| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.45852693A= | CA2033475734 | ARID2 | c.4570A= (p.Arg1524=) c.779A= c.4491A= c.4123A= (p.Arg1375=) c.3400A= (p.Arg1134=) c.394A= (p.Arg132=) n.3861A= c.2938A= (p.Arg980=) n.4718A= n.4701A= | |
| 12 | g.45852693A>C | CA479694098 | ARID2 | c.4570A>C (p.Arg1524=) c.779A>C c.4491A>C c.4123A>C (p.Arg1375=) c.3400A>C (p.Arg1134=) c.394A>C (p.Arg132=) n.3861A>C c.2938A>C (p.Arg980=) n.4718A>C n.4701A>C | |
| 12 | g.45852693A>G | CA384492002 | ARID2 | c.4570A>G (p.Arg1524Gly) c.779A>G c.4491A>G c.4123A>G (p.Arg1375Gly) c.3400A>G (p.Arg1134Gly) c.394A>G (p.Arg132Gly) n.3861A>G c.2938A>G (p.Arg980Gly) n.4718A>G n.4701A>G | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852693A>T | CA384492003 | ARID2 | c.4570A>T (p.Arg1524Trp) c.779A>T c.4491A>T c.4123A>T (p.Arg1375Trp) c.3400A>T (p.Arg1134Trp) c.394A>T (p.Arg132Trp) n.3861A>T c.2938A>T (p.Arg980Trp) n.4718A>T n.4701A>T | dbSNP |
| 12 | g.45852694G>A | CA384492004 | ARID2 | c.4571G>A (p.Arg1524Lys) c.780G>A c.4492G>A c.4124G>A (p.Arg1375Lys) c.3401G>A (p.Arg1134Lys) c.395G>A (p.Arg132Lys) n.3862G>A c.2939G>A (p.Arg980Lys) n.4719G>A n.4702G>A | |
| 12 | g.45852694G>C | CA6526689 | ARID2 | c.4571G>C (p.Arg1524Thr) c.780G>C c.4492G>C c.4124G>C (p.Arg1375Thr) c.3401G>C (p.Arg1134Thr) c.395G>C (p.Arg132Thr) n.3862G>C c.2939G>C (p.Arg980Thr) n.4719G>C n.4702G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852694G= | CA2033475735 | ARID2 | c.4571G= (p.Arg1524=) c.780G= c.4492G= c.4124G= (p.Arg1375=) c.3401G= (p.Arg1134=) c.395G= (p.Arg132=) n.3862G= c.2939G= (p.Arg980=) n.4719G= n.4702G= | |
| 12 | g.45852694G>T | CA384492005 | ARID2 | c.4571G>T (p.Arg1524Met) c.780G>T c.4492G>T c.4124G>T (p.Arg1375Met) c.3401G>T (p.Arg1134Met) c.395G>T (p.Arg132Met) n.3862G>T c.2939G>T (p.Arg980Met) n.4719G>T n.4702G>T | |
| 12 | g.45852695G>A | CA479694099 | ARID2 | c.4572G>A (p.Arg1524=) c.781G>A c.4493G>A c.4125G>A (p.Arg1375=) c.3402G>A (p.Arg1134=) c.396G>A (p.Arg132=) n.3863G>A c.2940G>A (p.Arg980=) n.4720G>A n.4703G>A | |
| 12 | g.45852695G>C | CA384492006 | ARID2 | c.4572G>C (p.Arg1524Ser) c.781G>C c.4493G>C c.4125G>C (p.Arg1375Ser) c.3402G>C (p.Arg1134Ser) c.396G>C (p.Arg132Ser) n.3863G>C c.2940G>C (p.Arg980Ser) n.4720G>C n.4703G>C | |
| 12 | g.45852695G>T | CA384492007 | ARID2 | c.4572G>T (p.Arg1524Ser) c.781G>T c.4493G>T c.4125G>T (p.Arg1375Ser) c.3402G>T (p.Arg1134Ser) c.396G>T (p.Arg132Ser) n.3863G>T c.2940G>T (p.Arg980Ser) n.4720G>T n.4703G>T | |
| 12 | g.45852696G>A | CA384492008 | ARID2 | c.4573G>A (p.Glu1525Lys) c.782G>A c.4494G>A c.4126G>A (p.Glu1376Lys) c.3403G>A (p.Glu1135Lys) c.397G>A (p.Glu133Lys) n.3864G>A c.2941G>A (p.Glu981Lys) n.4721G>A n.4704G>A | |
| 12 | g.45852696G>C | CA384492009 | ARID2 | c.4573G>C (p.Glu1525Gln) c.782G>C c.4494G>C c.4126G>C (p.Glu1376Gln) c.3403G>C (p.Glu1135Gln) c.397G>C (p.Glu133Gln) n.3864G>C c.2941G>C (p.Glu981Gln) n.4721G>C n.4704G>C | dbSNP |
| 12 | g.45852696G>T | CA384492010 | ARID2 | c.4573G>T (p.Glu1525Ter) c.782G>T c.4494G>T c.4126G>T (p.Glu1376Ter) c.3403G>T (p.Glu1135Ter) c.397G>T (p.Glu133Ter) n.3864G>T c.2941G>T (p.Glu981Ter) n.4721G>T n.4704G>T | |
| 12 | g.45852697A= | CA2033475736 | ARID2 | c.4574A= (p.Glu1525=) c.783A= c.4495A= c.4127A= (p.Glu1376=) c.3404A= (p.Glu1135=) c.398A= (p.Glu133=) n.3865A= c.2942A= (p.Glu981=) n.4722A= n.4705A= | |
| 12 | g.45852697A>C | CA384492011 | ARID2 | c.4574A>C (p.Glu1525Ala) c.783A>C c.4495A>C c.4127A>C (p.Glu1376Ala) c.3404A>C (p.Glu1135Ala) c.398A>C (p.Glu133Ala) n.3865A>C c.2942A>C (p.Glu981Ala) n.4722A>C n.4705A>C | |
| 12 | g.45852697A>G | CA384492012 | ARID2 | c.4574A>G (p.Glu1525Gly) c.783A>G c.4495A>G c.4127A>G (p.Glu1376Gly) c.3404A>G (p.Glu1135Gly) c.398A>G (p.Glu133Gly) n.3865A>G c.2942A>G (p.Glu981Gly) n.4722A>G n.4705A>G | dbSNP |
| 12 | g.45852697A>T | CA384492013 | ARID2 | c.4574A>T (p.Glu1525Val) c.783A>T c.4495A>T c.4127A>T (p.Glu1376Val) c.3404A>T (p.Glu1135Val) c.398A>T (p.Glu133Val) n.3865A>T c.2942A>T (p.Glu981Val) n.4722A>T n.4705A>T | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852699del | CA479694100 | ARID2 | c.4576del (p.Thr1526GlnfsTer9) c.785del c.4497del c.4129del (p.Thr1377GlnfsTer9) c.3406del (p.Thr1136GlnfsTer9) c.400del (p.Thr134GlnfsTer9) n.3867del c.2944del (p.Thr982GlnfsTer9) n.4724del n.4707del | COSMIC COSMIC |
| 12 | g.45852698A>C | CA384492014 | ARID2 | c.4575A>C (p.Glu1525Asp) c.784A>C c.4496A>C c.4128A>C (p.Glu1376Asp) c.3405A>C (p.Glu1135Asp) c.399A>C (p.Glu133Asp) n.3866A>C c.2943A>C (p.Glu981Asp) n.4723A>C n.4706A>C | dbSNP |
| 12 | g.45852698A>G | CA479694101 | ARID2 | c.4575A>G (p.Glu1525=) c.784A>G c.4496A>G c.4128A>G (p.Glu1376=) c.3405A>G (p.Glu1135=) c.399A>G (p.Glu133=) n.3866A>G c.2943A>G (p.Glu981=) n.4723A>G n.4706A>G | dbSNP |
| 12 | g.45852698A>T | CA384492015 | ARID2 | c.4575A>T (p.Glu1525Asp) c.784A>T c.4496A>T c.4128A>T (p.Glu1376Asp) c.3405A>T (p.Glu1135Asp) c.399A>T (p.Glu133Asp) n.3866A>T c.2943A>T (p.Glu981Asp) n.4723A>T n.4706A>T | dbSNP |
| 12 | g.45852699A= | CA2033475737 | ARID2 | c.4576A= (p.Thr1526=) c.785A= c.4497A= c.4129A= (p.Thr1377=) c.3406A= (p.Thr1136=) c.400A= (p.Thr134=) n.3867A= c.2944A= (p.Thr982=) n.4724A= n.4707A= | |
| 12 | g.45852699A>C | CA384492016 | ARID2 | c.4576A>C (p.Thr1526Pro) c.785A>C c.4497A>C c.4129A>C (p.Thr1377Pro) c.3406A>C (p.Thr1136Pro) c.400A>C (p.Thr134Pro) n.3867A>C c.2944A>C (p.Thr982Pro) n.4724A>C n.4707A>C | dbSNP |
| 12 | g.45852699A>G | CA236400859 | ARID2 | c.4576A>G (p.Thr1526Ala) c.785A>G c.4497A>G c.4129A>G (p.Thr1377Ala) c.3406A>G (p.Thr1136Ala) c.400A>G (p.Thr134Ala) n.3867A>G c.2944A>G (p.Thr982Ala) n.4724A>G n.4707A>G | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852699A>T | CA384492017 | ARID2 | c.4576A>T (p.Thr1526Ser) c.785A>T c.4497A>T c.4129A>T (p.Thr1377Ser) c.3406A>T (p.Thr1136Ser) c.400A>T (p.Thr134Ser) n.3867A>T c.2944A>T (p.Thr982Ser) n.4724A>T n.4707A>T | dbSNP |
| 12 | g.45852700C>A | CA384492018 | ARID2 | c.4577C>A (p.Thr1526Lys) c.786C>A c.4498C>A c.4130C>A (p.Thr1377Lys) c.3407C>A (p.Thr1136Lys) c.401C>A (p.Thr134Lys) n.3868C>A c.2945C>A (p.Thr982Lys) n.4725C>A n.4708C>A | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852700C= | CA2033475738 | ARID2 | c.4577C= (p.Thr1526=) c.786C= c.4498C= c.4130C= (p.Thr1377=) c.3407C= (p.Thr1136=) c.401C= (p.Thr134=) n.3868C= c.2945C= (p.Thr982=) n.4725C= n.4708C= | |
| 12 | g.45852700C>G | CA384492019 | ARID2 | c.4577C>G (p.Thr1526Arg) c.786C>G c.4498C>G c.4130C>G (p.Thr1377Arg) c.3407C>G (p.Thr1136Arg) c.401C>G (p.Thr134Arg) n.3868C>G c.2945C>G (p.Thr982Arg) n.4725C>G n.4708C>G | dbSNP |
| 12 | g.45852700C>T | CA236400862 | ARID2 | c.4577C>T (p.Thr1526Ile) c.786C>T c.4498C>T c.4130C>T (p.Thr1377Ile) c.3407C>T (p.Thr1136Ile) c.401C>T (p.Thr134Ile) n.3868C>T c.2945C>T (p.Thr982Ile) n.4725C>T n.4708C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852701A>C | CA479694102 | ARID2 | c.4578A>C (p.Thr1526=) c.787A>C c.4499A>C c.4131A>C (p.Thr1377=) c.3408A>C (p.Thr1136=) c.402A>C (p.Thr134=) n.3869A>C c.2946A>C (p.Thr982=) n.4726A>C n.4709A>C | |
| 12 | g.45852701A>G | CA479694103 | ARID2 | c.4578A>G (p.Thr1526=) c.787A>G c.4499A>G c.4131A>G (p.Thr1377=) c.3408A>G (p.Thr1136=) c.402A>G (p.Thr134=) n.3869A>G c.2946A>G (p.Thr982=) n.4726A>G n.4709A>G | |
| 12 | g.45852701A>T | CA479694104 | ARID2 | c.4578A>T (p.Thr1526=) c.787A>T c.4499A>T c.4131A>T (p.Thr1377=) c.3408A>T (p.Thr1136=) c.402A>T (p.Thr134=) n.3869A>T c.2946A>T (p.Thr982=) n.4726A>T n.4709A>T | dbSNP |
| 12 | g.45852702G>A | CA384492020 | ARID2 | c.4579G>A (p.Val1527Ile) c.788G>A c.4500G>A c.4132G>A (p.Val1378Ile) c.3409G>A (p.Val1137Ile) c.403G>A (p.Val135Ile) n.3870G>A c.2947G>A (p.Val983Ile) n.4727G>A n.4710G>A | dbSNP |
| 12 | g.45852702G>C | CA384492021 | ARID2 | c.4579G>C (p.Val1527Leu) c.788G>C c.4500G>C c.4132G>C (p.Val1378Leu) c.3409G>C (p.Val1137Leu) c.403G>C (p.Val135Leu) n.3870G>C c.2947G>C (p.Val983Leu) n.4727G>C n.4710G>C | dbSNP |
| 12 | g.45852702G>T | CA384492022 | ARID2 | c.4579G>T (p.Val1527Phe) c.788G>T c.4500G>T c.4132G>T (p.Val1378Phe) c.3409G>T (p.Val1137Phe) c.403G>T (p.Val135Phe) n.3870G>T c.2947G>T (p.Val983Phe) n.4727G>T n.4710G>T | |
| 12 | g.45852703T>A | CA384492023 | ARID2 | c.4580T>A (p.Val1527Asp) c.789T>A c.4501T>A c.4133T>A (p.Val1378Asp) c.3410T>A (p.Val1137Asp) c.404T>A (p.Val135Asp) n.3871T>A c.2948T>A (p.Val983Asp) n.4728T>A n.4711T>A | dbSNP |
| 12 | g.45852703T>C | CA384492024 | ARID2 | c.4580T>C (p.Val1527Ala) c.789T>C c.4501T>C c.4133T>C (p.Val1378Ala) c.3410T>C (p.Val1137Ala) c.404T>C (p.Val135Ala) n.3871T>C c.2948T>C (p.Val983Ala) n.4728T>C n.4711T>C | dbSNP gnomAD v2 |
| 12 | g.45852703T>G | CA384492025 | ARID2 | c.4580T>G (p.Val1527Gly) c.789T>G c.4501T>G c.4133T>G (p.Val1378Gly) c.3410T>G (p.Val1137Gly) c.404T>G (p.Val135Gly) n.3871T>G c.2948T>G (p.Val983Gly) n.4728T>G n.4711T>G | dbSNP |
| 12 | g.45852703T= | CA2033475739 | ARID2 | c.4580T= (p.Val1527=) c.789T= c.4501T= c.4133T= (p.Val1378=) c.3410T= (p.Val1137=) c.404T= (p.Val135=) n.3871T= c.2948T= (p.Val983=) n.4728T= n.4711T= | |
| 12 | g.45852704C>A | CA479694105 | ARID2 | c.4581C>A (p.Val1527=) c.790C>A c.4502C>A c.4134C>A (p.Val1378=) c.3411C>A (p.Val1137=) c.405C>A (p.Val135=) n.3872C>A c.2949C>A (p.Val983=) n.4729C>A n.4712C>A | dbSNP gnomAD v4 |
| 12 | g.45852704C= | CA2033475740 | ARID2 | c.4581C= (p.Val1527=) c.790C= c.4502C= c.4134C= (p.Val1378=) c.3411C= (p.Val1137=) c.405C= (p.Val135=) n.3872C= c.2949C= (p.Val983=) n.4729C= n.4712C= | |
