| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 |
| 12 | g.45852794A= | CA2033475778 | ARID2 | c.4671A= (p.Pro1557=) c.880A= c.4592A= c.4224A= (p.Pro1408=) c.3501A= (p.Pro1167=) c.495A= (p.Pro165=) n.3962A= c.3039A= (p.Pro1013=) n.4819A= n.4802A= | |
| 12 | g.45852794A>C | CA479694184 | ARID2 | c.4671A>C (p.Pro1557=) c.880A>C c.4592A>C c.4224A>C (p.Pro1408=) c.3501A>C (p.Pro1167=) c.495A>C (p.Pro165=) n.3962A>C c.3039A>C (p.Pro1013=) n.4819A>C n.4802A>C | |
| 12 | g.45852794A>G | CA6526703 | ARID2 | c.4671A>G (p.Pro1557=) c.880A>G c.4592A>G c.4224A>G (p.Pro1408=) c.3501A>G (p.Pro1167=) c.495A>G (p.Pro165=) n.3962A>G c.3039A>G (p.Pro1013=) n.4819A>G n.4802A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852794A>T | CA6526702 | ARID2 | c.4671A>T (p.Pro1557=) c.880A>T c.4592A>T c.4224A>T (p.Pro1408=) c.3501A>T (p.Pro1167=) c.495A>T (p.Pro165=) n.3962A>T c.3039A>T (p.Pro1013=) n.4819A>T n.4802A>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852795G>A | CA384492238 | ARID2 | c.4672G>A (p.Ala1558Thr) c.881G>A c.4593G>A c.4225G>A (p.Ala1409Thr) c.3502G>A (p.Ala1168Thr) c.496G>A (p.Ala166Thr) n.3963G>A c.3040G>A (p.Ala1014Thr) n.4820G>A n.4803G>A | dbSNP |
| 12 | g.45852795G>C | CA384492239 | ARID2 | c.4672G>C (p.Ala1558Pro) c.881G>C c.4593G>C c.4225G>C (p.Ala1409Pro) c.3502G>C (p.Ala1168Pro) c.496G>C (p.Ala166Pro) n.3963G>C c.3040G>C (p.Ala1014Pro) n.4820G>C n.4803G>C | dbSNP |
| 12 | g.45852795G>T | CA384492242 | ARID2 | c.4672G>T (p.Ala1558Ser) c.881G>T c.4593G>T c.4225G>T (p.Ala1409Ser) c.3502G>T (p.Ala1168Ser) c.496G>T (p.Ala166Ser) n.3963G>T c.3040G>T (p.Ala1014Ser) n.4820G>T n.4803G>T | dbSNP |
| 12 | g.45852796C>A | CA384492244 | ARID2 | c.4673C>A (p.Ala1558Glu) c.882C>A c.4594C>A c.4226C>A (p.Ala1409Glu) c.3503C>A (p.Ala1168Glu) c.497C>A (p.Ala166Glu) n.3964C>A c.3041C>A (p.Ala1014Glu) n.4821C>A n.4804C>A | dbSNP |
| 12 | g.45852796C>G | CA384492248 | ARID2 | c.4673C>G (p.Ala1558Gly) c.882C>G c.4594C>G c.4226C>G (p.Ala1409Gly) c.3503C>G (p.Ala1168Gly) c.497C>G (p.Ala166Gly) n.3964C>G c.3041C>G (p.Ala1014Gly) n.4821C>G n.4804C>G | dbSNP |
| 12 | g.45852796C>T | CA384492246 | ARID2 | c.4673C>T (p.Ala1558Val) c.882C>T c.4594C>T c.4226C>T (p.Ala1409Val) c.3503C>T (p.Ala1168Val) c.497C>T (p.Ala166Val) n.3964C>T c.3041C>T (p.Ala1014Val) n.4821C>T n.4804C>T | dbSNP |
