
c.314C>A (p.Pro105His)
n.3781C>A
c.2858C>A (p.Pro953His)
n.4638C>A
n.4621C>A
dbSNP
12g.45852613C=CA2033475697ARID2c.4490C= (p.Pro1497=)
c.699C=
c.4411C=
c.4043C= (p.Pro1348=)
c.3320C= (p.Pro1107=)
c.314C= (p.Pro105=)
n.3781C=
c.2858C= (p.Pro953=)
n.4638C=
n.4621C=
12g.45852613C>GCA384491842ARID2c.4490C>G (p.Pro1497Arg)
c.699C>G
c.4411C>G
c.4043C>G (p.Pro1348Arg)
c.3320C>G (p.Pro1107Arg)
c.314C>G (p.Pro105Arg)
n.3781C>G
c.2858C>G (p.Pro953Arg)
n.4638C>G
n.4621C>G
dbSNP
12g.45852613C>TCA384491843ARID2c.4490C>T (p.Pro1497Leu)
c.699C>T
c.4411C>T
c.4043C>T (p.Pro1348Leu)
c.3320C>T (p.Pro1107Leu)
c.314C>T (p.Pro105Leu)
n.3781C>T
c.2858C>T (p.Pro953Leu)
n.4638C>T
n.4621C>T
dbSNP gnomAD v3 gnomAD v4
12g.45852614T>ACA479693859ARID2c.4491T>A (p.Pro1497=)
c.700T>A
c.4412T>A
c.4044T>A (p.Pro1348=)
c.3321T>A (p.Pro1107=)
c.315T>A (p.Pro105=)
n.3782T>A
c.2859T>A (p.Pro953=)
n.4639T>A
n.4622T>A
dbSNP gnomAD v4
12g.45852614T>CCA479693860ARID2c.4491T>C (p.Pro1497=)
c.700T>C
c.4412T>C
c.4044T>C (p.Pro1348=)
c.3321T>C (p.Pro1107=)
c.315T>C (p.Pro105=)
n.3782T>C
c.2859T>C (p.Pro953=)
n.4639T>C
n.4622T>C
12g.45852614T>GCA479693861ARID2c.4491T>G (p.Pro1497=)
c.700T>G
c.4412T>G
c.4044T>G (p.Pro1348=)
c.3321T>G (p.Pro1107=)
c.315T>G (p.Pro105=)
n.3782T>G
c.2859T>G (p.Pro953=)
n.4639T>G
n.4622T>G
12g.45852614T=CA2033475698ARID2c.4491T= (p.Pro1497=)
c.700T=
c.4412T=
c.4044T= (p.Pro1348=)
c.3321T= (p.Pro1107=)
c.315T= (p.Pro105=)
n.3782T=
c.2859T= (p.Pro953=)
n.4639T=
n.4622T=
12g.45852615G>ACA156968ARID2c.4492G>A (p.Ala1498Thr)
c.701G>A
c.4413G>A
c.4045G>A (p.Ala1349Thr)
c.3322G>A (p.Ala1108Thr)
c.316G>A (p.Ala106Thr)
n.3783G>A
c.2860G>A (p.Ala954Thr)
n.4640G>A
n.4623G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852615G>CCA384491844ARID2c.4492G>C (p.Ala1498Pro)
c.701G>C
c.4413G>C
c.4045G>C (p.Ala1349Pro)
c.3322G>C (p.Ala1108Pro)
c.316G>C (p.Ala106Pro)
n.3783G>C
c.2860G>C (p.Ala954Pro)
n.4640G>C
n.4623G>C
dbSNP
12g.45852615G=CA2033475699ARID2c.4492G= (p.Ala1498=)
c.701G=
c.4413G=
c.4045G= (p.Ala1349=)
c.3322G= (p.Ala1108=)
c.316G= (p.Ala106=)
n.3783G=
c.2860G= (p.Ala954=)
n.4640G=
n.4623G=
12g.45852615G>TCA384491845ARID2c.4492G>T (p.Ala1498Ser)
c.701G>T
c.4413G>T
c.4045G>T (p.Ala1349Ser)
c.3322G>T (p.Ala1108Ser)
c.316G>T (p.Ala106Ser)
n.3783G>T
c.2860G>T (p.Ala954Ser)
n.4640G>T
n.4623G>T
dbSNP gnomAD v4
12g.45852616C>ACA384491847ARID2c.4493C>A (p.Ala1498Asp)
c.702C>A
c.4414C>A
c.4046C>A (p.Ala1349Asp)
c.3323C>A (p.Ala1108Asp)
c.317C>A (p.Ala106Asp)
n.3784C>A
c.2861C>A (p.Ala954Asp)
n.4641C>A
n.4624C>A
dbSNP
12g.45852616C=CA2033475700ARID2c.4493C= (p.Ala1498=)
c.702C=
c.4414C=
c.4046C= (p.Ala1349=)