| 12 | g.45852704C>G | CA6526690 | ARID2 | c.4581C>G (p.Val1527=) c.790C>G c.4502C>G c.4134C>G (p.Val1378=) c.3411C>G (p.Val1137=) c.405C>G (p.Val135=) n.3872C>G c.2949C>G (p.Val983=) n.4729C>G n.4712C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852704C>T | CA6526691 | ARID2 | c.4581C>T (p.Val1527=) c.790C>T c.4502C>T c.4134C>T (p.Val1378=) c.3411C>T (p.Val1137=) c.405C>T (p.Val135=) n.3872C>T c.2949C>T (p.Val983=) n.4729C>T n.4712C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852705G>A | CA6526692 | ARID2 | c.4582G>A (p.Ala1528Thr) c.791G>A c.4503G>A c.4135G>A (p.Ala1379Thr) c.3412G>A (p.Ala1138Thr) c.406G>A (p.Ala136Thr) n.3873G>A c.2950G>A (p.Ala984Thr) n.4730G>A n.4713G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 12 | g.45852705G>C | CA384492026 | ARID2 | c.4582G>C (p.Ala1528Pro) c.791G>C c.4503G>C c.4135G>C (p.Ala1379Pro) c.3412G>C (p.Ala1138Pro) c.406G>C (p.Ala136Pro) n.3873G>C c.2950G>C (p.Ala984Pro) n.4730G>C n.4713G>C | dbSNP |
| 12 | g.45852705G= | CA2033475741 | ARID2 | c.4582G= (p.Ala1528=) c.791G= c.4503G= c.4135G= (p.Ala1379=) c.3412G= (p.Ala1138=) c.406G= (p.Ala136=) n.3873G= c.2950G= (p.Ala984=) n.4730G= n.4713G= | |
| 12 | g.45852705G>T | CA384492027 | ARID2 | c.4582G>T (p.Ala1528Ser) c.791G>T c.4503G>T c.4135G>T (p.Ala1379Ser) c.3412G>T (p.Ala1138Ser) c.406G>T (p.Ala136Ser) n.3873G>T c.2950G>T (p.Ala984Ser) n.4730G>T n.4713G>T | dbSNP |
| 12 | g.45852706C>A | CA384492028 | ARID2 | c.4583C>A (p.Ala1528Glu) c.792C>A c.4504C>A c.4136C>A (p.Ala1379Glu) c.3413C>A (p.Ala1138Glu) c.407C>A (p.Ala136Glu) n.3874C>A c.2951C>A (p.Ala984Glu) n.4731C>A n.4714C>A | dbSNP |
| 12 | g.45852706C>G | CA384492029 | ARID2 | c.4583C>G (p.Ala1528Gly) c.792C>G c.4504C>G c.4136C>G (p.Ala1379Gly) c.3413C>G (p.Ala1138Gly) c.407C>G (p.Ala136Gly) n.3874C>G c.2951C>G (p.Ala984Gly) n.4731C>G n.4714C>G | dbSNP |
| 12 | g.45852706C>T | CA384492030 | ARID2 | c.4583C>T (p.Ala1528Val) c.792C>T c.4504C>T c.4136C>T (p.Ala1379Val) c.3413C>T (p.Ala1138Val) c.407C>T (p.Ala136Val) n.3874C>T c.2951C>T (p.Ala984Val) n.4731C>T n.4714C>T | dbSNP COSMIC |
| 12 | g.45852707A= | CA2033475742 | ARID2 | c.4584A= (p.Ala1528=) c.793A= c.4505A= c.4137A= (p.Ala1379=) c.3414A= (p.Ala1138=) c.408A= (p.Ala136=) n.3875A= c.2952A= (p.Ala984=) n.4732A= n.4715A= | |
| 12 | g.45852707A>C | CA479694106 | ARID2 | c.4584A>C (p.Ala1528=) c.793A>C c.4505A>C c.4137A>C (p.Ala1379=) c.3414A>C (p.Ala1138=) c.408A>C (p.Ala136=) n.3875A>C c.2952A>C (p.Ala984=) n.4732A>C n.4715A>C | dbSNP |
| 12 | g.45852707A>G | CA479694107 | ARID2 | c.4584A>G (p.Ala1528=) c.793A>G c.4505A>G c.4137A>G (p.Ala1379=) c.3414A>G (p.Ala1138=) c.408A>G (p.Ala136=) n.3875A>G c.2952A>G (p.Ala984=) n.4732A>G n.4715A>G | dbSNP |
| 12 | g.45852707A>T | CA6526693 | ARID2 | c.4584A>T (p.Ala1528=) c.793A>T c.4505A>T c.4137A>T (p.Ala1379=) c.3414A>T (p.Ala1138=) c.408A>T (p.Ala136=) n.3875A>T c.2952A>T (p.Ala984=) n.4732A>T n.4715A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.45852708G>A | CA6526694 | ARID2 | c.4585G>A (p.Gly1529Arg) c.794G>A c.4506G>A c.4138G>A (p.Gly1380Arg) c.3415G>A (p.Gly1139Arg) c.409G>A (p.Gly137Arg) n.3876G>A c.2953G>A (p.Gly985Arg) n.4733G>A n.4716G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852708G>C | CA384492031 | ARID2 | c.4585G>C (p.Gly1529Arg) c.794G>C c.4506G>C c.4138G>C (p.Gly1380Arg) c.3415G>C (p.Gly1139Arg) c.409G>C (p.Gly137Arg) n.3876G>C c.2953G>C (p.Gly985Arg) n.4733G>C n.4716G>C | dbSNP |
| 12 | g.45852708G= | CA2033475743 | ARID2 | c.4585G= (p.Gly1529=) c.794G= c.4506G= c.4138G= (p.Gly1380=) c.3415G= (p.Gly1139=) c.409G= (p.Gly137=) n.3876G= c.2953G= (p.Gly985=) n.4733G= n.4716G= | |
| 12 | g.45852708G>T | CA384492032 | ARID2 | c.4585G>T (p.Gly1529Ter) c.794G>T c.4506G>T c.4138G>T (p.Gly1380Ter) c.3415G>T (p.Gly1139Ter) c.409G>T (p.Gly137Ter) n.3876G>T c.2953G>T (p.Gly985Ter) n.4733G>T n.4716G>T | dbSNP COSMIC |
| 12 | g.45852709G>A | CA384492033 | ARID2 | c.4586G>A (p.Gly1529Glu) c.795G>A c.4507G>A c.4139G>A (p.Gly1380Glu) c.3416G>A (p.Gly1139Glu) c.410G>A (p.Gly137Glu) n.3877G>A c.2954G>A (p.Gly985Glu) n.4734G>A n.4717G>A | dbSNP |
| 12 | g.45852709G>C | CA384492034 | ARID2 | c.4586G>C (p.Gly1529Ala) c.795G>C c.4507G>C c.4139G>C (p.Gly1380Ala) c.3416G>C (p.Gly1139Ala) c.410G>C (p.Gly137Ala) n.3877G>C c.2954G>C (p.Gly985Ala) n.4734G>C n.4717G>C | dbSNP |
| 12 | g.45852709G>T | CA384492035 | ARID2 | c.4586G>T (p.Gly1529Val) c.795G>T c.4507G>T c.4139G>T (p.Gly1380Val) c.3416G>T (p.Gly1139Val) c.410G>T (p.Gly137Val) n.3877G>T c.2954G>T (p.Gly985Val) n.4734G>T n.4717G>T | dbSNP |
| 12 | g.45852710A>C | CA479694108 | ARID2 | c.4587A>C (p.Gly1529=) c.796A>C c.4508A>C c.4140A>C (p.Gly1380=) c.3417A>C (p.Gly1139=) c.411A>C (p.Gly137=) n.3878A>C c.2955A>C (p.Gly985=) n.4735A>C n.4718A>C | |
| 12 | g.45852710A>G | CA479694109 | ARID2 | c.4587A>G (p.Gly1529=) c.796A>G c.4508A>G c.4140A>G (p.Gly1380=) c.3417A>G (p.Gly1139=) c.411A>G (p.Gly137=) n.3878A>G c.2955A>G (p.Gly985=) n.4735A>G n.4718A>G | dbSNP |
| 12 | g.45852710A>T | CA479694110 | ARID2 | c.4587A>T (p.Gly1529=) c.796A>T c.4508A>T c.4140A>T (p.Gly1380=) c.3417A>T (p.Gly1139=) c.411A>T (p.Gly137=) n.3878A>T c.2955A>T (p.Gly985=) n.4735A>T n.4718A>T | |
| 12 | g.45852711A>C | CA384492036 | ARID2 | c.4588A>C (p.Ile1530Leu) c.797A>C c.4509A>C c.4141A>C (p.Ile1381Leu) c.3418A>C (p.Ile1140Leu) c.412A>C (p.Ile138Leu) n.3879A>C c.2956A>C (p.Ile986Leu) n.4736A>C n.4719A>C | |
| 12 | g.45852711A>G | CA384492037 | ARID2 | c.4588A>G (p.Ile1530Val) c.797A>G c.4509A>G c.4141A>G (p.Ile1381Val) c.3418A>G (p.Ile1140Val) c.412A>G (p.Ile138Val) n.3879A>G c.2956A>G (p.Ile986Val) n.4736A>G n.4719A>G | gnomAD v4 |
| 12 | g.45852711A>T | CA384492038 | ARID2 | c.4588A>T (p.Ile1530Phe) c.797A>T c.4509A>T c.4141A>T (p.Ile1381Phe) c.3418A>T (p.Ile1140Phe) c.412A>T (p.Ile138Phe) n.3879A>T c.2956A>T (p.Ile986Phe) n.4736A>T n.4719A>T | dbSNP |
| 12 | g.45852712T>A | CA384492039 | ARID2 | c.4589T>A (p.Ile1530Asn) c.798T>A c.4510T>A c.4142T>A (p.Ile1381Asn) c.3419T>A (p.Ile1140Asn) c.413T>A (p.Ile138Asn) n.3880T>A c.2957T>A (p.Ile986Asn) n.4737T>A n.4720T>A | |
| 12 | g.45852712T>C | CA384492040 | ARID2 | c.4589T>C (p.Ile1530Thr) c.798T>C c.4510T>C c.4142T>C (p.Ile1381Thr) c.3419T>C (p.Ile1140Thr) c.413T>C (p.Ile138Thr) n.3880T>C c.2957T>C (p.Ile986Thr) n.4737T>C n.4720T>C | |
| 12 | g.45852712T>G | CA384492041 | ARID2 | c.4589T>G (p.Ile1530Ser) c.798T>G c.4510T>G c.4142T>G (p.Ile1381Ser) c.3419T>G (p.Ile1140Ser) c.413T>G (p.Ile138Ser) n.3880T>G c.2957T>G (p.Ile986Ser) n.4737T>G n.4720T>G | |
| 12 | g.45852713T>A | CA479694111 | ARID2 | c.4590T>A (p.Ile1530=) c.799T>A c.4511T>A c.4143T>A (p.Ile1381=) c.3420T>A (p.Ile1140=) c.414T>A (p.Ile138=) n.3881T>A c.2958T>A (p.Ile986=) n.4738T>A n.4721T>A | |
| 12 | g.45852713T>C | CA479694112 | ARID2 | c.4590T>C (p.Ile1530=) c.799T>C c.4511T>C c.4143T>C (p.Ile1381=) c.3420T>C (p.Ile1140=) c.414T>C (p.Ile138=) n.3881T>C c.2958T>C (p.Ile986=) n.4738T>C n.4721T>C | |
| 12 | g.45852713T>G | CA384492042 | ARID2 | c.4590T>G (p.Ile1530Met) c.799T>G c.4511T>G c.4143T>G (p.Ile1381Met) c.3420T>G (p.Ile1140Met) c.414T>G (p.Ile138Met) n.3881T>G c.2958T>G (p.Ile986Met) n.4738T>G n.4721T>G | |
| 12 | g.45852714C>A | CA384492043 | ARID2 | c.4591C>A (p.Pro1531Thr) c.800C>A c.4512C>A c.4144C>A (p.Pro1382Thr) c.3421C>A (p.Pro1141Thr) c.415C>A (p.Pro139Thr) n.3882C>A c.2959C>A (p.Pro987Thr) n.4739C>A n.4722C>A | dbSNP |
| 12 | g.45852714C= | CA2033475744 | ARID2 | c.4591C= (p.Pro1531=) c.800C= c.4512C= c.4144C= (p.Pro1382=) c.3421C= (p.Pro1141=) c.415C= (p.Pro139=) n.3882C= c.2959C= (p.Pro987=) n.4739C= n.4722C= | |
| 12 | g.45852714C>G | CA384492045 | ARID2 | c.4591C>G (p.Pro1531Ala) c.800C>G c.4512C>G c.4144C>G (p.Pro1382Ala) c.3421C>G (p.Pro1141Ala) c.415C>G (p.Pro139Ala) n.3882C>G c.2959C>G (p.Pro987Ala) n.4739C>G n.4722C>G | dbSNP |
| 12 | g.45852714C>T | CA384492044 | ARID2 | c.4591C>T (p.Pro1531Ser) c.800C>T c.4512C>T c.4144C>T (p.Pro1382Ser) c.3421C>T (p.Pro1141Ser) c.415C>T (p.Pro139Ser) n.3882C>T c.2959C>T (p.Pro987Ser) n.4739C>T n.4722C>T | dbSNP COSMIC |
| 12 | g.45852715C>A | CA384492046 | ARID2 | c.4592C>A (p.Pro1531Gln) c.801C>A c.4513C>A c.4145C>A (p.Pro1382Gln) c.3422C>A (p.Pro1141Gln) c.416C>A (p.Pro139Gln) n.3883C>A c.2960C>A (p.Pro987Gln) n.4740C>A n.4723C>A | |
| 12 | g.45852715C>G | CA384492048 | ARID2 | c.4592C>G (p.Pro1531Arg) c.801C>G c.4513C>G c.4145C>G (p.Pro1382Arg) c.3422C>G (p.Pro1141Arg) c.416C>G (p.Pro139Arg) n.3883C>G c.2960C>G (p.Pro987Arg) n.4740C>G n.4723C>G | |
| 12 | g.45852715C>T | CA384492047 | ARID2 | c.4592C>T (p.Pro1531Leu) c.801C>T c.4513C>T c.4145C>T (p.Pro1382Leu) c.3422C>T (p.Pro1141Leu) c.416C>T (p.Pro139Leu) n.3883C>T c.2960C>T (p.Pro987Leu) n.4740C>T n.4723C>T | dbSNP |
| 12 | g.45852716A>C | CA479694113 | ARID2 | c.4593A>C (p.Pro1531=) c.802A>C c.4514A>C c.4146A>C (p.Pro1382=) c.3423A>C (p.Pro1141=) c.417A>C (p.Pro139=) n.3884A>C c.2961A>C (p.Pro987=) n.4741A>C n.4724A>C | |
| 12 | g.45852716A>G | CA479694114 | ARID2 | c.4593A>G (p.Pro1531=) c.802A>G c.4514A>G c.4146A>G (p.Pro1382=) c.3423A>G (p.Pro1141=) c.417A>G (p.Pro139=) n.3884A>G c.2961A>G (p.Pro987=) n.4741A>G n.4724A>G | dbSNP |
| 12 | g.45852716A>T | CA479694115 | ARID2 | c.4593A>T (p.Pro1531=) c.802A>T c.4514A>T c.4146A>T (p.Pro1382=) c.3423A>T (p.Pro1141=) c.417A>T (p.Pro139=) n.3884A>T c.2961A>T (p.Pro987=) n.4741A>T n.4724A>T | dbSNP |
| 12 | g.45852717A= | CA2033475745 | ARID2 | c.4594A= (p.Asn1532=) c.803A= c.4515A= c.4147A= (p.Asn1383=) c.3424A= (p.Asn1142=) c.418A= (p.Asn140=) n.3885A= c.2962A= (p.Asn988=) n.4742A= n.4725A= | |
| 12 | g.45852717A>C | CA384492049 | ARID2 | c.4594A>C (p.Asn1532His) c.803A>C c.4515A>C c.4147A>C (p.Asn1383His) c.3424A>C (p.Asn1142His) c.418A>C (p.Asn140His) n.3885A>C c.2962A>C (p.Asn988His) n.4742A>C n.4725A>C | dbSNP |
| 12 | g.45852717A>G | CA384492050 | ARID2 | c.4594A>G (p.Asn1532Asp) c.803A>G c.4515A>G c.4147A>G (p.Asn1383Asp) c.3424A>G (p.Asn1142Asp) c.418A>G (p.Asn140Asp) n.3885A>G c.2962A>G (p.Asn988Asp) n.4742A>G n.4725A>G | |
| 12 | g.45852717A>T | CA384492051 | ARID2 | c.4594A>T (p.Asn1532Tyr) c.803A>T c.4515A>T c.4147A>T (p.Asn1383Tyr) c.3424A>T (p.Asn1142Tyr) c.418A>T (p.Asn140Tyr) n.3885A>T c.2962A>T (p.Asn988Tyr) n.4742A>T n.4725A>T | dbSNP |
| 12 | g.45852718A>C | CA384492052 | ARID2 | c.4595A>C (p.Asn1532Thr) c.804A>C c.4516A>C c.4148A>C (p.Asn1383Thr) c.3425A>C (p.Asn1142Thr) c.419A>C (p.Asn140Thr) n.3886A>C c.2963A>C (p.Asn988Thr) n.4743A>C n.4726A>C | |