| 12 | g.45852797A= | CA2033475779 | ARID2 | c.4674A= (p.Ala1558=) c.883A= c.4595A= c.4227A= (p.Ala1409=) c.3504A= (p.Ala1168=) c.498A= (p.Ala166=) n.3965A= c.3042A= (p.Ala1014=) n.4822A= n.4805A= | |
| 12 | g.45852797A>C | CA479694186 | ARID2 | c.4674A>C (p.Ala1558=) c.883A>C c.4595A>C c.4227A>C (p.Ala1409=) c.3504A>C (p.Ala1168=) c.498A>C (p.Ala166=) n.3965A>C c.3042A>C (p.Ala1014=) n.4822A>C n.4805A>C | |
| 12 | g.45852797A>G | CA479694187 | ARID2 | c.4674A>G (p.Ala1558=) c.883A>G c.4595A>G c.4227A>G (p.Ala1409=) c.3504A>G (p.Ala1168=) c.498A>G (p.Ala166=) n.3965A>G c.3042A>G (p.Ala1014=) n.4822A>G n.4805A>G | dbSNP gnomAD v4 |
| 12 | g.45852797A>T | CA479694188 | ARID2 | c.4674A>T (p.Ala1558=) c.883A>T c.4595A>T c.4227A>T (p.Ala1409=) c.3504A>T (p.Ala1168=) c.498A>T (p.Ala166=) n.3965A>T c.3042A>T (p.Ala1014=) n.4822A>T n.4805A>T | |
| 12 | g.45852798G>A | CA384492251 | ARID2 | c.4675G>A (p.Gly1559Arg) c.884G>A c.4596G>A c.4228G>A (p.Gly1410Arg) c.3505G>A (p.Gly1169Arg) c.499G>A (p.Gly167Arg) n.3966G>A c.3043G>A (p.Gly1015Arg) n.4823G>A n.4806G>A | dbSNP |
| 12 | g.45852798G>C | CA384492256 | ARID2 | c.4675G>C (p.Gly1559Arg) c.884G>C c.4596G>C c.4228G>C (p.Gly1410Arg) c.3505G>C (p.Gly1169Arg) c.499G>C (p.Gly167Arg) n.3966G>C c.3043G>C (p.Gly1015Arg) n.4823G>C n.4806G>C | |
| 12 | g.45852798G>T | CA384492254 | ARID2 | c.4675G>T (p.Gly1559Ter) c.884G>T c.4596G>T c.4228G>T (p.Gly1410Ter) c.3505G>T (p.Gly1169Ter) c.499G>T (p.Gly167Ter) n.3966G>T c.3043G>T (p.Gly1015Ter) n.4823G>T n.4806G>T | dbSNP COSMIC |
| 12 | g.45852799G>A | CA384492259 | ARID2 | c.4676G>A (p.Gly1559Glu) c.885G>A c.4597G>A c.4229G>A (p.Gly1410Glu) c.3506G>A (p.Gly1169Glu) c.500G>A (p.Gly167Glu) n.3967G>A c.3044G>A (p.Gly1015Glu) n.4824G>A n.4807G>A | dbSNP |
| 12 | g.45852799G>C | CA384492263 | ARID2 | c.4676G>C (p.Gly1559Ala) c.885G>C c.4597G>C c.4229G>C (p.Gly1410Ala) c.3506G>C (p.Gly1169Ala) c.500G>C (p.Gly167Ala) n.3967G>C c.3044G>C (p.Gly1015Ala) n.4824G>C n.4807G>C | dbSNP |
| 12 | g.45852799G>T | CA384492261 | ARID2 | c.4676G>T (p.Gly1559Val) c.885G>T c.4597G>T c.4229G>T (p.Gly1410Val) c.3506G>T (p.Gly1169Val) c.500G>T (p.Gly167Val) n.3967G>T c.3044G>T (p.Gly1015Val) n.4824G>T n.4807G>T | |
| 12 | g.45852800A>C | CA479694190 | ARID2 | c.4677A>C (p.Gly1559=) c.886A>C c.4598A>C c.4230A>C (p.Gly1410=) c.3507A>C (p.Gly1169=) c.501A>C (p.Gly167=) n.3968A>C c.3045A>C (p.Gly1015=) n.4825A>C n.4808A>C | |