c.3323C= (p.Ala1108=)
c.317C= (p.Ala106=)
n.3784C=
c.2861C= (p.Ala954=)
n.4641C=
n.4624C=
12g.45852616C>GCA384491846ARID2c.4493C>G (p.Ala1498Gly)
c.702C>G
c.4414C>G
c.4046C>G (p.Ala1349Gly)
c.3323C>G (p.Ala1108Gly)
c.317C>G (p.Ala106Gly)
n.3784C>G
c.2861C>G (p.Ala954Gly)
n.4641C>G
n.4624C>G
dbSNP
12g.45852616C>TCA6526670ARID2c.4493C>T (p.Ala1498Val)
c.702C>T
c.4414C>T
c.4046C>T (p.Ala1349Val)
c.3323C>T (p.Ala1108Val)
c.317C>T (p.Ala106Val)
n.3784C>T
c.2861C>T (p.Ala954Val)
n.4641C>T
n.4624C>T
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
12g.45852616_45852620delCA2507655013ARID2c.4493_4497del (p.Ala1498ValfsTer3)
c.702_706del
c.4414_4418del
c.4046_4050del (p.Ala1349ValfsTer3)
c.3323_3327del (p.Ala1108ValfsTer3)
c.317_321del (p.Ala106ValfsTer3)
n.3784_3788del
c.2861_2865del (p.Ala954ValfsTer3)
n.4641_4645del
n.4624_4628del
12g.45852617C>ACA479693862ARID2c.4494C>A (p.Ala1498=)
c.703C>A
c.4415C>A
c.4047C>A (p.Ala1349=)
c.3324C>A (p.Ala1108=)
c.318C>A (p.Ala106=)
n.3785C>A
c.2862C>A (p.Ala954=)
n.4642C>A
n.4625C>A
dbSNP
12g.45852617C=CA2033475701ARID2c.4494C= (p.Ala1498=)
c.703C=
c.4415C=
c.4047C= (p.Ala1349=)
c.3324C= (p.Ala1108=)
c.318C= (p.Ala106=)
n.3785C=
c.2862C= (p.Ala954=)
n.4642C=
n.4625C=
12g.45852617C>GCA479693863ARID2c.4494C>G (p.Ala1498=)
c.703C>G
c.4415C>G
c.4047C>G (p.Ala1349=)
c.3324C>G (p.Ala1108=)
c.318C>G (p.Ala106=)
n.3785C>G
c.2862C>G (p.Ala954=)
n.4642C>G
n.4625C>G
dbSNP
12g.45852617C>TCA479693864ARID2c.4494C>T (p.Ala1498=)
c.703C>T
c.4415C>T
c.4047C>T (p.Ala1349=)
c.3324C>T (p.Ala1108=)
c.318C>T (p.Ala106=)
n.3785C>T
c.2862C>T (p.Ala954=)
n.4642C>T
n.4625C>T
dbSNP gnomAD v4
12g.45852618C>ACA384491848ARID2c.4495C>A (p.Leu1499Ile)
c.704C>A
c.4416C>A
c.4048C>A (p.Leu1350Ile)
c.3325C>A (p.Leu1109Ile)
c.319C>A (p.Leu107Ile)
n.3786C>A
c.2863C>A (p.Leu955Ile)
n.4643C>A
n.4626C>A
dbSNP
12g.45852618C=CA2033475702ARID2c.4495C= (p.Leu1499=)
c.704C=
c.4416C=
c.4048C= (p.Leu1350=)
c.3325C= (p.Leu1109=)
c.319C= (p.Leu107=)
n.3786C=
c.2863C= (p.Leu955=)
n.4643C=
n.4626C=
12g.45852618C>GCA384491849ARID2c.4495C>G (p.Leu1499Val)
c.704C>G
c.4416C>G
c.4048C>G (p.Leu1350Val)
c.3325C>G (p.Leu1109Val)
c.319C>G (p.Leu107Val)
n.3786C>G
c.2863C>G (p.Leu955Val)
n.4643C>G
n.4626C>G
dbSNP gnomAD v4
12g.45852618C>TCA6526671ARID2c.4495C>T (p.Leu1499=)
c.704C>T
c.4416C>T
c.4048C>T (p.Leu1350=)
c.3325C>T (p.Leu1109=)
c.319C>T (p.Leu107=)
n.3786C>T
c.2863C>T (p.Leu955=)
n.4643C>T
n.4626C>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852619T>ACA384491850ARID2c.4496T>A (p.Leu1499Gln)
c.705T>A
c.4417T>A
c.4049T>A (p.Leu1350Gln)
c.3326T>A (p.Leu1109Gln)
c.320T>A (p.Leu107Gln)
n.3787T>A