| 12 | g.45852718A>G | CA384492053 | ARID2 | c.4595A>G (p.Asn1532Ser) c.804A>G c.4516A>G c.4148A>G (p.Asn1383Ser) c.3425A>G (p.Asn1142Ser) c.419A>G (p.Asn140Ser) n.3886A>G c.2963A>G (p.Asn988Ser) n.4743A>G n.4726A>G | |
| 12 | g.45852718A>T | CA384492054 | ARID2 | c.4595A>T (p.Asn1532Ile) c.804A>T c.4516A>T c.4148A>T (p.Asn1383Ile) c.3425A>T (p.Asn1142Ile) c.419A>T (p.Asn140Ile) n.3886A>T c.2963A>T (p.Asn988Ile) n.4743A>T n.4726A>T | dbSNP |
| 12 | g.45852719T>A | CA384492055 | ARID2 | c.4596T>A (p.Asn1532Lys) c.805T>A c.4517T>A c.4149T>A (p.Asn1383Lys) c.3426T>A (p.Asn1142Lys) c.420T>A (p.Asn140Lys) n.3887T>A c.2964T>A (p.Asn988Lys) n.4744T>A n.4727T>A | dbSNP |
| 12 | g.45852719T>C | CA479694116 | ARID2 | c.4596T>C (p.Asn1532=) c.805T>C c.4517T>C c.4149T>C (p.Asn1383=) c.3426T>C (p.Asn1142=) c.420T>C (p.Asn140=) n.3887T>C c.2964T>C (p.Asn988=) n.4744T>C n.4727T>C | dbSNP |
| 12 | g.45852719T>G | CA384492056 | ARID2 | c.4596T>G (p.Asn1532Lys) c.805T>G c.4517T>G c.4149T>G (p.Asn1383Lys) c.3426T>G (p.Asn1142Lys) c.420T>G (p.Asn140Lys) n.3887T>G c.2964T>G (p.Asn988Lys) n.4744T>G n.4727T>G | dbSNP |
| 12 | g.45852720A>C | CA384492057 | ARID2 | c.4597A>C (p.Lys1533Gln) c.806A>C c.4518A>C c.4150A>C (p.Lys1384Gln) c.3427A>C (p.Lys1143Gln) c.421A>C (p.Lys141Gln) n.3888A>C c.2965A>C (p.Lys989Gln) n.4745A>C n.4728A>C | |
| 12 | g.45852720A>G | CA384492058 | ARID2 | c.4597A>G (p.Lys1533Glu) c.806A>G c.4518A>G c.4150A>G (p.Lys1384Glu) c.3427A>G (p.Lys1143Glu) c.421A>G (p.Lys141Glu) n.3888A>G c.2965A>G (p.Lys989Glu) n.4745A>G n.4728A>G | |
| 12 | g.45852720A>T | CA384492059 | ARID2 | c.4597A>T (p.Lys1533Ter) c.806A>T c.4518A>T c.4150A>T (p.Lys1384Ter) c.3427A>T (p.Lys1143Ter) c.421A>T (p.Lys141Ter) n.3888A>T c.2965A>T (p.Lys989Ter) n.4745A>T n.4728A>T | dbSNP |
| 12 | g.45852721A>C | CA384492062 | ARID2 | c.4598A>C (p.Lys1533Thr) c.807A>C c.4519A>C c.4151A>C (p.Lys1384Thr) c.3428A>C (p.Lys1143Thr) c.422A>C (p.Lys141Thr) n.3889A>C c.2966A>C (p.Lys989Thr) n.4746A>C n.4729A>C | |
| 12 | g.45852721A>G | CA384492060 | ARID2 | c.4598A>G (p.Lys1533Arg) c.807A>G c.4519A>G c.4151A>G (p.Lys1384Arg) c.3428A>G (p.Lys1143Arg) c.422A>G (p.Lys141Arg) n.3889A>G c.2966A>G (p.Lys989Arg) n.4746A>G n.4729A>G | dbSNP |
| 12 | g.45852721A>T | CA384492061 | ARID2 | c.4598A>T (p.Lys1533Ile) c.807A>T c.4519A>T c.4151A>T (p.Lys1384Ile) c.3428A>T (p.Lys1143Ile) c.422A>T (p.Lys141Ile) n.3889A>T c.2966A>T (p.Lys989Ile) n.4746A>T n.4729A>T | dbSNP |
| 12 | g.45852722A>C | CA384492063 | ARID2 | c.4599A>C (p.Lys1533Asn) c.808A>C c.4520A>C c.4152A>C (p.Lys1384Asn) c.3429A>C (p.Lys1143Asn) c.423A>C (p.Lys141Asn) n.3890A>C c.2967A>C (p.Lys989Asn) n.4747A>C n.4730A>C | |
| 12 | g.45852722A>G | CA479694117 | ARID2 | c.4599A>G (p.Lys1533=) c.808A>G c.4520A>G c.4152A>G (p.Lys1384=) c.3429A>G (p.Lys1143=) c.423A>G (p.Lys141=) n.3890A>G c.2967A>G (p.Lys989=) n.4747A>G n.4730A>G | |
| 12 | g.45852722A>T | CA384492064 | ARID2 | c.4599A>T (p.Lys1533Asn) c.808A>T c.4520A>T c.4152A>T (p.Lys1384Asn) c.3429A>T (p.Lys1143Asn) c.423A>T (p.Lys141Asn) n.3890A>T c.2967A>T (p.Lys989Asn) n.4747A>T n.4730A>T | dbSNP |
| 12 | g.45852723G>A | CA384492065 | ARID2 | c.4600G>A (p.Val1534Ile) c.809G>A c.4521G>A c.4153G>A (p.Val1385Ile) c.3430G>A (p.Val1144Ile) c.424G>A (p.Val142Ile) n.3891G>A c.2968G>A (p.Val990Ile) n.4748G>A n.4731G>A | dbSNP |
| 12 | g.45852723G>C | CA384492066 | ARID2 | c.4600G>C (p.Val1534Leu) c.809G>C c.4521G>C c.4153G>C (p.Val1385Leu) c.3430G>C (p.Val1144Leu) c.424G>C (p.Val142Leu) n.3891G>C c.2968G>C (p.Val990Leu) n.4748G>C n.4731G>C | dbSNP |
| 12 | g.45852723G>T | CA384492067 | ARID2 | c.4600G>T (p.Val1534Leu) c.809G>T c.4521G>T c.4153G>T (p.Val1385Leu) c.3430G>T (p.Val1144Leu) c.424G>T (p.Val142Leu) n.3891G>T c.2968G>T (p.Val990Leu) n.4748G>T n.4731G>T | dbSNP |
| 12 | g.45852724T>A | CA384492068 | ARID2 | c.4601T>A (p.Val1534Glu) c.810T>A c.4522T>A c.4154T>A (p.Val1385Glu) c.3431T>A (p.Val1144Glu) c.425T>A (p.Val142Glu) n.3892T>A c.2969T>A (p.Val990Glu) n.4749T>A n.4732T>A | dbSNP |
| 12 | g.45852724T>C | CA384492069 | ARID2 | c.4601T>C (p.Val1534Ala) c.810T>C c.4522T>C c.4154T>C (p.Val1385Ala) c.3431T>C (p.Val1144Ala) c.425T>C (p.Val142Ala) n.3892T>C c.2969T>C (p.Val990Ala) n.4749T>C n.4732T>C | dbSNP |
| 12 | g.45852724T>G | CA384492070 | ARID2 | c.4601T>G (p.Val1534Gly) c.810T>G c.4522T>G c.4154T>G (p.Val1385Gly) c.3431T>G (p.Val1144Gly) c.425T>G (p.Val142Gly) n.3892T>G c.2969T>G (p.Val990Gly) n.4749T>G n.4732T>G | |
| 12 | g.45852725A>C | CA479694118 | ARID2 | c.4602A>C (p.Val1534=) c.811A>C c.4523A>C c.4155A>C (p.Val1385=) c.3432A>C (p.Val1144=) c.426A>C (p.Val142=) n.3893A>C c.2970A>C (p.Val990=) n.4750A>C n.4733A>C | |
| 12 | g.45852725A>G | CA479694119 | ARID2 | c.4602A>G (p.Val1534=) c.811A>G c.4523A>G c.4155A>G (p.Val1385=) c.3432A>G (p.Val1144=) c.426A>G (p.Val142=) n.3893A>G c.2970A>G (p.Val990=) n.4750A>G n.4733A>G | |
| 12 | g.45852725A>T | CA479694120 | ARID2 | c.4602A>T (p.Val1534=) c.811A>T c.4523A>T c.4155A>T (p.Val1385=) c.3432A>T (p.Val1144=) c.426A>T (p.Val142=) n.3893A>T c.2970A>T (p.Val990=) n.4750A>T n.4733A>T | dbSNP |
| 12 | g.45852726G>A | CA384492071 | ARID2 | c.4603G>A (p.Gly1535Arg) c.812G>A c.4524G>A c.4156G>A (p.Gly1386Arg) c.3433G>A (p.Gly1145Arg) c.427G>A (p.Gly143Arg) n.3894G>A c.2971G>A (p.Gly991Arg) n.4751G>A n.4734G>A | dbSNP |
| 12 | g.45852726G>C | CA384492072 | ARID2 | c.4603G>C (p.Gly1535Arg) c.812G>C c.4524G>C c.4156G>C (p.Gly1386Arg) c.3433G>C (p.Gly1145Arg) c.427G>C (p.Gly143Arg) n.3894G>C c.2971G>C (p.Gly991Arg) n.4751G>C n.4734G>C | dbSNP |
| 12 | g.45852726G= | CA2033475746 | ARID2 | c.4603G= (p.Gly1535=) c.812G= c.4524G= c.4156G= (p.Gly1386=) c.3433G= (p.Gly1145=) c.427G= (p.Gly143=) n.3894G= c.2971G= (p.Gly991=) n.4751G= n.4734G= | |
| 12 | g.45852726G>T | CA384492073 | ARID2 | c.4603G>T (p.Gly1535Ter) c.812G>T c.4524G>T c.4156G>T (p.Gly1386Ter) c.3433G>T (p.Gly1145Ter) c.427G>T (p.Gly143Ter) n.3894G>T c.2971G>T (p.Gly991Ter) n.4751G>T n.4734G>T | dbSNP COSMIC |
| 12 | g.45852727G>A | CA384492075 | ARID2 | c.4604G>A (p.Gly1535Glu) c.813G>A c.4525G>A c.4157G>A (p.Gly1386Glu) c.3434G>A (p.Gly1145Glu) c.428G>A (p.Gly143Glu) n.3895G>A c.2972G>A (p.Gly991Glu) n.4752G>A n.4735G>A | dbSNP |
| 12 | g.45852727G>C | CA384492076 | ARID2 | c.4604G>C (p.Gly1535Ala) c.813G>C c.4525G>C c.4157G>C (p.Gly1386Ala) c.3434G>C (p.Gly1145Ala) c.428G>C (p.Gly143Ala) n.3895G>C c.2972G>C (p.Gly991Ala) n.4752G>C n.4735G>C | |
| 12 | g.45852727G= | CA2033475747 | ARID2 | c.4604G= (p.Gly1535=) c.813G= c.4525G= c.4157G= (p.Gly1386=) c.3434G= (p.Gly1145=) c.428G= (p.Gly143=) n.3895G= c.2972G= (p.Gly991=) n.4752G= n.4735G= | |
| 12 | g.45852727G>T | CA384492074 | ARID2 | c.4604G>T (p.Gly1535Val) c.813G>T c.4525G>T c.4157G>T (p.Gly1386Val) c.3434G>T (p.Gly1145Val) c.428G>T (p.Gly143Val) n.3895G>T c.2972G>T (p.Gly991Val) n.4752G>T n.4735G>T | |
| 12 | g.45852728A>C | CA479694121 | ARID2 | c.4605A>C (p.Gly1535=) c.814A>C c.4526A>C c.4158A>C (p.Gly1386=) c.3435A>C (p.Gly1145=) c.429A>C (p.Gly143=) n.3896A>C c.2973A>C (p.Gly991=) n.4753A>C n.4736A>C | |
| 12 | g.45852728A>G | CA479694122 | ARID2 | c.4605A>G (p.Gly1535=) c.814A>G c.4526A>G c.4158A>G (p.Gly1386=) c.3435A>G (p.Gly1145=) c.429A>G (p.Gly143=) n.3896A>G c.2973A>G (p.Gly991=) n.4753A>G n.4736A>G | dbSNP |
| 12 | g.45852728A>T | CA479694123 | ARID2 | c.4605A>T (p.Gly1535=) c.814A>T c.4526A>T c.4158A>T (p.Gly1386=) c.3435A>T (p.Gly1145=) c.429A>T (p.Gly143=) n.3896A>T c.2973A>T (p.Gly991=) n.4753A>T n.4736A>T | dbSNP |
| 12 | g.45852729G>A | CA384492077 | ARID2 | c.4606G>A (p.Val1536Ile) c.815G>A c.4527G>A c.4159G>A (p.Val1387Ile) c.3436G>A (p.Val1146Ile) c.430G>A (p.Val144Ile) n.3897G>A c.2974G>A (p.Val992Ile) n.4754G>A n.4737G>A | |
| 12 | g.45852729G>C | CA384492078 | ARID2 | c.4606G>C (p.Val1536Leu) c.815G>C c.4527G>C c.4159G>C (p.Val1387Leu) c.3436G>C (p.Val1146Leu) c.430G>C (p.Val144Leu) n.3897G>C c.2974G>C (p.Val992Leu) n.4754G>C n.4737G>C | |
| 12 | g.45852729G>T | CA384492079 | ARID2 | c.4606G>T (p.Val1536Phe) c.815G>T c.4527G>T c.4159G>T (p.Val1387Phe) c.3436G>T (p.Val1146Phe) c.430G>T (p.Val144Phe) n.3897G>T c.2974G>T (p.Val992Phe) n.4754G>T n.4737G>T | |
| 12 | g.45852730T>A | CA384492080 | ARID2 | c.4607T>A (p.Val1536Asp) c.816T>A c.4528T>A c.4160T>A (p.Val1387Asp) c.3437T>A (p.Val1146Asp) c.431T>A (p.Val144Asp) n.3898T>A c.2975T>A (p.Val992Asp) n.4755T>A n.4738T>A | |
| 12 | g.45852730T>C | CA384492081 | ARID2 | c.4607T>C (p.Val1536Ala) c.816T>C c.4528T>C c.4160T>C (p.Val1387Ala) c.3437T>C (p.Val1146Ala) c.431T>C (p.Val144Ala) n.3898T>C c.2975T>C (p.Val992Ala) n.4755T>C n.4738T>C | |
| 12 | g.45852730T>G | CA384492082 | ARID2 | c.4607T>G (p.Val1536Gly) c.816T>G c.4528T>G c.4160T>G (p.Val1387Gly) c.3437T>G (p.Val1146Gly) c.431T>G (p.Val144Gly) n.3898T>G c.2975T>G (p.Val992Gly) n.4755T>G n.4738T>G | dbSNP |
| 12 | g.45852731T>A | CA479694124 | ARID2 | c.4608T>A (p.Val1536=) c.817T>A c.4529T>A c.4161T>A (p.Val1387=) c.3438T>A (p.Val1146=) c.432T>A (p.Val144=) n.3899T>A c.2976T>A (p.Val992=) n.4756T>A n.4739T>A | dbSNP |
| 12 | g.45852731T>C | CA479694126 | ARID2 | c.4608T>C (p.Val1536=) c.817T>C c.4529T>C c.4161T>C (p.Val1387=) c.3438T>C (p.Val1146=) c.432T>C (p.Val144=) n.3899T>C c.2976T>C (p.Val992=) n.4756T>C n.4739T>C | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852731T>G | CA479694125 | ARID2 | c.4608T>G (p.Val1536=) c.817T>G c.4529T>G c.4161T>G (p.Val1387=) c.3438T>G (p.Val1146=) c.432T>G (p.Val144=) n.3899T>G c.2976T>G (p.Val992=) n.4756T>G n.4739T>G | dbSNP |
| 12 | g.45852731T= | CA2033475748 | ARID2 | c.4608T= (p.Val1536=) c.817T= c.4529T= c.4161T= (p.Val1387=) c.3438T= (p.Val1146=) c.432T= (p.Val144=) n.3899T= c.2976T= (p.Val992=) n.4756T= n.4739T= | |
| 12 | g.45852732A>C | CA479694127 | ARID2 | c.4609A>C (p.Arg1537=) c.818A>C c.4530A>C c.4162A>C (p.Arg1388=) c.3439A>C (p.Arg1147=) c.433A>C (p.Arg145=) n.3900A>C c.2977A>C (p.Arg993=) n.4757A>C n.4740A>C | |