| 12 | g.45852800A>G | CA479694191 | ARID2 | c.4677A>G (p.Gly1559=) c.886A>G c.4598A>G c.4230A>G (p.Gly1410=) c.3507A>G (p.Gly1169=) c.501A>G (p.Gly167=) n.3968A>G c.3045A>G (p.Gly1015=) n.4825A>G n.4808A>G | dbSNP |
| 12 | g.45852800A>T | CA479694192 | ARID2 | c.4677A>T (p.Gly1559=) c.886A>T c.4598A>T c.4230A>T (p.Gly1410=) c.3507A>T (p.Gly1169=) c.501A>T (p.Gly167=) n.3968A>T c.3045A>T (p.Gly1015=) n.4825A>T n.4808A>T | dbSNP |
| 12 | g.45852801G>A | CA6526704 | ARID2 | c.4678G>A (p.Ala1560Thr) c.887G>A c.4599G>A c.4231G>A (p.Ala1411Thr) c.3508G>A (p.Ala1170Thr) c.502G>A (p.Ala168Thr) n.3969G>A c.3046G>A (p.Ala1016Thr) n.4826G>A n.4809G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.45852801G>C | CA384492268 | ARID2 | c.4678G>C (p.Ala1560Pro) c.887G>C c.4599G>C c.4231G>C (p.Ala1411Pro) c.3508G>C (p.Ala1170Pro) c.502G>C (p.Ala168Pro) n.3969G>C c.3046G>C (p.Ala1016Pro) n.4826G>C n.4809G>C | dbSNP |
| 12 | g.45852801G= | CA2033475780 | ARID2 | c.4678G= (p.Ala1560=) c.887G= c.4599G= c.4231G= (p.Ala1411=) c.3508G= (p.Ala1170=) c.502G= (p.Ala168=) n.3969G= c.3046G= (p.Ala1016=) n.4826G= n.4809G= | |
| 12 | g.45852801G>T | CA384492270 | ARID2 | c.4678G>T (p.Ala1560Ser) c.887G>T c.4599G>T c.4231G>T (p.Ala1411Ser) c.3508G>T (p.Ala1170Ser) c.502G>T (p.Ala168Ser) n.3969G>T c.3046G>T (p.Ala1016Ser) n.4826G>T n.4809G>T | |
| 12 | g.45852802C>A | CA384492273 | ARID2 | c.4679C>A (p.Ala1560Glu) c.888C>A c.4600C>A c.4232C>A (p.Ala1411Glu) c.3509C>A (p.Ala1170Glu) c.503C>A (p.Ala168Glu) n.3970C>A c.3047C>A (p.Ala1016Glu) n.4827C>A n.4810C>A | dbSNP |
| 12 | g.45852802C>G | CA384492275 | ARID2 | c.4679C>G (p.Ala1560Gly) c.888C>G c.4600C>G c.4232C>G (p.Ala1411Gly) c.3509C>G (p.Ala1170Gly) c.503C>G (p.Ala168Gly) n.3970C>G c.3047C>G (p.Ala1016Gly) n.4827C>G n.4810C>G | dbSNP |
| 12 | g.45852802C>T | CA384492277 | ARID2 | c.4679C>T (p.Ala1560Val) c.888C>T c.4600C>T c.4232C>T (p.Ala1411Val) c.3509C>T (p.Ala1170Val) c.503C>T (p.Ala168Val) n.3970C>T c.3047C>T (p.Ala1016Val) n.4827C>T n.4810C>T | dbSNP gnomAD v4 |
| 12 | g.45852803A>C | CA479694196 | ARID2 | c.4680A>C (p.Ala1560=) c.889A>C c.4601A>C c.4233A>C (p.Ala1411=) c.3510A>C (p.Ala1170=) c.504A>C (p.Ala168=) n.3971A>C c.3048A>C (p.Ala1016=) n.4828A>C n.4811A>C | |
| 12 | g.45852803A>G | CA479694195 | ARID2 | c.4680A>G (p.Ala1560=) c.889A>G c.4601A>G c.4233A>G (p.Ala1411=) c.3510A>G (p.Ala1170=) c.504A>G (p.Ala168=) n.3971A>G c.3048A>G (p.Ala1016=) n.4828A>G n.4811A>G | dbSNP |