c.2864T>A (p.Leu955Gln)
n.4644T>A
n.4627T>A
dbSNP
12g.45852619T>CCA384491851ARID2c.4496T>C (p.Leu1499Pro)
c.705T>C
c.4417T>C
c.4049T>C (p.Leu1350Pro)
c.3326T>C (p.Leu1109Pro)
c.320T>C (p.Leu107Pro)
n.3787T>C
c.2864T>C (p.Leu955Pro)
n.4644T>C
n.4627T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.45852619T>GCA384491852ARID2c.4496T>G (p.Leu1499Arg)
c.705T>G
c.4417T>G
c.4049T>G (p.Leu1350Arg)
c.3326T>G (p.Leu1109Arg)
c.320T>G (p.Leu107Arg)
n.3787T>G
c.2864T>G (p.Leu955Arg)
n.4644T>G
n.4627T>G
ClinVar
12g.45852619T=CA2033475703ARID2c.4496T= (p.Leu1499=)
c.705T=
c.4417T=
c.4049T= (p.Leu1350=)
c.3326T= (p.Leu1109=)
c.320T= (p.Leu107=)
n.3787T=
c.2864T= (p.Leu955=)
n.4644T=
n.4627T=
12g.45852620A=CA2033475704ARID2c.4497A= (p.Leu1499=)
c.706A=
c.4418A=
c.4050A= (p.Leu1350=)
c.3327A= (p.Leu1109=)
c.321A= (p.Leu107=)
n.3788A=
c.2865A= (p.Leu955=)
n.4645A=
n.4628A=
12g.45852620A>CCA479693865ARID2c.4497A>C (p.Leu1499=)
c.706A>C
c.4418A>C
c.4050A>C (p.Leu1350=)
c.3327A>C (p.Leu1109=)
c.321A>C (p.Leu107=)
n.3788A>C
c.2865A>C (p.Leu955=)
n.4645A>C
n.4628A>C
dbSNP
12g.45852620A>GCA6526672ARID2c.4497A>G (p.Leu1499=)
c.706A>G
c.4418A>G
c.4050A>G (p.Leu1350=)
c.3327A>G (p.Leu1109=)
c.321A>G (p.Leu107=)
n.3788A>G
c.2865A>G (p.Leu955=)
n.4645A>G
n.4628A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852620A>TCA479693866ARID2c.4497A>T (p.Leu1499=)
c.706A>T
c.4418A>T
c.4050A>T (p.Leu1350=)
c.3327A>T (p.Leu1109=)
c.321A>T (p.Leu107=)
n.3788A>T
c.2865A>T (p.Leu955=)
n.4645A>T
n.4628A>T
dbSNP gnomAD v3 gnomAD v4
12g.45852621T>ACA384491853ARID2c.4498T>A (p.Ser1500Thr)
c.707T>A
c.4419T>A
c.4051T>A (p.Ser1351Thr)
c.3328T>A (p.Ser1110Thr)
c.322T>A (p.Ser108Thr)
n.3789T>A
c.2866T>A (p.Ser956Thr)
n.4646T>A
n.4629T>A
dbSNP
12g.45852621T>CCA384491854ARID2c.4498T>C (p.Ser1500Pro)
c.707T>C
c.4419T>C
c.4051T>C (p.Ser1351Pro)
c.3328T>C (p.Ser1110Pro)
c.322T>C (p.Ser108Pro)
n.3789T>C
c.2866T>C (p.Ser956Pro)
n.4646T>C
n.4629T>C
dbSNP gnomAD v4
12g.45852621T>GCA384491855ARID2c.4498T>G (p.Ser1500Ala)
c.707T>G
c.4419T>G
c.4051T>G (p.Ser1351Ala)
c.3328T>G (p.Ser1110Ala)
c.322T>G (p.Ser108Ala)
n.3789T>G
c.2866T>G (p.Ser956Ala)
n.4646T>G
n.4629T>G
12g.45852622C>ACA384491856ARID2c.4499C>A (p.Ser1500Ter)
c.708C>A
c.4420C>A
c.4052C>A (p.Ser1351Ter)
c.3329C>A (p.Ser1110Ter)
c.323C>A (p.Ser108Ter)
n.3790C>A
c.2867C>A (p.Ser956Ter)
n.4647C>A
n.4630C>A
dbSNP
12g.45852622C>GCA384491857ARID2c.4499C>G (p.Ser1500Ter)
c.708C>G
c.4420C>G
c.4052C>G (p.Ser1351Ter)
c.3329C>G (p.Ser1110Ter)
c.323C>G (p.Ser108Ter)
n.3790C>G
c.2867C>G (p.Ser956Ter)
n.4647C>G
n.4630C>G
dbSNP
12g.45852622C>TCA384491858ARID2c.4499C>T (p.Ser1500Leu)
c.708C>T