| 12 | g.45852732A>G | CA384492083 | ARID2 | c.4609A>G (p.Arg1537Gly) c.818A>G c.4530A>G c.4162A>G (p.Arg1388Gly) c.3439A>G (p.Arg1147Gly) c.433A>G (p.Arg145Gly) n.3900A>G c.2977A>G (p.Arg993Gly) n.4757A>G n.4740A>G | dbSNP gnomAD v4 |
| 12 | g.45852732A>T | CA384492084 | ARID2 | c.4609A>T (p.Arg1537Ter) c.818A>T c.4530A>T c.4162A>T (p.Arg1388Ter) c.3439A>T (p.Arg1147Ter) c.433A>T (p.Arg145Ter) n.3900A>T c.2977A>T (p.Arg993Ter) n.4757A>T n.4740A>T | dbSNP |
| 12 | g.45852732dup | CA645571104 | ARID2 | c.4609dup (p.Arg1537LysfsTer7) c.818dup c.4530dup c.4162dup (p.Arg1388LysfsTer7) c.3439dup (p.Arg1147LysfsTer7) c.433dup (p.Arg145LysfsTer7) n.3900dup c.2977dup (p.Arg993LysfsTer7) n.4757dup n.4740dup | COSMIC |
| 12 | g.45852733G>A | CA384492085 | ARID2 | c.4610G>A (p.Arg1537Lys) c.819G>A c.4531G>A c.4163G>A (p.Arg1388Lys) c.3440G>A (p.Arg1147Lys) c.434G>A (p.Arg145Lys) n.3901G>A c.2978G>A (p.Arg993Lys) n.4758G>A n.4741G>A | dbSNP |
| 12 | g.45852733G>C | CA384492086 | ARID2 | c.4610G>C (p.Arg1537Thr) c.819G>C c.4531G>C c.4163G>C (p.Arg1388Thr) c.3440G>C (p.Arg1147Thr) c.434G>C (p.Arg145Thr) n.3901G>C c.2978G>C (p.Arg993Thr) n.4758G>C n.4741G>C | dbSNP |
| 12 | g.45852733G>T | CA384492087 | ARID2 | c.4610G>T (p.Arg1537Ile) c.819G>T c.4531G>T c.4163G>T (p.Arg1388Ile) c.3440G>T (p.Arg1147Ile) c.434G>T (p.Arg145Ile) n.3901G>T c.2978G>T (p.Arg993Ile) n.4758G>T n.4741G>T | |
| 12 | g.45852734A= | CA2033475749 | ARID2 | c.4611A= (p.Arg1537=) c.820A= c.4532A= c.4164A= (p.Arg1388=) c.3441A= (p.Arg1147=) c.435A= (p.Arg145=) n.3902A= c.2979A= (p.Arg993=) n.4759A= n.4742A= | |
| 12 | g.45852734A>C | CA384492088 | ARID2 | c.4611A>C (p.Arg1537Ser) c.820A>C c.4532A>C c.4164A>C (p.Arg1388Ser) c.3441A>C (p.Arg1147Ser) c.435A>C (p.Arg145Ser) n.3902A>C c.2979A>C (p.Arg993Ser) n.4759A>C n.4742A>C | |
| 12 | g.45852734A>G | CA479694128 | ARID2 | c.4611A>G (p.Arg1537=) c.820A>G c.4532A>G c.4164A>G (p.Arg1388=) c.3441A>G (p.Arg1147=) c.435A>G (p.Arg145=) n.3902A>G c.2979A>G (p.Arg993=) n.4759A>G n.4742A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852734A>T | CA384492089 | ARID2 | c.4611A>T (p.Arg1537Ser) c.820A>T c.4532A>T c.4164A>T (p.Arg1388Ser) c.3441A>T (p.Arg1147Ser) c.435A>T (p.Arg145Ser) n.3902A>T c.2979A>T (p.Arg993Ser) n.4759A>T n.4742A>T | dbSNP |
| 12 | g.45852735A= | CA2033475750 | ARID2 | c.4612A= (p.Ile1538=) c.821A= c.4533A= c.4165A= (p.Ile1389=) c.3442A= (p.Ile1148=) c.436A= (p.Ile146=) n.3903A= c.2980A= (p.Ile994=) n.4760A= n.4743A= | |
| 12 | g.45852735A>C | CA384492092 | ARID2 | c.4612A>C (p.Ile1538Leu) c.821A>C c.4533A>C c.4165A>C (p.Ile1389Leu) c.3442A>C (p.Ile1148Leu) c.436A>C (p.Ile146Leu) n.3903A>C c.2980A>C (p.Ile994Leu) n.4760A>C n.4743A>C | dbSNP |
| 12 | g.45852735A>G | CA384492091 | ARID2 | c.4612A>G (p.Ile1538Val) c.821A>G c.4533A>G c.4165A>G (p.Ile1389Val) c.3442A>G (p.Ile1148Val) c.436A>G (p.Ile146Val) n.3903A>G c.2980A>G (p.Ile994Val) n.4760A>G n.4743A>G | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852735A>T | CA384492090 | ARID2 | c.4612A>T (p.Ile1538Phe) c.821A>T c.4533A>T c.4165A>T (p.Ile1389Phe) c.3442A>T (p.Ile1148Phe) c.436A>T (p.Ile146Phe) n.3903A>T c.2980A>T (p.Ile994Phe) n.4760A>T n.4743A>T | dbSNP |
| 12 | g.45852736T>A | CA384492093 | ARID2 | c.4613T>A (p.Ile1538Asn) c.822T>A c.4534T>A c.4166T>A (p.Ile1389Asn) c.3443T>A (p.Ile1148Asn) c.437T>A (p.Ile146Asn) n.3904T>A c.2981T>A (p.Ile994Asn) n.4761T>A n.4744T>A | dbSNP |
| 12 | g.45852736T>C | CA384492094 | ARID2 | c.4613T>C (p.Ile1538Thr) c.822T>C c.4534T>C c.4166T>C (p.Ile1389Thr) c.3443T>C (p.Ile1148Thr) c.437T>C (p.Ile146Thr) n.3904T>C c.2981T>C (p.Ile994Thr) n.4761T>C n.4744T>C | |
| 12 | g.45852736T>G | CA384492095 | ARID2 | c.4613T>G (p.Ile1538Ser) c.822T>G c.4534T>G c.4166T>G (p.Ile1389Ser) c.3443T>G (p.Ile1148Ser) c.437T>G (p.Ile146Ser) n.3904T>G c.2981T>G (p.Ile994Ser) n.4761T>G n.4744T>G | |
| 12 | g.45852737del | CA479694129 | ARID2 | c.4614del (p.Ile1538MetfsTer28) c.823del c.4535del c.4167del (p.Ile1389MetfsTer28) c.3444del (p.Ile1148MetfsTer28) c.438del (p.Ile146MetfsTer28) n.3905del c.2982del (p.Ile994MetfsTer28) n.4762del n.4745del | COSMIC |
| 12 | g.45852737T>A | CA479694130 | ARID2 | c.4614T>A (p.Ile1538=) c.823T>A c.4535T>A c.4167T>A (p.Ile1389=) c.3444T>A (p.Ile1148=) c.438T>A (p.Ile146=) n.3905T>A c.2982T>A (p.Ile994=) n.4762T>A n.4745T>A | dbSNP |
| 12 | g.45852737T>C | CA479694131 | ARID2 | c.4614T>C (p.Ile1538=) c.823T>C c.4535T>C c.4167T>C (p.Ile1389=) c.3444T>C (p.Ile1148=) c.438T>C (p.Ile146=) n.3905T>C c.2982T>C (p.Ile994=) n.4762T>C n.4745T>C | dbSNP |
| 12 | g.45852737T>G | CA384492096 | ARID2 | c.4614T>G (p.Ile1538Met) c.823T>G c.4535T>G c.4167T>G (p.Ile1389Met) c.3444T>G (p.Ile1148Met) c.438T>G (p.Ile146Met) n.3905T>G c.2982T>G (p.Ile994Met) n.4762T>G n.4745T>G | |
| 12 | g.45852738G>A | CA384492097 | ARID2 | c.4615G>A (p.Val1539Ile) c.824G>A c.4536G>A c.4168G>A (p.Val1390Ile) c.3445G>A (p.Val1149Ile) c.439G>A (p.Val147Ile) n.3906G>A c.2983G>A (p.Val995Ile) n.4763G>A n.4746G>A | dbSNP |
| 12 | g.45852738G>C | CA384492098 | ARID2 | c.4615G>C (p.Val1539Leu) c.824G>C c.4536G>C c.4168G>C (p.Val1390Leu) c.3445G>C (p.Val1149Leu) c.439G>C (p.Val147Leu) n.3906G>C c.2983G>C (p.Val995Leu) n.4763G>C n.4746G>C | |
| 12 | g.45852738G= | CA2033475751 | ARID2 | c.4615G= (p.Val1539=) c.824G= c.4536G= c.4168G= (p.Val1390=) c.3445G= (p.Val1149=) c.439G= (p.Val147=) n.3906G= c.2983G= (p.Val995=) n.4763G= n.4746G= | |
| 12 | g.45852738G>T | CA384492099 | ARID2 | c.4615G>T (p.Val1539Phe) c.824G>T c.4536G>T c.4168G>T (p.Val1390Phe) c.3445G>T (p.Val1149Phe) c.439G>T (p.Val147Phe) n.3906G>T c.2983G>T (p.Val995Phe) n.4763G>T n.4746G>T | |
| 12 | g.45852739T>A | CA384492100 | ARID2 | c.4616T>A (p.Val1539Asp) c.825T>A c.4537T>A c.4169T>A (p.Val1390Asp) c.3446T>A (p.Val1149Asp) c.440T>A (p.Val147Asp) n.3907T>A c.2984T>A (p.Val995Asp) n.4764T>A n.4747T>A | dbSNP gnomAD v4 |
| 12 | g.45852739T>C | CA384492101 | ARID2 | c.4616T>C (p.Val1539Ala) c.825T>C c.4537T>C c.4169T>C (p.Val1390Ala) c.3446T>C (p.Val1149Ala) c.440T>C (p.Val147Ala) n.3907T>C c.2984T>C (p.Val995Ala) n.4764T>C n.4747T>C | gnomAD v4 |
| 12 | g.45852739T>G | CA384492102 | ARID2 | c.4616T>G (p.Val1539Gly) c.825T>G c.4537T>G c.4169T>G (p.Val1390Gly) c.3446T>G (p.Val1149Gly) c.440T>G (p.Val147Gly) n.3907T>G c.2984T>G (p.Val995Gly) n.4764T>G n.4747T>G | |
| 12 | g.45852740T>A | CA479694134 | ARID2 | c.4617T>A (p.Val1539=) c.826T>A c.4538T>A c.4170T>A (p.Val1390=) c.3447T>A (p.Val1149=) c.441T>A (p.Val147=) n.3908T>A c.2985T>A (p.Val995=) n.4765T>A n.4748T>A | dbSNP |
| 12 | g.45852740T>C | CA479694133 | ARID2 | c.4617T>C (p.Val1539=) c.826T>C c.4538T>C c.4170T>C (p.Val1390=) c.3447T>C (p.Val1149=) c.441T>C (p.Val147=) n.3908T>C c.2985T>C (p.Val995=) n.4765T>C n.4748T>C | gnomAD v4 |
| 12 | g.45852740T>G | CA479694132 | ARID2 | c.4617T>G (p.Val1539=) c.826T>G c.4538T>G c.4170T>G (p.Val1390=) c.3447T>G (p.Val1149=) c.441T>G (p.Val147=) n.3908T>G c.2985T>G (p.Val995=) n.4765T>G n.4748T>G | |
| 12 | g.45852741A= | CA2033475752 | ARID2 | c.4618A= (p.Thr1540=) c.827A= c.4539A= c.4171A= (p.Thr1391=) c.3448A= (p.Thr1150=) c.442A= (p.Thr148=) n.3909A= c.2986A= (p.Thr996=) n.4766A= n.4749A= | |
| 12 | g.45852741A>C | CA384492103 | ARID2 | c.4618A>C (p.Thr1540Pro) c.827A>C c.4539A>C c.4171A>C (p.Thr1391Pro) c.3448A>C (p.Thr1150Pro) c.442A>C (p.Thr148Pro) n.3909A>C c.2986A>C (p.Thr996Pro) n.4766A>C n.4749A>C | dbSNP |
| 12 | g.45852741A>G | CA384492104 | ARID2 | c.4618A>G (p.Thr1540Ala) c.827A>G c.4539A>G c.4171A>G (p.Thr1391Ala) c.3448A>G (p.Thr1150Ala) c.442A>G (p.Thr148Ala) n.3909A>G c.2986A>G (p.Thr996Ala) n.4766A>G n.4749A>G | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852741A>T | CA384492105 | ARID2 | c.4618A>T (p.Thr1540Ser) c.827A>T c.4539A>T c.4171A>T (p.Thr1391Ser) c.3448A>T (p.Thr1150Ser) c.442A>T (p.Thr148Ser) n.3909A>T c.2986A>T (p.Thr996Ser) n.4766A>T n.4749A>T | dbSNP |
| 12 | g.45852741dup | CA2618443393 | ARID2 | c.4618dup (p.Thr1540AsnfsTer4) c.827dup c.4539dup c.4171dup (p.Thr1391AsnfsTer4) c.3448dup (p.Thr1150AsnfsTer4) c.442dup (p.Thr148AsnfsTer4) n.3909dup c.2986dup (p.Thr996AsnfsTer4) n.4766dup n.4749dup | gnomAD v4 |
| 12 | g.45852742C>A | CA6526695 | ARID2 | c.4619C>A (p.Thr1540Lys) c.828C>A c.4540C>A c.4172C>A (p.Thr1391Lys) c.3449C>A (p.Thr1150Lys) c.443C>A (p.Thr148Lys) n.3910C>A c.2987C>A (p.Thr996Lys) n.4767C>A n.4750C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852742C= | CA2033475753 | ARID2 | c.4619C= (p.Thr1540=) c.828C= c.4540C= c.4172C= (p.Thr1391=) c.3449C= (p.Thr1150=) c.443C= (p.Thr148=) n.3910C= c.2987C= (p.Thr996=) n.4767C= n.4750C= | |
| 12 | g.45852742C>G | CA384492107 | ARID2 | c.4619C>G (p.Thr1540Arg) c.828C>G c.4540C>G c.4172C>G (p.Thr1391Arg) c.3449C>G (p.Thr1150Arg) c.443C>G (p.Thr148Arg) n.3910C>G c.2987C>G (p.Thr996Arg) n.4767C>G n.4750C>G | dbSNP |
| 12 | g.45852742C>T | CA384492106 | ARID2 | c.4619C>T (p.Thr1540Ile) c.828C>T c.4540C>T c.4172C>T (p.Thr1391Ile) c.3449C>T (p.Thr1150Ile) c.443C>T (p.Thr148Ile) n.3910C>T c.2987C>T (p.Thr996Ile) n.4767C>T n.4750C>T | dbSNP |
| 12 | g.45852744_45852747del | CA2618443396 | ARID2 | c.4621_4624del (p.Ile1541ValfsTer24) c.830_833del c.4542_4545del c.4174_4177del (p.Ile1392ValfsTer24) c.3451_3454del (p.Ile1151ValfsTer24) c.445_448del (p.Ile149ValfsTer24) n.3912_3915del c.2989_2992del (p.Ile997ValfsTer24) n.4769_4772del n.4752_4755del | gnomAD v4 |
| 12 | g.45852743A>C | CA479694135 | ARID2 | c.4620A>C (p.Thr1540=) c.829A>C c.4541A>C c.4173A>C (p.Thr1391=) c.3450A>C (p.Thr1150=) c.444A>C (p.Thr148=) n.3911A>C c.2988A>C (p.Thr996=) n.4768A>C n.4751A>C | |
| 12 | g.45852743A>G | CA479694136 | ARID2 | c.4620A>G (p.Thr1540=) c.829A>G c.4541A>G c.4173A>G (p.Thr1391=) c.3450A>G (p.Thr1150=) c.444A>G (p.Thr148=) n.3911A>G c.2988A>G (p.Thr996=) n.4768A>G n.4751A>G | |