| 12 | g.45852803A>T | CA479694193 | ARID2 | c.4680A>T (p.Ala1560=) c.889A>T c.4601A>T c.4233A>T (p.Ala1411=) c.3510A>T (p.Ala1170=) c.504A>T (p.Ala168=) n.3971A>T c.3048A>T (p.Ala1016=) n.4828A>T n.4811A>T | |
| 12 | g.45852804G>A | CA384492279 | ARID2 | c.4681G>A (p.Asp1561Asn) c.890G>A c.4602G>A c.4234G>A (p.Asp1412Asn) c.3511G>A (p.Asp1171Asn) c.505G>A (p.Asp169Asn) n.3972G>A c.3049G>A (p.Asp1017Asn) n.4829G>A n.4812G>A | dbSNP |
| 12 | g.45852804G>C | CA384492282 | ARID2 | c.4681G>C (p.Asp1561His) c.890G>C c.4602G>C c.4234G>C (p.Asp1412His) c.3511G>C (p.Asp1171His) c.505G>C (p.Asp169His) n.3972G>C c.3049G>C (p.Asp1017His) n.4829G>C n.4812G>C | dbSNP |
| 12 | g.45852804G>T | CA384492284 | ARID2 | c.4681G>T (p.Asp1561Tyr) c.890G>T c.4602G>T c.4234G>T (p.Asp1412Tyr) c.3511G>T (p.Asp1171Tyr) c.505G>T (p.Asp169Tyr) n.3972G>T c.3049G>T (p.Asp1017Tyr) n.4829G>T n.4812G>T | dbSNP |
| 12 | g.45852805A>C | CA384492288 | ARID2 | c.4682A>C (p.Asp1561Ala) c.891A>C c.4603A>C c.4235A>C (p.Asp1412Ala) c.3512A>C (p.Asp1171Ala) c.506A>C (p.Asp169Ala) n.3973A>C c.3050A>C (p.Asp1017Ala) n.4830A>C n.4813A>C | dbSNP |
| 12 | g.45852805A>G | CA384492289 | ARID2 | c.4682A>G (p.Asp1561Gly) c.891A>G c.4603A>G c.4235A>G (p.Asp1412Gly) c.3512A>G (p.Asp1171Gly) c.506A>G (p.Asp169Gly) n.3973A>G c.3050A>G (p.Asp1017Gly) n.4830A>G n.4813A>G | |
| 12 | g.45852805A>T | CA384492291 | ARID2 | c.4682A>T (p.Asp1561Val) c.891A>T c.4603A>T c.4235A>T (p.Asp1412Val) c.3512A>T (p.Asp1171Val) c.506A>T (p.Asp169Val) n.3973A>T c.3050A>T (p.Asp1017Val) n.4830A>T n.4813A>T | dbSNP |
| 12 | g.45852806T>A | CA384492296 | ARID2 | c.4683T>A (p.Asp1561Glu) c.892T>A c.4604T>A c.4236T>A (p.Asp1412Glu) c.3513T>A (p.Asp1171Glu) c.507T>A (p.Asp169Glu) n.3974T>A c.3051T>A (p.Asp1017Glu) n.4831T>A n.4814T>A | |
| 12 | g.45852806T>C | CA479694200 | ARID2 | c.4683T>C (p.Asp1561=) c.892T>C c.4604T>C c.4236T>C (p.Asp1412=) c.3513T>C (p.Asp1171=) c.507T>C (p.Asp169=) n.3974T>C c.3051T>C (p.Asp1017=) n.4831T>C n.4814T>C | |
| 12 | g.45852806T>G | CA384492294 | ARID2 | c.4683T>G (p.Asp1561Glu) c.892T>G c.4604T>G c.4236T>G (p.Asp1412Glu) c.3513T>G (p.Asp1171Glu) c.507T>G (p.Asp169Glu) n.3974T>G c.3051T>G (p.Asp1017Glu) n.4831T>G n.4814T>G | |
| 12 | g.45852807C>A | CA384492299 | ARID2 | c.4684C>A (p.Pro1562Thr) c.893C>A c.4605C>A c.4237C>A (p.Pro1413Thr) c.3514C>A (p.Pro1172Thr) c.508C>A (p.Pro170Thr) n.3975C>A c.3052C>A (p.Pro1018Thr) n.4832C>A n.4815C>A | dbSNP |