c.4420C>T
c.4052C>T (p.Ser1351Leu)
c.3329C>T (p.Ser1110Leu)
c.323C>T (p.Ser108Leu)
n.3790C>T
c.2867C>T (p.Ser956Leu)
n.4647C>T
n.4630C>T
dbSNP
12g.45852623A=CA2033475705ARID2c.4500A= (p.Ser1500=)
c.709A=
c.4421A=
c.4053A= (p.Ser1351=)
c.3330A= (p.Ser1110=)
c.324A= (p.Ser108=)
n.3791A=
c.2868A= (p.Ser956=)
n.4648A=
n.4631A=
12g.45852623A>CCA479693869ARID2c.4500A>C (p.Ser1500=)
c.709A>C
c.4421A>C
c.4053A>C (p.Ser1351=)
c.3330A>C (p.Ser1110=)
c.324A>C (p.Ser108=)
n.3791A>C
c.2868A>C (p.Ser956=)
n.4648A>C
n.4631A>C
dbSNP
12g.45852623A>GCA479693868ARID2c.4500A>G (p.Ser1500=)
c.709A>G
c.4421A>G
c.4053A>G (p.Ser1351=)
c.3330A>G (p.Ser1110=)
c.324A>G (p.Ser108=)
n.3791A>G
c.2868A>G (p.Ser956=)
n.4648A>G
n.4631A>G
dbSNP gnomAD v4
12g.45852623A>TCA479693867ARID2c.4500A>T (p.Ser1500=)
c.709A>T
c.4421A>T
c.4053A>T (p.Ser1351=)
c.3330A>T (p.Ser1110=)
c.324A>T (p.Ser108=)
n.3791A>T
c.2868A>T (p.Ser956=)
n.4648A>T
n.4631A>T
dbSNP
12g.45852624T>ACA384491861ARID2c.4501T>A (p.Ser1501Thr)
c.710T>A
c.4422T>A
c.4054T>A (p.Ser1352Thr)
c.3331T>A (p.Ser1111Thr)
c.325T>A (p.Ser109Thr)
n.3792T>A
c.2869T>A (p.Ser957Thr)
n.4649T>A
n.4632T>A
dbSNP
12g.45852624T>CCA384491859ARID2c.4501T>C (p.Ser1501Pro)
c.710T>C
c.4422T>C
c.4054T>C (p.Ser1352Pro)
c.3331T>C (p.Ser1111Pro)
c.325T>C (p.Ser109Pro)
n.3792T>C
c.2869T>C (p.Ser957Pro)
n.4649T>C
n.4632T>C
dbSNP
12g.45852624T>GCA384491860ARID2c.4501T>G (p.Ser1501Ala)
c.710T>G
c.4422T>G
c.4054T>G (p.Ser1352Ala)
c.3331T>G (p.Ser1111Ala)
c.325T>G (p.Ser109Ala)
n.3792T>G
c.2869T>G (p.Ser957Ala)
n.4649T>G
n.4632T>G
12g.45852625C>ACA384491862ARID2c.4502C>A (p.Ser1501Tyr)
c.711C>A
c.4423C>A
c.4055C>A (p.Ser1352Tyr)
c.3332C>A (p.Ser1111Tyr)
c.326C>A (p.Ser109Tyr)
n.3793C>A
c.2870C>A (p.Ser957Tyr)
n.4650C>A
n.4633C>A
dbSNP
12g.45852625C>GCA384491863ARID2c.4502C>G (p.Ser1501Cys)
c.711C>G
c.4423C>G
c.4055C>G (p.Ser1352Cys)
c.3332C>G (p.Ser1111Cys)
c.326C>G (p.Ser109Cys)
n.3793C>G
c.2870C>G (p.Ser957Cys)
n.4650C>G
n.4633C>G
dbSNP
12g.45852625C>TCA384491864ARID2c.4502C>T (p.Ser1501Phe)
c.711C>T
c.4423C>T
c.4055C>T (p.Ser1352Phe)
c.3332C>T (p.Ser1111Phe)
c.326C>T (p.Ser109Phe)
n.3793C>T
c.2870C>T (p.Ser957Phe)
n.4650C>T
n.4633C>T
dbSNP
12g.45852626T>ACA479693871ARID2c.4503T>A (p.Ser1501=)
c.712T>A
c.4424T>A
c.4056T>A (p.Ser1352=)
c.3333T>A (p.Ser1111=)
c.327T>A (p.Ser109=)
n.3794T>A
c.2871T>A (p.Ser957=)
n.4651T>A
n.4634T>A
dbSNP
12g.45852626T>CCA6526673ARID2c.4503T>C (p.Ser1501=)
c.712T>C
c.4424T>C
c.4056T>C (p.Ser1352=)
c.3333T>C (p.Ser1111=)
c.327T>C (p.Ser109=)
n.3794T>C
c.2871T>C (p.Ser957=)
n.4651T>C
n.4634T>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852626T>GCA479693870ARID2c.4503T>G (p.Ser1501=)