| 12 | g.45852743A>T | CA479694137 | ARID2 | c.4620A>T (p.Thr1540=) c.829A>T c.4541A>T c.4173A>T (p.Thr1391=) c.3450A>T (p.Thr1150=) c.444A>T (p.Thr148=) n.3911A>T c.2988A>T (p.Thr996=) n.4768A>T n.4751A>T | |
| 12 | g.45852744A= | CA2033475754 | ARID2 | c.4621A= (p.Ile1541=) c.830A= c.4542A= c.4174A= (p.Ile1392=) c.3451A= (p.Ile1151=) c.445A= (p.Ile149=) n.3912A= c.2989A= (p.Ile997=) n.4769A= n.4752A= | |
| 12 | g.45852744A>C | CA384492108 | ARID2 | c.4621A>C (p.Ile1541Leu) c.830A>C c.4542A>C c.4174A>C (p.Ile1392Leu) c.3451A>C (p.Ile1151Leu) c.445A>C (p.Ile149Leu) n.3912A>C c.2989A>C (p.Ile997Leu) n.4769A>C n.4752A>C | dbSNP |
| 12 | g.45852744A>G | CA236400883 | ARID2 | c.4621A>G (p.Ile1541Val) c.830A>G c.4542A>G c.4174A>G (p.Ile1392Val) c.3451A>G (p.Ile1151Val) c.445A>G (p.Ile149Val) n.3912A>G c.2989A>G (p.Ile997Val) n.4769A>G n.4752A>G | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852744A>T | CA384492109 | ARID2 | c.4621A>T (p.Ile1541Phe) c.830A>T c.4542A>T c.4174A>T (p.Ile1392Phe) c.3451A>T (p.Ile1151Phe) c.445A>T (p.Ile149Phe) n.3912A>T c.2989A>T (p.Ile997Phe) n.4769A>T n.4752A>T | dbSNP |
| 12 | g.45852745T>A | CA384492110 | ARID2 | c.4622T>A (p.Ile1541Asn) c.831T>A c.4543T>A c.4175T>A (p.Ile1392Asn) c.3452T>A (p.Ile1151Asn) c.446T>A (p.Ile149Asn) n.3913T>A c.2990T>A (p.Ile997Asn) n.4770T>A n.4753T>A | dbSNP |
| 12 | g.45852745T>C | CA384492112 | ARID2 | c.4622T>C (p.Ile1541Thr) c.831T>C c.4543T>C c.4175T>C (p.Ile1392Thr) c.3452T>C (p.Ile1151Thr) c.446T>C (p.Ile149Thr) n.3913T>C c.2990T>C (p.Ile997Thr) n.4770T>C n.4753T>C | dbSNP |
| 12 | g.45852745T>G | CA384492111 | ARID2 | c.4622T>G (p.Ile1541Ser) c.831T>G c.4543T>G c.4175T>G (p.Ile1392Ser) c.3452T>G (p.Ile1151Ser) c.446T>G (p.Ile149Ser) n.3913T>G c.2990T>G (p.Ile997Ser) n.4770T>G n.4753T>G | |
| 12 | g.45852746C>A | CA479694138 | ARID2 | c.4623C>A (p.Ile1541=) c.832C>A c.4544C>A c.4176C>A (p.Ile1392=) c.3453C>A (p.Ile1151=) c.447C>A (p.Ile149=) n.3914C>A c.2991C>A (p.Ile997=) n.4771C>A n.4754C>A | dbSNP |
| 12 | g.45852746C>G | CA384492113 | ARID2 | c.4623C>G (p.Ile1541Met) c.832C>G c.4544C>G c.4176C>G (p.Ile1392Met) c.3453C>G (p.Ile1151Met) c.447C>G (p.Ile149Met) n.3914C>G c.2991C>G (p.Ile997Met) n.4771C>G n.4754C>G | dbSNP |
| 12 | g.45852746C>T | CA479694139 | ARID2 | c.4623C>T (p.Ile1541=) c.832C>T c.4544C>T c.4176C>T (p.Ile1392=) c.3453C>T (p.Ile1151=) c.447C>T (p.Ile149=) n.3914C>T c.2991C>T (p.Ile997=) n.4771C>T n.4754C>T | dbSNP |
| 12 | g.45852747A>C | CA384492114 | ARID2 | c.4624A>C (p.Ser1542Arg) c.833A>C c.4545A>C c.4177A>C (p.Ser1393Arg) c.3454A>C (p.Ser1152Arg) c.448A>C (p.Ser150Arg) n.3915A>C c.2992A>C (p.Ser998Arg) n.4772A>C n.4755A>C | |
| 12 | g.45852747A>G | CA384492115 | ARID2 | c.4624A>G (p.Ser1542Gly) c.833A>G c.4545A>G c.4177A>G (p.Ser1393Gly) c.3454A>G (p.Ser1152Gly) c.448A>G (p.Ser150Gly) n.3915A>G c.2992A>G (p.Ser998Gly) n.4772A>G n.4755A>G | dbSNP |
| 12 | g.45852747A>T | CA384492116 | ARID2 | c.4624A>T (p.Ser1542Cys) c.833A>T c.4545A>T c.4177A>T (p.Ser1393Cys) c.3454A>T (p.Ser1152Cys) c.448A>T (p.Ser150Cys) n.3915A>T c.2992A>T (p.Ser998Cys) n.4772A>T n.4755A>T | dbSNP |
| 12 | g.45852748G>A | CA384492117 | ARID2 | c.4625G>A (p.Ser1542Asn) c.834G>A c.4546G>A c.4178G>A (p.Ser1393Asn) c.3455G>A (p.Ser1152Asn) c.449G>A (p.Ser150Asn) n.3916G>A c.2993G>A (p.Ser998Asn) n.4773G>A n.4756G>A | dbSNP |
| 12 | g.45852748G>C | CA384492118 | ARID2 | c.4625G>C (p.Ser1542Thr) c.834G>C c.4546G>C c.4178G>C (p.Ser1393Thr) c.3455G>C (p.Ser1152Thr) c.449G>C (p.Ser150Thr) n.3916G>C c.2993G>C (p.Ser998Thr) n.4773G>C n.4756G>C | dbSNP |
| 12 | g.45852748G= | CA2033475755 | ARID2 | c.4625G= (p.Ser1542=) c.834G= c.4546G= c.4178G= (p.Ser1393=) c.3455G= (p.Ser1152=) c.449G= (p.Ser150=) n.3916G= c.2993G= (p.Ser998=) n.4773G= n.4756G= | |
| 12 | g.45852748G>T | CA384492119 | ARID2 | c.4625G>T (p.Ser1542Ile) c.834G>T c.4546G>T c.4178G>T (p.Ser1393Ile) c.3455G>T (p.Ser1152Ile) c.449G>T (p.Ser150Ile) n.3916G>T c.2993G>T (p.Ser998Ile) n.4773G>T n.4756G>T | |
| 12 | g.45852749T>A | CA384492120 | ARID2 | c.4626T>A (p.Ser1542Arg) c.835T>A c.4547T>A c.4179T>A (p.Ser1393Arg) c.3456T>A (p.Ser1152Arg) c.450T>A (p.Ser150Arg) n.3917T>A c.2994T>A (p.Ser998Arg) n.4774T>A n.4757T>A | dbSNP |
| 12 | g.45852749T>C | CA479694140 | ARID2 | c.4626T>C (p.Ser1542=) c.835T>C c.4547T>C c.4179T>C (p.Ser1393=) c.3456T>C (p.Ser1152=) c.450T>C (p.Ser150=) n.3917T>C c.2994T>C (p.Ser998=) n.4774T>C n.4757T>C | |
| 12 | g.45852749T>G | CA384492121 | ARID2 | c.4626T>G (p.Ser1542Arg) c.835T>G c.4547T>G c.4179T>G (p.Ser1393Arg) c.3456T>G (p.Ser1152Arg) c.450T>G (p.Ser150Arg) n.3917T>G c.2994T>G (p.Ser998Arg) n.4774T>G n.4757T>G | |
| 12 | g.45852750G>A | CA384492122 | ARID2 | c.4627G>A (p.Asp1543Asn) c.836G>A c.4548G>A c.4180G>A (p.Asp1394Asn) c.3457G>A (p.Asp1153Asn) c.451G>A (p.Asp151Asn) n.3918G>A c.2995G>A (p.Asp999Asn) n.4775G>A n.4758G>A | dbSNP |
| 12 | g.45852750G>C | CA384492123 | ARID2 | c.4627G>C (p.Asp1543His) c.836G>C c.4548G>C c.4180G>C (p.Asp1394His) c.3457G>C (p.Asp1153His) c.451G>C (p.Asp151His) n.3918G>C c.2995G>C (p.Asp999His) n.4775G>C n.4758G>C | dbSNP |
| 12 | g.45852750G>T | CA384492124 | ARID2 | c.4627G>T (p.Asp1543Tyr) c.836G>T c.4548G>T c.4180G>T (p.Asp1394Tyr) c.3457G>T (p.Asp1153Tyr) c.451G>T (p.Asp151Tyr) n.3918G>T c.2995G>T (p.Asp999Tyr) n.4775G>T n.4758G>T | |
| 12 | g.45852751A>C | CA384492127 | ARID2 | c.4628A>C (p.Asp1543Ala) c.837A>C c.4549A>C c.4181A>C (p.Asp1394Ala) c.3458A>C (p.Asp1153Ala) c.452A>C (p.Asp151Ala) n.3919A>C c.2996A>C (p.Asp999Ala) n.4776A>C n.4759A>C | |
| 12 | g.45852751A>G | CA384492125 | ARID2 | c.4628A>G (p.Asp1543Gly) c.837A>G c.4549A>G c.4181A>G (p.Asp1394Gly) c.3458A>G (p.Asp1153Gly) c.452A>G (p.Asp151Gly) n.3919A>G c.2996A>G (p.Asp999Gly) n.4776A>G n.4759A>G | |
| 12 | g.45852751A>T | CA384492126 | ARID2 | c.4628A>T (p.Asp1543Val) c.837A>T c.4549A>T c.4181A>T (p.Asp1394Val) c.3458A>T (p.Asp1153Val) c.452A>T (p.Asp151Val) n.3919A>T c.2996A>T (p.Asp999Val) n.4776A>T n.4759A>T | |
| 12 | g.45852752C>A | CA384492128 | ARID2 | c.4629C>A (p.Asp1543Glu) c.838C>A c.4550C>A c.4182C>A (p.Asp1394Glu) c.3459C>A (p.Asp1153Glu) c.453C>A (p.Asp151Glu) n.3920C>A c.2997C>A (p.Asp999Glu) n.4777C>A n.4760C>A | dbSNP |
| 12 | g.45852752C>G | CA384492129 | ARID2 | c.4629C>G (p.Asp1543Glu) c.838C>G c.4550C>G c.4182C>G (p.Asp1394Glu) c.3459C>G (p.Asp1153Glu) c.453C>G (p.Asp151Glu) n.3920C>G c.2997C>G (p.Asp999Glu) n.4777C>G n.4760C>G | dbSNP |
| 12 | g.45852752C>T | CA479694141 | ARID2 | c.4629C>T (p.Asp1543=) c.838C>T c.4550C>T c.4182C>T (p.Asp1394=) c.3459C>T (p.Asp1153=) c.453C>T (p.Asp151=) n.3920C>T c.2997C>T (p.Asp999=) n.4777C>T n.4760C>T | dbSNP |
| 12 | g.45852753C>A | CA384492130 | ARID2 | c.4630C>A (p.Pro1544Thr) c.839C>A c.4551C>A c.4183C>A (p.Pro1395Thr) c.3460C>A (p.Pro1154Thr) c.454C>A (p.Pro152Thr) n.3921C>A c.2998C>A (p.Pro1000Thr) n.4778C>A n.4761C>A | dbSNP |
| 12 | g.45852753C>G | CA384492131 | ARID2 | c.4630C>G (p.Pro1544Ala) c.839C>G c.4551C>G c.4183C>G (p.Pro1395Ala) c.3460C>G (p.Pro1154Ala) c.454C>G (p.Pro152Ala) n.3921C>G c.2998C>G (p.Pro1000Ala) n.4778C>G n.4761C>G | dbSNP |
| 12 | g.45852753C>T | CA384492132 | ARID2 | c.4630C>T (p.Pro1544Ser) c.839C>T c.4551C>T c.4183C>T (p.Pro1395Ser) c.3460C>T (p.Pro1154Ser) c.454C>T (p.Pro152Ser) n.3921C>T c.2998C>T (p.Pro1000Ser) n.4778C>T n.4761C>T | dbSNP |
| 12 | g.45852754C>A | CA384492133 | ARID2 | c.4631C>A (p.Pro1544His) c.840C>A c.4552C>A c.4184C>A (p.Pro1395His) c.3461C>A (p.Pro1154His) c.455C>A (p.Pro152His) n.3922C>A c.2999C>A (p.Pro1000His) n.4779C>A n.4762C>A | dbSNP |
| 12 | g.45852754C>G | CA384492134 | ARID2 | c.4631C>G (p.Pro1544Arg) c.840C>G c.4552C>G c.4184C>G (p.Pro1395Arg) c.3461C>G (p.Pro1154Arg) c.455C>G (p.Pro152Arg) n.3922C>G c.2999C>G (p.Pro1000Arg) n.4779C>G n.4762C>G | dbSNP |
| 12 | g.45852754C>T | CA384492135 | ARID2 | c.4631C>T (p.Pro1544Leu) c.840C>T c.4552C>T c.4184C>T (p.Pro1395Leu) c.3461C>T (p.Pro1154Leu) c.455C>T (p.Pro152Leu) n.3922C>T c.2999C>T (p.Pro1000Leu) n.4779C>T n.4762C>T | dbSNP |
| 12 | g.45852754_45852774delinsCCAACAATGCTGGCTGCAGCG | CA2033475756 | ARID2 | c.4631_4651delinsCCAACAATGCTGGCTGCAGCG (p.Pro1544=) c.840_860delinsCCAACAATGCTGGCTGCAGCG c.4552_4572delinsCCAACAATGCTGGCTGCAGCG c.4184_4204delinsCCAACAATGCTGGCTGCAGCG (p.Pro1395=) c.3461_3481delinsCCAACAATGCTGGCTGCAGCG (p.Pro1154=) c.455_475delinsCCAACAATGCTGGCTGCAGCG (p.Pro152=) n.3922_3942delinsCCAACAATGCTGGCTGCAGCG c.2999_3019delinsCCAACAATGCTGGCTGCAGCG (p.Pro1000=) n.4779_4799delinsCCAACAATGCTGGCTGCAGCG n.4762_4782delinsCCAACAATGCTGGCTGCAGCG | |
| 12 | g.45852755C>A | CA479694142 | ARID2 | c.4632C>A (p.Pro1544=) c.841C>A c.4553C>A c.4185C>A (p.Pro1395=) c.3462C>A (p.Pro1154=) c.456C>A (p.Pro152=) n.3923C>A c.3000C>A (p.Pro1000=) n.4780C>A n.4763C>A | dbSNP |
| 12 | g.45852755C= | CA2033475757 | ARID2 | c.4632C= (p.Pro1544=) c.841C= c.4553C= c.4185C= (p.Pro1395=) c.3462C= (p.Pro1154=) c.456C= (p.Pro152=) n.3923C= c.3000C= (p.Pro1000=) n.4780C= n.4763C= | |
| 12 | g.45852755C>G | CA479694143 | ARID2 | c.4632C>G (p.Pro1544=) c.841C>G c.4553C>G c.4185C>G (p.Pro1395=) c.3462C>G (p.Pro1154=) c.456C>G (p.Pro152=) n.3923C>G c.3000C>G (p.Pro1000=) n.4780C>G n.4763C>G | dbSNP gnomAD v4 |
| 12 | g.45852755C>T | CA236400888 | ARID2 | c.4632C>T (p.Pro1544=) c.841C>T c.4553C>T c.4185C>T (p.Pro1395=) c.3462C>T (p.Pro1154=) c.456C>T (p.Pro152=) n.3923C>T c.3000C>T (p.Pro1000=) n.4780C>T n.4763C>T | dbSNP gnomAD v4 |
| 12 | g.45852763_45852782del | CA1139662607 | ARID2 | c.4640_4659del (p.Ala1547GlyfsTer14) c.849_868del c.4561_4580del c.4193_4212del (p.Ala1398GlyfsTer14) c.3470_3489del (p.Ala1157GlyfsTer14) c.464_483del (p.Ala155GlyfsTer14) n.3931_3950del c.3008_3027del (p.Ala1003GlyfsTer14) n.4788_4807del n.4771_4790del | ClinVar dbSNP |
| 12 | g.45852756A>C | CA384492136 | ARID2 | c.4633A>C (p.Asn1545His) c.842A>C c.4554A>C c.4186A>C (p.Asn1396His) c.3463A>C (p.Asn1155His) c.457A>C (p.Asn153His) n.3924A>C c.3001A>C (p.Asn1001His) n.4781A>C n.4764A>C | dbSNP |