| 12 | g.45852807C= | CA2033475781 | ARID2 | c.4684C= (p.Pro1562=) c.893C= c.4605C= c.4237C= (p.Pro1413=) c.3514C= (p.Pro1172=) c.508C= (p.Pro170=) n.3975C= c.3052C= (p.Pro1018=) n.4832C= n.4815C= | |
| 12 | g.45852807C>G | CA384492301 | ARID2 | c.4684C>G (p.Pro1562Ala) c.893C>G c.4605C>G c.4237C>G (p.Pro1413Ala) c.3514C>G (p.Pro1172Ala) c.508C>G (p.Pro170Ala) n.3975C>G c.3052C>G (p.Pro1018Ala) n.4832C>G n.4815C>G | dbSNP |
| 12 | g.45852807C>T | CA384492303 | ARID2 | c.4684C>T (p.Pro1562Ser) c.893C>T c.4605C>T c.4237C>T (p.Pro1413Ser) c.3514C>T (p.Pro1172Ser) c.508C>T (p.Pro170Ser) n.3975C>T c.3052C>T (p.Pro1018Ser) n.4832C>T n.4815C>T | dbSNP |
| 12 | g.45852807_45852808insAGCA | CA658786243 | ARID2 | c.4684_4685insAGCA (p.Pro1562GlnfsTer7) c.893_894insAGCA c.4605_4606insAGCA c.4237_4238insAGCA (p.Pro1413GlnfsTer7) c.3514_3515insAGCA (p.Pro1172GlnfsTer7) c.508_509insAGCA (p.Pro170GlnfsTer7) n.3975_3976insAGCA c.3052_3053insAGCA (p.Pro1018GlnfsTer7) n.4832_4833insAGCA n.4815_4816insAGCA | |
| 12 | g.45852808C>A | CA384492307 | ARID2 | c.4685C>A (p.Pro1562Gln) c.894C>A c.4606C>A c.4238C>A (p.Pro1413Gln) c.3515C>A (p.Pro1172Gln) c.509C>A (p.Pro170Gln) n.3976C>A c.3053C>A (p.Pro1018Gln) n.4833C>A n.4816C>A | dbSNP |
| 12 | g.45852808C>G | CA384492309 | ARID2 | c.4685C>G (p.Pro1562Arg) c.894C>G c.4606C>G c.4238C>G (p.Pro1413Arg) c.3515C>G (p.Pro1172Arg) c.509C>G (p.Pro170Arg) n.3976C>G c.3053C>G (p.Pro1018Arg) n.4833C>G n.4816C>G | dbSNP |
| 12 | g.45852808C>T | CA384492311 | ARID2 | c.4685C>T (p.Pro1562Leu) c.894C>T c.4606C>T c.4238C>T (p.Pro1413Leu) c.3515C>T (p.Pro1172Leu) c.509C>T (p.Pro170Leu) n.3976C>T c.3053C>T (p.Pro1018Leu) n.4833C>T n.4816C>T | dbSNP COSMIC |
| 12 | g.45852810_45852813dup | CA2695216574 | ARID2 | c.4687_4690dup (p.Thr1564LysfsTer5) c.896_899dup c.4608_4611dup c.4240_4243dup (p.Thr1415LysfsTer5) c.3517_3520dup (p.Thr1174LysfsTer5) c.511_514dup (p.Thr172LysfsTer5) n.3978_3981dup c.3055_3058dup (p.Thr1020LysfsTer5) n.4835_4838dup n.4818_4821dup | |
| 12 | g.45852809A>C | CA479694202 | ARID2 | c.4686A>C (p.Pro1562=) c.895A>C c.4607A>C c.4239A>C (p.Pro1413=) c.3516A>C (p.Pro1172=) c.510A>C (p.Pro170=) n.3977A>C c.3054A>C (p.Pro1018=) n.4834A>C n.4817A>C | |
| 12 | g.45852809A>G | CA479694203 | ARID2 | c.4686A>G (p.Pro1562=) c.895A>G c.4607A>G c.4239A>G (p.Pro1413=) c.3516A>G (p.Pro1172=) c.510A>G (p.Pro170=) n.3977A>G c.3054A>G (p.Pro1018=) n.4834A>G n.4817A>G | dbSNP gnomAD v4 |