c.712T>G
c.4424T>G
c.4056T>G (p.Ser1352=)
c.3333T>G (p.Ser1111=)
c.327T>G (p.Ser109=)
n.3794T>G
c.2871T>G (p.Ser957=)
n.4651T>G
n.4634T>G
dbSNP
12g.45852626T=CA2033475706ARID2c.4503T= (p.Ser1501=)
c.712T=
c.4424T=
c.4056T= (p.Ser1352=)
c.3333T= (p.Ser1111=)
c.327T= (p.Ser109=)
n.3794T=
c.2871T= (p.Ser957=)
n.4651T=
n.4634T=
12g.45852627G>ACA384491865ARID2c.4504G>A (p.Asp1502Asn)
c.713G>A
c.4425G>A
c.4057G>A (p.Asp1353Asn)
c.3334G>A (p.Asp1112Asn)
c.328G>A (p.Asp110Asn)
n.3795G>A
c.2872G>A (p.Asp958Asn)
n.4652G>A
n.4635G>A
dbSNP
12g.45852627G>CCA384491866ARID2c.4504G>C (p.Asp1502His)
c.713G>C
c.4425G>C
c.4057G>C (p.Asp1353His)
c.3334G>C (p.Asp1112His)
c.328G>C (p.Asp110His)
n.3795G>C
c.2872G>C (p.Asp958His)
n.4652G>C
n.4635G>C
dbSNP
12g.45852627G>TCA384491867ARID2c.4504G>T (p.Asp1502Tyr)
c.713G>T
c.4425G>T
c.4057G>T (p.Asp1353Tyr)
c.3334G>T (p.Asp1112Tyr)
c.328G>T (p.Asp110Tyr)
n.3795G>T
c.2872G>T (p.Asp958Tyr)
n.4652G>T
n.4635G>T
dbSNP
12g.45852628A=CA2033475707ARID2c.4505A= (p.Asp1502=)
c.714A=
c.4426A=
c.4058A= (p.Asp1353=)
c.3335A= (p.Asp1112=)
c.329A= (p.Asp110=)
n.3796A=
c.2873A= (p.Asp958=)
n.4653A=
n.4636A=
12g.45852628A>CCA384491868ARID2c.4505A>C (p.Asp1502Ala)
c.714A>C
c.4426A>C
c.4058A>C (p.Asp1353Ala)
c.3335A>C (p.Asp1112Ala)
c.329A>C (p.Asp110Ala)
n.3796A>C
c.2873A>C (p.Asp958Ala)
n.4653A>C
n.4636A>C
dbSNP
12g.45852628A>GCA6526674ARID2c.4505A>G (p.Asp1502Gly)
c.714A>G
c.4426A>G
c.4058A>G (p.Asp1353Gly)
c.3335A>G (p.Asp1112Gly)
c.329A>G (p.Asp110Gly)
n.3796A>G
c.2873A>G (p.Asp958Gly)
n.4653A>G
n.4636A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852628A>TCA384491869ARID2c.4505A>T (p.Asp1502Val)
c.714A>T
c.4426A>T
c.4058A>T (p.Asp1353Val)
c.3335A>T (p.Asp1112Val)
c.329A>T (p.Asp110Val)
n.3796A>T
c.2873A>T (p.Asp958Val)
n.4653A>T
n.4636A>T
dbSNP
12g.45852629C>ACA384491870ARID2c.4506C>A (p.Asp1502Glu)
c.715C>A
c.4427C>A
c.4059C>A (p.Asp1353Glu)
c.3336C>A (p.Asp1112Glu)
c.330C>A (p.Asp110Glu)
n.3797C>A
c.2874C>A (p.Asp958Glu)
n.4654C>A
n.4637C>A
dbSNP
12g.45852629C=CA2033475708ARID2c.4506C= (p.Asp1502=)
c.715C=
c.4427C=
c.4059C= (p.Asp1353=)
c.3336C= (p.Asp1112=)
c.330C= (p.Asp110=)
n.3797C=
c.2874C= (p.Asp958=)
n.4654C=
n.4637C=
12g.45852629C>GCA384491871ARID2c.4506C>G (p.Asp1502Glu)
c.715C>G
c.4427C>G
c.4059C>G (p.Asp1353Glu)
c.3336C>G (p.Asp1112Glu)
c.330C>G (p.Asp110Glu)
n.3797C>G
c.2874C>G (p.Asp958Glu)
n.4654C>G
n.4637C>G
dbSNP
12g.45852629C>TCA6526675ARID2c.4506C>T (p.Asp1502=)
c.715C>T
c.4427C>T
c.4059C>T (p.Asp1353=)
c.3336C>T (p.Asp1112=)
c.330C>T (p.Asp110=)
n.3797C>T
c.2874C>T (p.Asp958=)
n.4654C>T