| 12 | g.45852756A>G | CA384492137 | ARID2 | c.4633A>G (p.Asn1545Asp) c.842A>G c.4554A>G c.4186A>G (p.Asn1396Asp) c.3463A>G (p.Asn1155Asp) c.457A>G (p.Asn153Asp) n.3924A>G c.3001A>G (p.Asn1001Asp) n.4781A>G n.4764A>G | |
| 12 | g.45852756A>T | CA384492138 | ARID2 | c.4633A>T (p.Asn1545Tyr) c.842A>T c.4554A>T c.4186A>T (p.Asn1396Tyr) c.3463A>T (p.Asn1155Tyr) c.457A>T (p.Asn153Tyr) n.3924A>T c.3001A>T (p.Asn1001Tyr) n.4781A>T n.4764A>T | |
| 12 | g.45852757A= | CA2033475758 | ARID2 | c.4634A= (p.Asn1545=) c.843A= c.4555A= c.4187A= (p.Asn1396=) c.3464A= (p.Asn1155=) c.458A= (p.Asn153=) n.3925A= c.3002A= (p.Asn1001=) n.4782A= n.4765A= | |
| 12 | g.45852757A>C | CA384492140 | ARID2 | c.4634A>C (p.Asn1545Thr) c.843A>C c.4555A>C c.4187A>C (p.Asn1396Thr) c.3464A>C (p.Asn1155Thr) c.458A>C (p.Asn153Thr) n.3925A>C c.3002A>C (p.Asn1001Thr) n.4782A>C n.4765A>C | dbSNP |
| 12 | g.45852757A>G | CA6526696 | ARID2 | c.4634A>G (p.Asn1545Ser) c.843A>G c.4555A>G c.4187A>G (p.Asn1396Ser) c.3464A>G (p.Asn1155Ser) c.458A>G (p.Asn153Ser) n.3925A>G c.3002A>G (p.Asn1001Ser) n.4782A>G n.4765A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852757A>T | CA384492139 | ARID2 | c.4634A>T (p.Asn1545Ile) c.843A>T c.4555A>T c.4187A>T (p.Asn1396Ile) c.3464A>T (p.Asn1155Ile) c.458A>T (p.Asn153Ile) n.3925A>T c.3002A>T (p.Asn1001Ile) n.4782A>T n.4765A>T | dbSNP |
| 12 | g.45852758C>A | CA384492141 | ARID2 | c.4635C>A (p.Asn1545Lys) c.844C>A c.4556C>A c.4188C>A (p.Asn1396Lys) c.3465C>A (p.Asn1155Lys) c.459C>A (p.Asn153Lys) n.3926C>A c.3003C>A (p.Asn1001Lys) n.4783C>A n.4766C>A | dbSNP |
| 12 | g.45852758C>G | CA384492142 | ARID2 | c.4635C>G (p.Asn1545Lys) c.844C>G c.4556C>G c.4188C>G (p.Asn1396Lys) c.3465C>G (p.Asn1155Lys) c.459C>G (p.Asn153Lys) n.3926C>G c.3003C>G (p.Asn1001Lys) n.4783C>G n.4766C>G | dbSNP |
| 12 | g.45852758C>T | CA479694144 | ARID2 | c.4635C>T (p.Asn1545=) c.844C>T c.4556C>T c.4188C>T (p.Asn1396=) c.3465C>T (p.Asn1155=) c.459C>T (p.Asn153=) n.3926C>T c.3003C>T (p.Asn1001=) n.4783C>T n.4766C>T | dbSNP |
| 12 | g.45852759A= | CA2033475759 | ARID2 | c.4636A= (p.Asn1546=) c.845A= c.4557A= c.4189A= (p.Asn1397=) c.3466A= (p.Asn1156=) c.460A= (p.Asn154=) n.3927A= c.3004A= (p.Asn1002=) n.4784A= n.4767A= | |
| 12 | g.45852759A>C | CA384492143 | ARID2 | c.4636A>C (p.Asn1546His) c.845A>C c.4557A>C c.4189A>C (p.Asn1397His) c.3466A>C (p.Asn1156His) c.460A>C (p.Asn154His) n.3927A>C c.3004A>C (p.Asn1002His) n.4784A>C n.4767A>C | dbSNP |
| 12 | g.45852759A>G | CA384492144 | ARID2 | c.4636A>G (p.Asn1546Asp) c.845A>G c.4557A>G c.4189A>G (p.Asn1397Asp) c.3466A>G (p.Asn1156Asp) c.460A>G (p.Asn154Asp) n.3927A>G c.3004A>G (p.Asn1002Asp) n.4784A>G n.4767A>G | dbSNP |
| 12 | g.45852759A>T | CA384492145 | ARID2 | c.4636A>T (p.Asn1546Tyr) c.845A>T c.4557A>T c.4189A>T (p.Asn1397Tyr) c.3466A>T (p.Asn1156Tyr) c.460A>T (p.Asn154Tyr) n.3927A>T c.3004A>T (p.Asn1002Tyr) n.4784A>T n.4767A>T | dbSNP |
| 12 | g.45852760A= | CA2033475760 | ARID2 | c.4637A= (p.Asn1546=) c.846A= c.4558A= c.4190A= (p.Asn1397=) c.3467A= (p.Asn1156=) c.461A= (p.Asn154=) n.3928A= c.3005A= (p.Asn1002=) n.4785A= n.4768A= | |
| 12 | g.45852760A>C | CA6526697 | ARID2 | c.4637A>C (p.Asn1546Thr) c.846A>C c.4558A>C c.4190A>C (p.Asn1397Thr) c.3467A>C (p.Asn1156Thr) c.461A>C (p.Asn154Thr) n.3928A>C c.3005A>C (p.Asn1002Thr) n.4785A>C n.4768A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.45852760A>G | CA384492146 | ARID2 | c.4637A>G (p.Asn1546Ser) c.846A>G c.4558A>G c.4190A>G (p.Asn1397Ser) c.3467A>G (p.Asn1156Ser) c.461A>G (p.Asn154Ser) n.3928A>G c.3005A>G (p.Asn1002Ser) n.4785A>G n.4768A>G | dbSNP |
| 12 | g.45852760A>T | CA384492147 | ARID2 | c.4637A>T (p.Asn1546Ile) c.846A>T c.4558A>T c.4190A>T (p.Asn1397Ile) c.3467A>T (p.Asn1156Ile) c.461A>T (p.Asn154Ile) n.3928A>T c.3005A>T (p.Asn1002Ile) n.4785A>T n.4768A>T | dbSNP |
| 12 | g.45852761T>A | CA384492148 | ARID2 | c.4638T>A (p.Asn1546Lys) c.847T>A c.4559T>A c.4191T>A (p.Asn1397Lys) c.3468T>A (p.Asn1156Lys) c.462T>A (p.Asn154Lys) n.3929T>A c.3006T>A (p.Asn1002Lys) n.4786T>A n.4769T>A | dbSNP |
| 12 | g.45852761T>C | CA479694145 | ARID2 | c.4638T>C (p.Asn1546=) c.847T>C c.4559T>C c.4191T>C (p.Asn1397=) c.3468T>C (p.Asn1156=) c.462T>C (p.Asn154=) n.3929T>C c.3006T>C (p.Asn1002=) n.4786T>C n.4769T>C | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852761T>G | CA384492149 | ARID2 | c.4638T>G (p.Asn1546Lys) c.847T>G c.4559T>G c.4191T>G (p.Asn1397Lys) c.3468T>G (p.Asn1156Lys) c.462T>G (p.Asn154Lys) n.3929T>G c.3006T>G (p.Asn1002Lys) n.4786T>G n.4769T>G | dbSNP |
| 12 | g.45852761T= | CA2033475761 | ARID2 | c.4638T= (p.Asn1546=) c.847T= c.4559T= c.4191T= (p.Asn1397=) c.3468T= (p.Asn1156=) c.462T= (p.Asn154=) n.3929T= c.3006T= (p.Asn1002=) n.4786T= n.4769T= | |
| 12 | g.45852762G>A | CA384492150 | ARID2 | c.4639G>A (p.Ala1547Thr) c.848G>A c.4560G>A c.4192G>A (p.Ala1398Thr) c.3469G>A (p.Ala1157Thr) c.463G>A (p.Ala155Thr) n.3930G>A c.3007G>A (p.Ala1003Thr) n.4787G>A n.4770G>A | dbSNP |
| 12 | g.45852762G>C | CA384492151 | ARID2 | c.4639G>C (p.Ala1547Pro) c.848G>C c.4560G>C c.4192G>C (p.Ala1398Pro) c.3469G>C (p.Ala1157Pro) c.463G>C (p.Ala155Pro) n.3930G>C c.3007G>C (p.Ala1003Pro) n.4787G>C n.4770G>C | dbSNP |
| 12 | g.45852762G>T | CA384492152 | ARID2 | c.4639G>T (p.Ala1547Ser) c.848G>T c.4560G>T c.4192G>T (p.Ala1398Ser) c.3469G>T (p.Ala1157Ser) c.463G>T (p.Ala155Ser) n.3930G>T c.3007G>T (p.Ala1003Ser) n.4787G>T n.4770G>T | |
| 12 | g.45852763C>A | CA384492155 | ARID2 | c.4640C>A (p.Ala1547Asp) c.849C>A c.4561C>A c.4193C>A (p.Ala1398Asp) c.3470C>A (p.Ala1157Asp) c.464C>A (p.Ala155Asp) n.3931C>A c.3008C>A (p.Ala1003Asp) n.4788C>A n.4771C>A | dbSNP |
| 12 | g.45852763C= | CA2033475762 | ARID2 | c.4640C= (p.Ala1547=) c.849C= c.4561C= c.4193C= (p.Ala1398=) c.3470C= (p.Ala1157=) c.464C= (p.Ala155=) n.3931C= c.3008C= (p.Ala1003=) n.4788C= n.4771C= | |
| 12 | g.45852763C>G | CA384492153 | ARID2 | c.4640C>G (p.Ala1547Gly) c.849C>G c.4561C>G c.4193C>G (p.Ala1398Gly) c.3470C>G (p.Ala1157Gly) c.464C>G (p.Ala155Gly) n.3931C>G c.3008C>G (p.Ala1003Gly) n.4788C>G n.4771C>G | dbSNP |
| 12 | g.45852763C>T | CA384492154 | ARID2 | c.4640C>T (p.Ala1547Val) c.849C>T c.4561C>T c.4193C>T (p.Ala1398Val) c.3470C>T (p.Ala1157Val) c.464C>T (p.Ala155Val) n.3931C>T c.3008C>T (p.Ala1003Val) n.4788C>T n.4771C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852764T>A | CA479694146 | ARID2 | c.4641T>A (p.Ala1547=) c.850T>A c.4562T>A c.4194T>A (p.Ala1398=) c.3471T>A (p.Ala1157=) c.465T>A (p.Ala155=) n.3932T>A c.3009T>A (p.Ala1003=) n.4789T>A n.4772T>A | |
| 12 | g.45852764T>C | CA479694147 | ARID2 | c.4641T>C (p.Ala1547=) c.850T>C c.4562T>C c.4194T>C (p.Ala1398=) c.3471T>C (p.Ala1157=) c.465T>C (p.Ala155=) n.3932T>C c.3009T>C (p.Ala1003=) n.4789T>C n.4772T>C | |
| 12 | g.45852764T>G | CA479694148 | ARID2 | c.4641T>G (p.Ala1547=) c.850T>G c.4562T>G c.4194T>G (p.Ala1398=) c.3471T>G (p.Ala1157=) c.465T>G (p.Ala155=) n.3932T>G c.3009T>G (p.Ala1003=) n.4789T>G n.4772T>G | |
| 12 | g.45852765G>A | CA384492156 | ARID2 | c.4642G>A (p.Gly1548Ser) c.851G>A c.4563G>A c.4195G>A (p.Gly1399Ser) c.3472G>A (p.Gly1158Ser) c.466G>A (p.Gly156Ser) n.3933G>A c.3010G>A (p.Gly1004Ser) n.4790G>A n.4773G>A | dbSNP |
| 12 | g.45852765G>C | CA384492157 | ARID2 | c.4642G>C (p.Gly1548Arg) c.851G>C c.4563G>C c.4195G>C (p.Gly1399Arg) c.3472G>C (p.Gly1158Arg) c.466G>C (p.Gly156Arg) n.3933G>C c.3010G>C (p.Gly1004Arg) n.4790G>C n.4773G>C | dbSNP |
| 12 | g.45852765G= | CA2033475763 | ARID2 | c.4642G= (p.Gly1548=) c.851G= c.4563G= c.4195G= (p.Gly1399=) c.3472G= (p.Gly1158=) c.466G= (p.Gly156=) n.3933G= c.3010G= (p.Gly1004=) n.4790G= n.4773G= | |
| 12 | g.45852765G>T | CA384492158 | ARID2 | c.4642G>T (p.Gly1548Cys) c.851G>T c.4563G>T c.4195G>T (p.Gly1399Cys) c.3472G>T (p.Gly1158Cys) c.466G>T (p.Gly156Cys) n.3933G>T c.3010G>T (p.Gly1004Cys) n.4790G>T n.4773G>T | |
| 12 | g.45852766G>A | CA384492159 | ARID2 | c.4643G>A (p.Gly1548Asp) c.852G>A c.4564G>A c.4196G>A (p.Gly1399Asp) c.3473G>A (p.Gly1158Asp) c.467G>A (p.Gly156Asp) n.3934G>A c.3011G>A (p.Gly1004Asp) n.4791G>A n.4774G>A | dbSNP |
| 12 | g.45852766G>C | CA384492160 | ARID2 | c.4643G>C (p.Gly1548Ala) c.852G>C c.4564G>C c.4196G>C (p.Gly1399Ala) c.3473G>C (p.Gly1158Ala) c.467G>C (p.Gly156Ala) n.3934G>C c.3011G>C (p.Gly1004Ala) n.4791G>C n.4774G>C | dbSNP |
| 12 | g.45852766G= | CA2033475764 | ARID2 | c.4643G= (p.Gly1548=) c.852G= c.4564G= c.4196G= (p.Gly1399=) c.3473G= (p.Gly1158=) c.467G= (p.Gly156=) n.3934G= c.3011G= (p.Gly1004=) n.4791G= n.4774G= | |
| 12 | g.45852766G>T | CA384492161 | ARID2 | c.4643G>T (p.Gly1548Val) c.852G>T c.4564G>T c.4196G>T (p.Gly1399Val) c.3473G>T (p.Gly1158Val) c.467G>T (p.Gly156Val) n.3934G>T c.3011G>T (p.Gly1004Val) n.4791G>T n.4774G>T | dbSNP |
| 12 | g.45852767C>A | CA479694150 | ARID2 | c.4644C>A (p.Gly1548=) c.853C>A c.4565C>A c.4197C>A (p.Gly1399=) c.3474C>A (p.Gly1158=) c.468C>A (p.Gly156=) n.3935C>A c.3012C>A (p.Gly1004=) n.4792C>A n.4775C>A | dbSNP |
| 12 | g.45852767C= | CA2033475765 | ARID2 | c.4644C= (p.Gly1548=) c.853C= c.4565C= c.4197C= (p.Gly1399=) c.3474C= (p.Gly1158=) c.468C= (p.Gly156=) n.3935C= c.3012C= (p.Gly1004=) n.4792C= n.4775C= | |
| 12 | g.45852767C>G | CA479694152 | ARID2 | c.4644C>G (p.Gly1548=) c.853C>G c.4565C>G c.4197C>G (p.Gly1399=) c.3474C>G (p.Gly1158=) c.468C>G (p.Gly156=) n.3935C>G c.3012C>G (p.Gly1004=) n.4792C>G n.4775C>G | dbSNP |
| 12 | g.45852767C>T | CA479694153 | ARID2 | c.4644C>T (p.Gly1548=) c.853C>T c.4565C>T c.4197C>T (p.Gly1399=) c.3474C>T (p.Gly1158=) c.468C>T (p.Gly156=) n.3935C>T c.3012C>T (p.Gly1004=) n.4792C>T n.4775C>T | dbSNP gnomAD v4 COSMIC |
| 12 | g.45852768T>A | CA384492162 | ARID2 | c.4645T>A (p.Cys1549Ser) c.854T>A c.4566T>A c.4198T>A (p.Cys1400Ser) c.3475T>A (p.Cys1159Ser) c.469T>A (p.Cys157Ser) n.3936T>A c.3013T>A (p.Cys1005Ser) n.4793T>A n.4776T>A | dbSNP |
| 12 | g.45852768T>C | CA384492163 | ARID2 | c.4645T>C (p.Cys1549Arg) c.854T>C c.4566T>C c.4198T>C (p.Cys1400Arg) c.3475T>C (p.Cys1159Arg) c.469T>C (p.Cys157Arg) n.3936T>C c.3013T>C (p.Cys1005Arg) n.4793T>C n.4776T>C | dbSNP |
| 12 | g.45852768T>G | CA384492164 | ARID2 | c.4645T>G (p.Cys1549Gly) c.854T>G c.4566T>G c.4198T>G (p.Cys1400Gly) c.3475T>G (p.Cys1159Gly) c.469T>G (p.Cys157Gly) n.3936T>G c.3013T>G (p.Cys1005Gly) n.4793T>G n.4776T>G | |
| 12 | g.45852769G>A | CA384492165 | ARID2 | c.4646G>A (p.Cys1549Tyr) c.855G>A c.4567G>A c.4199G>A (p.Cys1400Tyr) c.3476G>A (p.Cys1159Tyr) c.470G>A (p.Cys157Tyr) n.3937G>A c.3014G>A (p.Cys1005Tyr) n.4794G>A n.4777G>A | dbSNP gnomAD v4 |
| 12 | g.45852769G>C | CA384492166 | ARID2 | c.4646G>C (p.Cys1549Ser) c.855G>C c.4567G>C c.4199G>C (p.Cys1400Ser) c.3476G>C (p.Cys1159Ser) c.470G>C (p.Cys157Ser) n.3937G>C c.3014G>C (p.Cys1005Ser) n.4794G>C n.4777G>C | dbSNP |
| 12 | g.45852769G>T | CA384492167 | ARID2 | c.4646G>T (p.Cys1549Phe) c.855G>T c.4567G>T c.4199G>T (p.Cys1400Phe) c.3476G>T (p.Cys1159Phe) c.470G>T (p.Cys157Phe) n.3937G>T c.3014G>T (p.Cys1005Phe) n.4794G>T n.4777G>T | dbSNP gnomAD v4 |
| 12 | g.45852770C>A | CA384492168 | ARID2 | c.4647C>A (p.Cys1549Ter) c.856C>A c.4568C>A c.4200C>A (p.Cys1400Ter) c.3477C>A (p.Cys1159Ter) c.471C>A (p.Cys157Ter) n.3938C>A c.3015C>A (p.Cys1005Ter) n.4795C>A n.4778C>A | dbSNP |
| 12 | g.45852770C>G | CA384492169 | ARID2 | c.4647C>G (p.Cys1549Trp) c.856C>G c.4568C>G c.4200C>G (p.Cys1400Trp) c.3477C>G (p.Cys1159Trp) c.471C>G (p.Cys157Trp) n.3938C>G c.3015C>G (p.Cys1005Trp) n.4795C>G n.4778C>G | dbSNP |
| 12 | g.45852770C>T | CA479694157 | ARID2 | c.4647C>T (p.Cys1549=) c.856C>T c.4568C>T c.4200C>T (p.Cys1400=) c.3477C>T (p.Cys1159=) c.471C>T (p.Cys157=) n.3938C>T c.3015C>T (p.Cys1005=) n.4795C>T n.4778C>T | dbSNP gnomAD v4 |
| 12 | g.45852771A= | CA2033475766 | ARID2 | c.4648A= (p.Ser1550=) c.857A= c.4569A= c.4201A= (p.Ser1401=) c.3478A= (p.Ser1160=) c.472A= (p.Ser158=) n.3939A= c.3016A= (p.Ser1006=) n.4796A= n.4779A= | |
| 12 | g.45852771A>C | CA384492170 | ARID2 | c.4648A>C (p.Ser1550Arg) c.857A>C c.4569A>C c.4201A>C (p.Ser1401Arg) c.3478A>C (p.Ser1160Arg) c.472A>C (p.Ser158Arg) n.3939A>C c.3016A>C (p.Ser1006Arg) n.4796A>C n.4779A>C | |
| 12 | g.45852771A>G | CA236400916 | ARID2 | c.4648A>G (p.Ser1550Gly) c.857A>G c.4569A>G c.4201A>G (p.Ser1401Gly) c.3478A>G (p.Ser1160Gly) c.472A>G (p.Ser158Gly) n.3939A>G c.3016A>G (p.Ser1006Gly) n.4796A>G n.4779A>G | dbSNP gnomAD v4 |
| 12 | g.45852771A>T | CA384492171 | ARID2 | c.4648A>T (p.Ser1550Cys) c.857A>T c.4569A>T c.4201A>T (p.Ser1401Cys) c.3478A>T (p.Ser1160Cys) c.472A>T (p.Ser158Cys) n.3939A>T c.3016A>T (p.Ser1006Cys) n.4796A>T n.4779A>T | dbSNP |
| 12 | g.45852772G>A | CA384492172 | ARID2 | c.4649G>A (p.Ser1550Asn) c.858G>A c.4570G>A c.4202G>A (p.Ser1401Asn) c.3479G>A (p.Ser1160Asn) c.473G>A (p.Ser158Asn) n.3940G>A c.3017G>A (p.Ser1006Asn) n.4797G>A n.4780G>A | dbSNP |
| 12 | g.45852772G>C | CA384492173 | ARID2 | c.4649G>C (p.Ser1550Thr) c.858G>C c.4570G>C c.4202G>C (p.Ser1401Thr) c.3479G>C (p.Ser1160Thr) c.473G>C (p.Ser158Thr) n.3940G>C c.3017G>C (p.Ser1006Thr) n.4797G>C n.4780G>C | dbSNP |
| 12 | g.45852772G>T | CA384492174 | ARID2 | c.4649G>T (p.Ser1550Ile) c.858G>T c.4570G>T c.4202G>T (p.Ser1401Ile) c.3479G>T (p.Ser1160Ile) c.473G>T (p.Ser158Ile) n.3940G>T c.3017G>T (p.Ser1006Ile) n.4797G>T n.4780G>T | |
| 12 | g.45852773C>A | CA384492176 | ARID2 | c.4650C>A (p.Ser1550Arg) c.859C>A c.4571C>A c.4203C>A (p.Ser1401Arg) c.3480C>A (p.Ser1160Arg) c.474C>A (p.Ser158Arg) n.3941C>A c.3018C>A (p.Ser1006Arg) n.4798C>A n.4781C>A | dbSNP |
| 12 | g.45852773C= | CA2033475767 | ARID2 | c.4650C= (p.Ser1550=) c.859C= c.4571C= c.4203C= (p.Ser1401=) c.3480C= (p.Ser1160=) c.474C= (p.Ser158=) n.3941C= c.3018C= (p.Ser1006=) n.4798C= n.4781C= | |
| 12 | g.45852773C>G | CA384492175 | ARID2 | c.4650C>G (p.Ser1550Arg) c.859C>G c.4571C>G c.4203C>G (p.Ser1401Arg) c.3480C>G (p.Ser1160Arg) c.474C>G (p.Ser158Arg) n.3941C>G c.3018C>G (p.Ser1006Arg) n.4798C>G n.4781C>G | dbSNP |
| 12 | g.45852773C>T | CA6526698 | ARID2 | c.4650C>T (p.Ser1550=) c.859C>T c.4571C>T c.4203C>T (p.Ser1401=) c.3480C>T (p.Ser1160=) c.474C>T (p.Ser158=) n.3941C>T c.3018C>T (p.Ser1006=) n.4798C>T n.4781C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852774G>A | CA384492177 | ARID2 | c.4651G>A (p.Ala1551Thr) c.860G>A c.4572G>A c.4204G>A (p.Ala1402Thr) c.3481G>A (p.Ala1161Thr) c.475G>A (p.Ala159Thr) n.3942G>A c.3019G>A (p.Ala1007Thr) n.4799G>A n.4782G>A | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 12 | g.45852774G>C | CA384492178 | ARID2 | c.4651G>C (p.Ala1551Pro) c.860G>C c.4572G>C c.4204G>C (p.Ala1402Pro) c.3481G>C (p.Ala1161Pro) c.475G>C (p.Ala159Pro) n.3942G>C c.3019G>C (p.Ala1007Pro) n.4799G>C n.4782G>C | dbSNP |
| 12 | g.45852774G= | CA2033475768 | ARID2 | c.4651G= (p.Ala1551=) c.860G= c.4572G= c.4204G= (p.Ala1402=) c.3481G= (p.Ala1161=) c.475G= (p.Ala159=) n.3942G= c.3019G= (p.Ala1007=) n.4799G= n.4782G= | |
| 12 | g.45852774G>T | CA384492179 | ARID2 | c.4651G>T (p.Ala1551Ser) c.860G>T c.4572G>T c.4204G>T (p.Ala1402Ser) c.3481G>T (p.Ala1161Ser) c.475G>T (p.Ala159Ser) n.3942G>T c.3019G>T (p.Ala1007Ser) n.4799G>T n.4782G>T | gnomAD v4 |
| 12 | g.45852775C>A | CA384492180 | ARID2 | c.4652C>A (p.Ala1551Glu) c.861C>A c.4573C>A c.4205C>A (p.Ala1402Glu) c.3482C>A (p.Ala1161Glu) c.476C>A (p.Ala159Glu) n.3943C>A c.3020C>A (p.Ala1007Glu) n.4800C>A n.4783C>A | dbSNP |
| 12 | g.45852775C= | CA2033475769 | ARID2 | c.4652C= (p.Ala1551=) c.861C= c.4573C= c.4205C= (p.Ala1402=) c.3482C= (p.Ala1161=) c.476C= (p.Ala159=) n.3943C= c.3020C= (p.Ala1007=) n.4800C= n.4783C= | |
| 12 | g.45852775C>G | CA384492181 | ARID2 | c.4652C>G (p.Ala1551Gly) c.861C>G c.4573C>G c.4205C>G (p.Ala1402Gly) c.3482C>G (p.Ala1161Gly) c.476C>G (p.Ala159Gly) n.3943C>G c.3020C>G (p.Ala1007Gly) n.4800C>G n.4783C>G | dbSNP |
| 12 | g.45852775C>T | CA236400922 | ARID2 | c.4652C>T (p.Ala1551Val) c.861C>T c.4573C>T c.4205C>T (p.Ala1402Val) c.3482C>T (p.Ala1161Val) c.476C>T (p.Ala159Val) n.3943C>T c.3020C>T (p.Ala1007Val) n.4800C>T n.4783C>T | dbSNP |
| 12 | g.45852776A>C | CA479694160 | ARID2 | c.4653A>C (p.Ala1551=) c.862A>C c.4574A>C c.4206A>C (p.Ala1402=) c.3483A>C (p.Ala1161=) c.477A>C (p.Ala159=) n.3944A>C c.3021A>C (p.Ala1007=) n.4801A>C n.4784A>C | |
| 12 | g.45852776A>G | CA479694161 | ARID2 | c.4653A>G (p.Ala1551=) c.862A>G c.4574A>G c.4206A>G (p.Ala1402=) c.3483A>G (p.Ala1161=) c.477A>G (p.Ala159=) n.3944A>G c.3021A>G (p.Ala1007=) n.4801A>G n.4784A>G | |
| 12 | g.45852776A>T | CA479694162 | ARID2 | c.4653A>T (p.Ala1551=) c.862A>T c.4574A>T c.4206A>T (p.Ala1402=) c.3483A>T (p.Ala1161=) c.477A>T (p.Ala159=) n.3944A>T c.3021A>T (p.Ala1007=) n.4801A>T n.4784A>T | dbSNP |
| 12 | g.45852777A= | CA2033475770 | ARID2 | c.4654A= (p.Thr1552=) c.863A= c.4575A= c.4207A= (p.Thr1403=) c.3484A= (p.Thr1162=) c.478A= (p.Thr160=) n.3945A= c.3022A= (p.Thr1008=) n.4802A= n.4785A= | |
| 12 | g.45852777A>C | CA384492182 | ARID2 | c.4654A>C (p.Thr1552Pro) c.863A>C c.4575A>C c.4207A>C (p.Thr1403Pro) c.3484A>C (p.Thr1162Pro) c.478A>C (p.Thr160Pro) n.3945A>C c.3022A>C (p.Thr1008Pro) n.4802A>C n.4785A>C | dbSNP |
| 12 | g.45852777A>G | CA384492184 | ARID2 | c.4654A>G (p.Thr1552Ala) c.863A>G c.4575A>G c.4207A>G (p.Thr1403Ala) c.3484A>G (p.Thr1162Ala) c.478A>G (p.Thr160Ala) n.3945A>G c.3022A>G (p.Thr1008Ala) n.4802A>G n.4785A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852777A>T | CA384492183 | ARID2 | c.4654A>T (p.Thr1552Ser) c.863A>T c.4575A>T c.4207A>T (p.Thr1403Ser) c.3484A>T (p.Thr1162Ser) c.478A>T (p.Thr160Ser) n.3945A>T c.3022A>T (p.Thr1008Ser) n.4802A>T n.4785A>T | dbSNP |
| 12 | g.45852778C>A | CA384492185 | ARID2 | c.4655C>A (p.Thr1552Lys) c.864C>A c.4576C>A c.4208C>A (p.Thr1403Lys) c.3485C>A (p.Thr1162Lys) c.479C>A (p.Thr160Lys) n.3946C>A c.3023C>A (p.Thr1008Lys) n.4803C>A n.4786C>A | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852778C= | CA2033475771 | ARID2 | c.4655C= (p.Thr1552=) c.864C= c.4576C= c.4208C= (p.Thr1403=) c.3485C= (p.Thr1162=) c.479C= (p.Thr160=) n.3946C= c.3023C= (p.Thr1008=) n.4803C= n.4786C= | |
| 12 | g.45852778C>G | CA6526699 | ARID2 | c.4655C>G (p.Thr1552Arg) c.864C>G c.4576C>G c.4208C>G (p.Thr1403Arg) c.3485C>G (p.Thr1162Arg) c.479C>G (p.Thr160Arg) n.3946C>G c.3023C>G (p.Thr1008Arg) n.4803C>G n.4786C>G | dbSNP ExAC gnomAD v2 |
| 12 | g.45852778C>T | CA384492186 | ARID2 | c.4655C>T (p.Thr1552Ile) c.864C>T c.4576C>T c.4208C>T (p.Thr1403Ile) c.3485C>T (p.Thr1162Ile) c.479C>T (p.Thr160Ile) n.3946C>T c.3023C>T (p.Thr1008Ile) n.4803C>T n.4786C>T | dbSNP |
| 12 | g.45852779A>C | CA479694166 | ARID2 | c.4656A>C (p.Thr1552=) c.865A>C c.4577A>C c.4209A>C (p.Thr1403=) c.3486A>C (p.Thr1162=) c.480A>C (p.Thr160=) n.3947A>C c.3024A>C (p.Thr1008=) n.4804A>C n.4787A>C | |
| 12 | g.45852779A>G | CA479694167 | ARID2 | c.4656A>G (p.Thr1552=) c.865A>G c.4577A>G c.4209A>G (p.Thr1403=) c.3486A>G (p.Thr1162=) c.480A>G (p.Thr160=) n.3947A>G c.3024A>G (p.Thr1008=) n.4804A>G n.4787A>G | gnomAD v4 |
| 12 | g.45852779A>T | CA479694168 | ARID2 | c.4656A>T (p.Thr1552=) c.865A>T c.4577A>T c.4209A>T (p.Thr1403=) c.3486A>T (p.Thr1162=) c.480A>T (p.Thr160=) n.3947A>T c.3024A>T (p.Thr1008=) n.4804A>T n.4787A>T | dbSNP |
| 12 | g.45852780A>C | CA384492187 | ARID2 | c.4657A>C (p.Met1553Leu) c.866A>C c.4578A>C c.4210A>C (p.Met1404Leu) c.3487A>C (p.Met1163Leu) c.481A>C (p.Met161Leu) n.3948A>C c.3025A>C (p.Met1009Leu) n.4805A>C n.4788A>C | |
| 12 | g.45852780A>G | CA384492188 | ARID2 | c.4657A>G (p.Met1553Val) c.866A>G c.4578A>G c.4210A>G (p.Met1404Val) c.3487A>G (p.Met1163Val) c.481A>G (p.Met161Val) n.3948A>G c.3025A>G (p.Met1009Val) n.4805A>G n.4788A>G | dbSNP gnomAD v4 |
| 12 | g.45852780A>T | CA384492189 | ARID2 | c.4657A>T (p.Met1553Leu) c.866A>T c.4578A>T c.4210A>T (p.Met1404Leu) c.3487A>T (p.Met1163Leu) c.481A>T (p.Met161Leu) n.3948A>T c.3025A>T (p.Met1009Leu) n.4805A>T n.4788A>T | dbSNP |