n.4637C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852630G>ACA6526676ARID2c.4507G>A (p.Val1503Ile)
c.716G>A
c.4428G>A
c.4060G>A (p.Val1354Ile)
c.3337G>A (p.Val1113Ile)
c.331G>A (p.Val111Ile)
n.3798G>A
c.2875G>A (p.Val959Ile)
n.4655G>A
n.4638G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.45852630G>CCA6526677ARID2c.4507G>C (p.Val1503Leu)
c.716G>C
c.4428G>C
c.4060G>C (p.Val1354Leu)
c.3337G>C (p.Val1113Leu)
c.331G>C (p.Val111Leu)
n.3798G>C
c.2875G>C (p.Val959Leu)
n.4655G>C
n.4638G>C
dbSNP ExAC gnomAD v2
12g.45852630G=CA2033475709ARID2c.4507G= (p.Val1503=)
c.716G=
c.4428G=
c.4060G= (p.Val1354=)
c.3337G= (p.Val1113=)
c.331G= (p.Val111=)
n.3798G=
c.2875G= (p.Val959=)
n.4655G=
n.4638G=
12g.45852630G>TCA384491872ARID2c.4507G>T (p.Val1503Phe)
c.716G>T
c.4428G>T
c.4060G>T (p.Val1354Phe)
c.3337G>T (p.Val1113Phe)
c.331G>T (p.Val111Phe)
n.3798G>T
c.2875G>T (p.Val959Phe)
n.4655G>T
n.4638G>T
dbSNP
12g.45852631T>ACA384491874ARID2c.4508T>A (p.Val1503Asp)
c.717T>A
c.4429T>A
c.4061T>A (p.Val1354Asp)
c.3338T>A (p.Val1113Asp)
c.332T>A (p.Val111Asp)
n.3799T>A
c.2876T>A (p.Val959Asp)
n.4656T>A
n.4639T>A
12g.45852631T>CCA384491873ARID2c.4508T>C (p.Val1503Ala)
c.717T>C
c.4429T>C
c.4061T>C (p.Val1354Ala)
c.3338T>C (p.Val1113Ala)
c.332T>C (p.Val111Ala)
n.3799T>C
c.2876T>C (p.Val959Ala)
n.4656T>C
n.4639T>C
12g.45852631T>GCA384491875ARID2c.4508T>G (p.Val1503Gly)
c.717T>G
c.4429T>G
c.4061T>G (p.Val1354Gly)
c.3338T>G (p.Val1113Gly)
c.332T>G (p.Val111Gly)
n.3799T>G
c.2876T>G (p.Val959Gly)
n.4656T>G
n.4639T>G
dbSNP gnomAD v3 gnomAD v4
12g.45852631T=CA2033475710ARID2c.4508T= (p.Val1503=)
c.717T=
c.4429T=
c.4061T= (p.Val1354=)
c.3338T= (p.Val1113=)
c.332T= (p.Val111=)
n.3799T=
c.2876T= (p.Val959=)
n.4656T=
n.4639T=
12g.45852632delCA479693872ARID2c.4509del (p.Arg1504GlyfsTer12)
c.718del
c.4430del
c.4062del (p.Arg1355GlyfsTer12)
c.3339del (p.Arg1114GlyfsTer12)
c.333del (p.Arg112GlyfsTer12)
n.3800del
c.2877del (p.Arg960GlyfsTer12)
n.4657del
n.4640del
COSMIC
12g.45852631_45852632insACA2741808815ARID2c.4508_4509insA (p.Arg1504SerfsTer20)
c.717_718insA
c.4429_4430insA
c.4061_4062insA (p.Arg1355SerfsTer20)
c.3338_3339insA (p.Arg1114SerfsTer20)
c.332_333insA (p.Arg112SerfsTer20)
n.3799_3800insA
c.2876_2877insA (p.Arg960SerfsTer20)
n.4656_4657insA
n.4639_4640insA
12g.45852632T>ACA479693873ARID2c.4509T>A (p.Val1503=)
c.718T>A
c.4430T>A
c.4062T>A (p.Val1354=)
c.3339T>A (p.Val1113=)
c.333T>A (p.Val111=)
n.3800T>A
c.2877T>A (p.Val959=)
n.4657T>A
n.4640T>A
dbSNP
12g.45852632T>CCA479693874ARID2c.4509T>C (p.Val1503=)
c.718T>C
c.4430T>C
c.4062T>C (p.Val1354=)
c.3339T>C (p.Val1113=)
c.333T>C (p.Val111=)
n.3800T>C
c.2877T>C (p.Val959=)
n.4657T>C
n.4640T>C
dbSNP
12g.45852632T>GCA479693875ARID2c.4509T>G (p.Val1503=)
c.718T>G
c.4430T>G
c.4062T>G (p.Val1354=)
c.3339T>G (p.Val1113=)
c.333T>G (p.Val111=)
n.3800T>G
c.2877T>G (p.Val959=)
n.4657T>G
n.4640T>G
COSMIC
12g.45852633C>ACA6526678ARID2c.4510C>A (p.Arg1504=)
c.719C>A
c.4431C>A
c.4063C>A (p.Arg1355=)
c.3340C>A (p.Arg1114=)
c.334C>A (p.Arg112=)
n.3801C>A
c.2878C>A (p.Arg960=)
n.4658C>A
n.4641C>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852633C=CA2033475711ARID2c.4510C= (p.Arg1504=)
c.719C=
c.4431C=
c.4063C= (p.Arg1355=)
c.3340C= (p.Arg1114=)
c.334C= (p.Arg112=)
n.3801C=
c.2878C= (p.Arg960=)
n.4658C=
n.4641C=
12g.45852633C>GCA384491876ARID2c.4510C>G (p.Arg1504Gly)
c.719C>G
c.4431C>G
c.4063C>G (p.Arg1355Gly)
c.3340C>G (p.Arg1114Gly)
c.334C>G (p.Arg112Gly)
n.3801C>G
c.2878C>G (p.Arg960Gly)
n.4658C>G
n.4641C>G
dbSNP
12g.45852633C>TCA156958ARID2c.4510C>T (p.Arg1504Trp)
c.719C>T
c.4431C>T
c.4063C>T (p.Arg1355Trp)
c.3340C>T (p.Arg1114Trp)
c.334C>T (p.Arg112Trp)
n.3801C>T
c.2878C>T (p.Arg960Trp)
n.4658C>T
n.4641C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.45852634G>ACA6526679ARID2c.4511G>A (p.Arg1504Gln)
c.720G>A
c.4432G>A
c.4064G>A (p.Arg1355Gln)
c.3341G>A (p.Arg1114Gln)
c.335G>A (p.Arg112Gln)
n.3802G>A
c.2879G>A (p.Arg960Gln)
n.4659G>A
n.4642G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.45852634G>CCA384491877ARID2c.4511G>C (p.Arg1504Pro)
c.720G>C
c.4432G>C
c.4064G>C (p.Arg1355Pro)
c.3341G>C (p.Arg1114Pro)
c.335G>C (p.Arg112Pro)
n.3802G>C
c.2879G>C (p.Arg960Pro)
n.4659G>C
n.4642G>C
dbSNP
12g.45852634G=CA2033475712ARID2c.4511G= (p.Arg1504=)
c.720G=
c.4432G=
c.4064G= (p.Arg1355=)
c.3341G= (p.Arg1114=)
c.335G= (p.Arg112=)
n.3802G=
c.2879G= (p.Arg960=)
n.4659G=
n.4642G=
12g.45852634G>TCA384491878ARID2c.4511G>T (p.Arg1504Leu)
c.720G>T
c.4432G>T
c.4064G>T (p.Arg1355Leu)
c.3341G>T (p.Arg1114Leu)
c.335G>T (p.Arg112Leu)
n.3802G>T
c.2879G>T (p.Arg960Leu)
n.4659G>T
n.4642G>T
dbSNP
12g.45852635G>ACA6526680ARID2c.4512G>A (p.Arg1504=)
c.721G>A
c.4433G>A
c.4065G>A (p.Arg1355=)
c.3342G>A (p.Arg1114=)
c.336G>A (p.Arg112=)
n.3803G>A
c.2880G>A (p.Arg960=)
n.4660G>A
n.4643G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.45852635G>CCA479693876ARID2c.4512G>C (p.Arg1504=)
c.721G>C
c.4433G>C
c.4065G>C (p.Arg1355=)
c.3342G>C (p.Arg1114=)
c.336G>C (p.Arg112=)
n.3803G>C
c.2880G>C (p.Arg960=)
n.4660G>C
n.4643G>C
dbSNP
12g.45852635G=CA2033475713ARID2c.4512G= (p.Arg1504=)
c.721G=
c.4433G=
c.4065G= (p.Arg1355=)
c.3342G= (p.Arg1114=)
c.336G= (p.Arg112=)
n.3803G=
c.2880G= (p.Arg960=)
n.4660G=
n.4643G=
12g.45852635G>TCA479693877ARID2c.4512G>T (p.Arg1504=)
c.721G>T
c.4433G>T