| 12 | g.45852781T>A | CA384492190 | ARID2 | c.4658T>A (p.Met1553Lys) c.867T>A c.4579T>A c.4211T>A (p.Met1404Lys) c.3488T>A (p.Met1163Lys) c.482T>A (p.Met161Lys) n.3949T>A c.3026T>A (p.Met1009Lys) n.4806T>A n.4789T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852781T>C | CA384492191 | ARID2 | c.4658T>C (p.Met1553Thr) c.867T>C c.4579T>C c.4211T>C (p.Met1404Thr) c.3488T>C (p.Met1163Thr) c.482T>C (p.Met161Thr) n.3949T>C c.3026T>C (p.Met1009Thr) n.4806T>C n.4789T>C | |
| 12 | g.45852781T>G | CA384492192 | ARID2 | c.4658T>G (p.Met1553Arg) c.867T>G c.4579T>G c.4211T>G (p.Met1404Arg) c.3488T>G (p.Met1163Arg) c.482T>G (p.Met161Arg) n.3949T>G c.3026T>G (p.Met1009Arg) n.4806T>G n.4789T>G | |
| 12 | g.45852781T= | CA2033475772 | ARID2 | c.4658T= (p.Met1553=) c.867T= c.4579T= c.4211T= (p.Met1404=) c.3488T= (p.Met1163=) c.482T= (p.Met161=) n.3949T= c.3026T= (p.Met1009=) n.4806T= n.4789T= | |
| 12 | g.45852782G>A | CA384492193 | ARID2 | c.4659G>A (p.Met1553Ile) c.868G>A c.4580G>A c.4212G>A (p.Met1404Ile) c.3489G>A (p.Met1163Ile) c.483G>A (p.Met161Ile) n.3950G>A c.3027G>A (p.Met1009Ile) n.4807G>A n.4790G>A | dbSNP |
| 12 | g.45852782G>C | CA384492194 | ARID2 | c.4659G>C (p.Met1553Ile) c.868G>C c.4580G>C c.4212G>C (p.Met1404Ile) c.3489G>C (p.Met1163Ile) c.483G>C (p.Met161Ile) n.3950G>C c.3027G>C (p.Met1009Ile) n.4807G>C n.4790G>C | dbSNP |
| 12 | g.45852782G>T | CA384492195 | ARID2 | c.4659G>T (p.Met1553Ile) c.868G>T c.4580G>T c.4212G>T (p.Met1404Ile) c.3489G>T (p.Met1163Ile) c.483G>T (p.Met161Ile) n.3950G>T c.3027G>T (p.Met1009Ile) n.4807G>T n.4790G>T | |
| 12 | g.45852783G>A | CA384492196 | ARID2 | c.4660G>A (p.Val1554Ile) c.869G>A c.4581G>A c.4213G>A (p.Val1405Ile) c.3490G>A (p.Val1164Ile) c.484G>A (p.Val162Ile) n.3951G>A c.3028G>A (p.Val1010Ile) n.4808G>A n.4791G>A | dbSNP |
| 12 | g.45852783G>C | CA384492198 | ARID2 | c.4660G>C (p.Val1554Leu) c.869G>C c.4581G>C c.4213G>C (p.Val1405Leu) c.3490G>C (p.Val1164Leu) c.484G>C (p.Val162Leu) n.3951G>C c.3028G>C (p.Val1010Leu) n.4808G>C n.4791G>C | dbSNP |
| 12 | g.45852783G>T | CA384492197 | ARID2 | c.4660G>T (p.Val1554Phe) c.869G>T c.4581G>T c.4213G>T (p.Val1405Phe) c.3490G>T (p.Val1164Phe) c.484G>T (p.Val162Phe) n.3951G>T c.3028G>T (p.Val1010Phe) n.4808G>T n.4791G>T | |
| 12 | g.45852784T>A | CA384492199 | ARID2 | c.4661T>A (p.Val1554Asp) c.870T>A c.4582T>A c.4214T>A (p.Val1405Asp) c.3491T>A (p.Val1164Asp) c.485T>A (p.Val162Asp) n.3952T>A c.3029T>A (p.Val1010Asp) n.4809T>A n.4792T>A | dbSNP |
| 12 | g.45852784T>C | CA384492200 | ARID2 | c.4661T>C (p.Val1554Ala) c.870T>C c.4582T>C c.4214T>C (p.Val1405Ala) c.3491T>C (p.Val1164Ala) c.485T>C (p.Val162Ala) n.3952T>C c.3029T>C (p.Val1010Ala) n.4809T>C n.4792T>C | dbSNP |
| 12 | g.45852784T>G | CA384492201 | ARID2 | c.4661T>G (p.Val1554Gly) c.870T>G c.4582T>G c.4214T>G (p.Val1405Gly) c.3491T>G (p.Val1164Gly) c.485T>G (p.Val162Gly) n.3952T>G c.3029T>G (p.Val1010Gly) n.4809T>G n.4792T>G | dbSNP |
| 12 | g.45852785T>A | CA479694173 | ARID2 | c.4662T>A (p.Val1554=) c.871T>A c.4583T>A c.4215T>A (p.Val1405=) c.3492T>A (p.Val1164=) c.486T>A (p.Val162=) n.3953T>A c.3030T>A (p.Val1010=) n.4810T>A n.4793T>A | |
| 12 | g.45852785T>C | CA479694174 | ARID2 | c.4662T>C (p.Val1554=) c.871T>C c.4583T>C c.4215T>C (p.Val1405=) c.3492T>C (p.Val1164=) c.486T>C (p.Val162=) n.3953T>C c.3030T>C (p.Val1010=) n.4810T>C n.4793T>C | |
| 12 | g.45852785T>G | CA479694175 | ARID2 | c.4662T>G (p.Val1554=) c.871T>G c.4583T>G c.4215T>G (p.Val1405=) c.3492T>G (p.Val1164=) c.486T>G (p.Val162=) n.3953T>G c.3030T>G (p.Val1010=) n.4810T>G n.4793T>G | dbSNP |
| 12 | g.45852786G>A | CA384492202 | ARID2 | c.4663G>A (p.Ala1555Thr) c.872G>A c.4584G>A c.4216G>A (p.Ala1406Thr) c.3493G>A (p.Ala1165Thr) c.487G>A (p.Ala163Thr) n.3954G>A c.3031G>A (p.Ala1011Thr) n.4811G>A n.4794G>A | dbSNP |
| 12 | g.45852786G>C | CA384492203 | ARID2 | c.4663G>C (p.Ala1555Pro) c.872G>C c.4584G>C c.4216G>C (p.Ala1406Pro) c.3493G>C (p.Ala1165Pro) c.487G>C (p.Ala163Pro) n.3954G>C c.3031G>C (p.Ala1011Pro) n.4811G>C n.4794G>C | dbSNP |
| 12 | g.45852786G= | CA2033475773 | ARID2 | c.4663G= (p.Ala1555=) c.872G= c.4584G= c.4216G= (p.Ala1406=) c.3493G= (p.Ala1165=) c.487G= (p.Ala163=) n.3954G= c.3031G= (p.Ala1011=) n.4811G= n.4794G= | |
| 12 | g.45852786G>T | CA6526700 | ARID2 | c.4663G>T (p.Ala1555Ser) c.872G>T c.4584G>T c.4216G>T (p.Ala1406Ser) c.3493G>T (p.Ala1165Ser) c.487G>T (p.Ala163Ser) n.3954G>T c.3031G>T (p.Ala1011Ser) n.4811G>T n.4794G>T | dbSNP ExAC gnomAD v4 COSMIC |
| 12 | g.45852787C>A | CA384492204 | ARID2 | c.4664C>A (p.Ala1555Asp) c.873C>A c.4585C>A c.4217C>A (p.Ala1406Asp) c.3494C>A (p.Ala1165Asp) c.488C>A (p.Ala163Asp) n.3955C>A c.3032C>A (p.Ala1011Asp) n.4812C>A n.4795C>A | dbSNP |
| 12 | g.45852787C>G | CA384492205 | ARID2 | c.4664C>G (p.Ala1555Gly) c.873C>G c.4585C>G c.4217C>G (p.Ala1406Gly) c.3494C>G (p.Ala1165Gly) c.488C>G (p.Ala163Gly) n.3955C>G c.3032C>G (p.Ala1011Gly) n.4812C>G n.4795C>G | dbSNP |
| 12 | g.45852787C>T | CA384492206 | ARID2 | c.4664C>T (p.Ala1555Val) c.873C>T c.4585C>T c.4217C>T (p.Ala1406Val) c.3494C>T (p.Ala1165Val) c.488C>T (p.Ala163Val) n.3955C>T c.3032C>T (p.Ala1011Val) n.4812C>T n.4795C>T | dbSNP |
| 12 | g.45852788T>A | CA479694179 | ARID2 | c.4665T>A (p.Ala1555=) c.874T>A c.4586T>A c.4218T>A (p.Ala1406=) c.3495T>A (p.Ala1165=) c.489T>A (p.Ala163=) n.3956T>A c.3033T>A (p.Ala1011=) n.4813T>A n.4796T>A | dbSNP |
| 12 | g.45852788T>C | CA6526701 | ARID2 | c.4665T>C (p.Ala1555=) c.874T>C c.4586T>C c.4218T>C (p.Ala1406=) c.3495T>C (p.Ala1165=) c.489T>C (p.Ala163=) n.3956T>C c.3033T>C (p.Ala1011=) n.4813T>C n.4796T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.45852788T>G | CA479694177 | ARID2 | c.4665T>G (p.Ala1555=) c.874T>G c.4586T>G c.4218T>G (p.Ala1406=) c.3495T>G (p.Ala1165=) c.489T>G (p.Ala163=) n.3956T>G c.3033T>G (p.Ala1011=) n.4813T>G n.4796T>G | |
| 12 | g.45852788T= | CA2033475774 | ARID2 | c.4665T= (p.Ala1555=) c.874T= c.4586T= c.4218T= (p.Ala1406=) c.3495T= (p.Ala1165=) c.489T= (p.Ala163=) n.3956T= c.3033T= (p.Ala1011=) n.4813T= n.4796T= | |
| 12 | g.45852789G>A | CA384492207 | ARID2 | c.4666G>A (p.Val1556Met) c.875G>A c.4587G>A c.4219G>A (p.Val1407Met) c.3496G>A (p.Val1166Met) c.490G>A (p.Val164Met) n.3957G>A c.3034G>A (p.Val1012Met) n.4814G>A n.4797G>A | dbSNP |
| 12 | g.45852789G>C | CA384492208 | ARID2 | c.4666G>C (p.Val1556Leu) c.875G>C c.4587G>C c.4219G>C (p.Val1407Leu) c.3496G>C (p.Val1166Leu) c.490G>C (p.Val164Leu) n.3957G>C c.3034G>C (p.Val1012Leu) n.4814G>C n.4797G>C | dbSNP |
| 12 | g.45852789G= | CA2033475775 | ARID2 | c.4666G= (p.Val1556=) c.875G= c.4587G= c.4219G= (p.Val1407=) c.3496G= (p.Val1166=) c.490G= (p.Val164=) n.3957G= c.3034G= (p.Val1012=) n.4814G= n.4797G= | |
| 12 | g.45852789G>T | CA384492209 | ARID2 | c.4666G>T (p.Val1556Leu) c.875G>T c.4587G>T c.4219G>T (p.Val1407Leu) c.3496G>T (p.Val1166Leu) c.490G>T (p.Val164Leu) n.3957G>T c.3034G>T (p.Val1012Leu) n.4814G>T n.4797G>T | dbSNP gnomAD v2 |
| 12 | g.45852790T>A | CA384492215 | ARID2 | c.4667T>A (p.Val1556Glu) c.876T>A c.4588T>A c.4220T>A (p.Val1407Glu) c.3497T>A (p.Val1166Glu) c.491T>A (p.Val164Glu) n.3958T>A c.3035T>A (p.Val1012Glu) n.4815T>A n.4798T>A | dbSNP |
| 12 | g.45852790T>C | CA384492212 | ARID2 | c.4667T>C (p.Val1556Ala) c.876T>C c.4588T>C c.4220T>C (p.Val1407Ala) c.3497T>C (p.Val1166Ala) c.491T>C (p.Val164Ala) n.3958T>C c.3035T>C (p.Val1012Ala) n.4815T>C n.4798T>C | |
| 12 | g.45852790T>G | CA384492214 | ARID2 | c.4667T>G (p.Val1556Gly) c.876T>G c.4588T>G c.4220T>G (p.Val1407Gly) c.3497T>G (p.Val1166Gly) c.491T>G (p.Val164Gly) n.3958T>G c.3035T>G (p.Val1012Gly) n.4815T>G n.4798T>G | dbSNP |
| 12 | g.45852791G>A | CA479694180 | ARID2 | c.4668G>A (p.Val1556=) c.877G>A c.4589G>A c.4221G>A (p.Val1407=) c.3498G>A (p.Val1166=) c.492G>A (p.Val164=) n.3959G>A c.3036G>A (p.Val1012=) n.4816G>A n.4799G>A | gnomAD v4 |
| 12 | g.45852791G>C | CA479694181 | ARID2 | c.4668G>C (p.Val1556=) c.877G>C c.4589G>C c.4221G>C (p.Val1407=) c.3498G>C (p.Val1166=) c.492G>C (p.Val164=) n.3959G>C c.3036G>C (p.Val1012=) n.4816G>C n.4799G>C | |
| 12 | g.45852791G= | CA2033475776 | ARID2 | c.4668G= (p.Val1556=) c.877G= c.4589G= c.4221G= (p.Val1407=) c.3498G= (p.Val1166=) c.492G= (p.Val164=) n.3959G= c.3036G= (p.Val1012=) n.4816G= n.4799G= | |
| 12 | g.45852791G>T | CA479694182 | ARID2 | c.4668G>T (p.Val1556=) c.877G>T c.4589G>T c.4221G>T (p.Val1407=) c.3498G>T (p.Val1166=) c.492G>T (p.Val164=) n.3959G>T c.3036G>T (p.Val1012=) n.4816G>T n.4799G>T | dbSNP |
| 12 | g.45852792C>A | CA384492219 | ARID2 | c.4669C>A (p.Pro1557Thr) c.878C>A c.4590C>A c.4222C>A (p.Pro1408Thr) c.3499C>A (p.Pro1167Thr) c.493C>A (p.Pro165Thr) n.3960C>A c.3037C>A (p.Pro1013Thr) n.4817C>A n.4800C>A | dbSNP |
| 12 | g.45852792C>G | CA384492220 | ARID2 | c.4669C>G (p.Pro1557Ala) c.878C>G c.4590C>G c.4222C>G (p.Pro1408Ala) c.3499C>G (p.Pro1167Ala) c.493C>G (p.Pro165Ala) n.3960C>G c.3037C>G (p.Pro1013Ala) n.4817C>G n.4800C>G | dbSNP |
| 12 | g.45852792C>T | CA384492222 | ARID2 | c.4669C>T (p.Pro1557Ser) c.878C>T c.4590C>T c.4222C>T (p.Pro1408Ser) c.3499C>T (p.Pro1167Ser) c.493C>T (p.Pro165Ser) n.3960C>T c.3037C>T (p.Pro1013Ser) n.4817C>T n.4800C>T | dbSNP |
| 12 | g.45852793C>A | CA384492227 | ARID2 | c.4670C>A (p.Pro1557Gln) c.879C>A c.4591C>A c.4223C>A (p.Pro1408Gln) c.3500C>A (p.Pro1167Gln) c.494C>A (p.Pro165Gln) n.3961C>A c.3038C>A (p.Pro1013Gln) n.4818C>A n.4801C>A | |
| 12 | g.45852793C= | CA2033475777 | ARID2 | c.4670C= (p.Pro1557=) c.879C= c.4591C= c.4223C= (p.Pro1408=) c.3500C= (p.Pro1167=) c.494C= (p.Pro165=) n.3961C= c.3038C= (p.Pro1013=) n.4818C= n.4801C= | |
| 12 | g.45852793C>G | CA384492228 | ARID2 | c.4670C>G (p.Pro1557Arg) c.879C>G c.4591C>G c.4223C>G (p.Pro1408Arg) c.3500C>G (p.Pro1167Arg) c.494C>G (p.Pro165Arg) n.3961C>G c.3038C>G (p.Pro1013Arg) n.4818C>G n.4801C>G | |
| 12 | g.45852793C>T | CA384492230 | ARID2 | c.4670C>T (p.Pro1557Leu) c.879C>T c.4591C>T c.4223C>T (p.Pro1408Leu) c.3500C>T (p.Pro1167Leu) c.494C>T (p.Pro165Leu) n.3961C>T c.3038C>T (p.Pro1013Leu) n.4818C>T n.4801C>T | dbSNP |