c.4065G>T (p.Arg1355=)
c.3342G>T (p.Arg1114=)
c.336G>T (p.Arg112=)
n.3803G>T
c.2880G>T (p.Arg960=)
n.4660G>T
n.4643G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.45852636T>ACA384491881ARID2c.4513T>A (p.Ser1505Thr)
c.722T>A
c.4434T>A
c.4066T>A (p.Ser1356Thr)
c.3343T>A (p.Ser1115Thr)
c.337T>A (p.Ser113Thr)
n.3804T>A
c.2881T>A (p.Ser961Thr)
n.4661T>A
n.4644T>A
12g.45852636T>CCA384491879ARID2c.4513T>C (p.Ser1505Pro)
c.722T>C
c.4434T>C
c.4066T>C (p.Ser1356Pro)
c.3343T>C (p.Ser1115Pro)
c.337T>C (p.Ser113Pro)
n.3804T>C
c.2881T>C (p.Ser961Pro)
n.4661T>C
n.4644T>C
12g.45852636T>GCA384491880ARID2c.4513T>G (p.Ser1505Ala)
c.722T>G
c.4434T>G
c.4066T>G (p.Ser1356Ala)
c.3343T>G (p.Ser1115Ala)
c.337T>G (p.Ser113Ala)
n.3804T>G
c.2881T>G (p.Ser961Ala)
n.4661T>G
n.4644T>G
12g.45852637C>ACA384491882ARID2c.4514C>A (p.Ser1505Tyr)
c.723C>A
c.4435C>A
c.4067C>A (p.Ser1356Tyr)
c.3344C>A (p.Ser1115Tyr)
c.338C>A (p.Ser113Tyr)
n.3805C>A
c.2882C>A (p.Ser961Tyr)
n.4662C>A
n.4645C>A
12g.45852637C>GCA384491883ARID2c.4514C>G (p.Ser1505Cys)
c.723C>G
c.4435C>G
c.4067C>G (p.Ser1356Cys)
c.3344C>G (p.Ser1115Cys)
c.338C>G (p.Ser113Cys)
n.3805C>G
c.2882C>G (p.Ser961Cys)
n.4662C>G
n.4645C>G
dbSNP
12g.45852637C>TCA384491884ARID2c.4514C>T (p.Ser1505Phe)
c.723C>T
c.4435C>T
c.4067C>T (p.Ser1356Phe)
c.3344C>T (p.Ser1115Phe)
c.338C>T (p.Ser113Phe)
n.3805C>T
c.2882C>T (p.Ser961Phe)
n.4662C>T
n.4645C>T
dbSNP
12g.45852638T>ACA479693878ARID2c.4515T>A (p.Ser1505=)
c.724T>A
c.4436T>A
c.4068T>A (p.Ser1356=)
c.3345T>A (p.Ser1115=)
c.339T>A (p.Ser113=)
n.3806T>A
c.2883T>A (p.Ser961=)
n.4663T>A
n.4646T>A
dbSNP
12g.45852638T>CCA479693879ARID2c.4515T>C (p.Ser1505=)
c.724T>C
c.4436T>C
c.4068T>C (p.Ser1356=)
c.3345T>C (p.Ser1115=)
c.339T>C (p.Ser113=)
n.3806T>C
c.2883T>C (p.Ser961=)
n.4663T>C
n.4646T>C
dbSNP
12g.45852638T>GCA479693880ARID2c.4515T>G (p.Ser1505=)
c.724T>G
c.4436T>G
c.4068T>G (p.Ser1356=)
c.3345T>G (p.Ser1115=)
c.339T>G (p.Ser113=)
n.3806T>G
c.2883T>G (p.Ser961=)
n.4663T>G
n.4646T>G
12g.45852639A>CCA384491885ARID2c.4516A>C (p.Thr1506Pro)
c.725A>C
c.4437A>C
c.4069A>C (p.Thr1357Pro)
c.3346A>C (p.Thr1116Pro)
c.340A>C (p.Thr114Pro)
n.3807A>C
c.2884A>C (p.Thr962Pro)
n.4664A>C
n.4647A>C
dbSNP
12g.45852639A>GCA384491886ARID2c.4516A>G (p.Thr1506Ala)
c.725A>G
c.4437A>G
c.4069A>G (p.Thr1357Ala)
c.3346A>G (p.Thr1116Ala)
c.340A>G (p.Thr114Ala)
n.3807A>G
c.2884A>G (p.Thr962Ala)
n.4664A>G
n.4647A>G
dbSNP gnomAD v4
12g.45852639A>TCA384491887ARID2c.4516A>T (p.Thr1506Ser)
c.725A>T
c.4437A>T
c.4069A>T (p.Thr1357Ser)
c.3346A>T (p.Thr1116Ser)
c.340A>T (p.Thr114Ser)
n.3807A>T
c.2884A>T (p.Thr962Ser)
n.4664A>T
n.4647A>T
dbSNP

Number of alleles fetched