| 12 | g.45852809A>T | CA479694204 | ARID2 | c.4686A>T (p.Pro1562=) c.895A>T c.4607A>T c.4239A>T (p.Pro1413=) c.3516A>T (p.Pro1172=) c.510A>T (p.Pro170=) n.3977A>T c.3054A>T (p.Pro1018=) n.4834A>T n.4817A>T | dbSNP |
| 12 | g.45852810A>C | CA384492315 | ARID2 | c.4687A>C (p.Ser1563Arg) c.896A>C c.4608A>C c.4240A>C (p.Ser1414Arg) c.3517A>C (p.Ser1173Arg) c.511A>C (p.Ser171Arg) n.3978A>C c.3055A>C (p.Ser1019Arg) n.4835A>C n.4818A>C | dbSNP |
| 12 | g.45852810A>G | CA384492316 | ARID2 | c.4687A>G (p.Ser1563Gly) c.896A>G c.4608A>G c.4240A>G (p.Ser1414Gly) c.3517A>G (p.Ser1173Gly) c.511A>G (p.Ser171Gly) n.3978A>G c.3055A>G (p.Ser1019Gly) n.4835A>G n.4818A>G | dbSNP |
| 12 | g.45852810A>T | CA384492318 | ARID2 | c.4687A>T (p.Ser1563Cys) c.896A>T c.4608A>T c.4240A>T (p.Ser1414Cys) c.3517A>T (p.Ser1173Cys) c.511A>T (p.Ser171Cys) n.3978A>T c.3055A>T (p.Ser1019Cys) n.4835A>T n.4818A>T | dbSNP |
| 12 | g.45852811G>A | CA384492321 | ARID2 | c.4688G>A (p.Ser1563Asn) c.897G>A c.4609G>A c.4241G>A (p.Ser1414Asn) c.3518G>A (p.Ser1173Asn) c.512G>A (p.Ser171Asn) n.3979G>A c.3056G>A (p.Ser1019Asn) n.4836G>A n.4819G>A | dbSNP |
| 12 | g.45852811G>C | CA384492323 | ARID2 | c.4688G>C (p.Ser1563Thr) c.897G>C c.4609G>C c.4241G>C (p.Ser1414Thr) c.3518G>C (p.Ser1173Thr) c.512G>C (p.Ser171Thr) n.3979G>C c.3056G>C (p.Ser1019Thr) n.4836G>C n.4819G>C | dbSNP COSMIC |
| 12 | g.45852811G>T | CA384492325 | ARID2 | c.4688G>T (p.Ser1563Ile) c.897G>T c.4609G>T c.4241G>T (p.Ser1414Ile) c.3518G>T (p.Ser1173Ile) c.512G>T (p.Ser171Ile) n.3979G>T c.3056G>T (p.Ser1019Ile) n.4836G>T n.4819G>T | |
| 12 | g.45852812C>A | CA384492329 | ARID2 | c.4689C>A (p.Ser1563Arg) c.898C>A c.4610C>A c.4242C>A (p.Ser1414Arg) c.3519C>A (p.Ser1173Arg) c.513C>A (p.Ser171Arg) n.3980C>A c.3057C>A (p.Ser1019Arg) n.4837C>A n.4820C>A | dbSNP |
| 12 | g.45852812C>G | CA384492331 | ARID2 | c.4689C>G (p.Ser1563Arg) c.898C>G c.4610C>G c.4242C>G (p.Ser1414Arg) c.3519C>G (p.Ser1173Arg) c.513C>G (p.Ser171Arg) n.3980C>G c.3057C>G (p.Ser1019Arg) n.4837C>G n.4820C>G | dbSNP |
| 12 | g.45852812C>T | CA479694205 | ARID2 | c.4689C>T (p.Ser1563=) c.898C>T c.4610C>T c.4242C>T (p.Ser1414=) c.3519C>T (p.Ser1173=) c.513C>T (p.Ser171=) n.3980C>T c.3057C>T (p.Ser1019=) n.4837C>T n.4820C>T | dbSNP |
| 12 | g.45852813A>C | CA384492334 | ARID2 | c.4690A>C (p.Thr1564Pro) c.899A>C c.4611A>C c.4243A>C (p.Thr1415Pro) c.3520A>C (p.Thr1174Pro) c.514A>C (p.Thr172Pro) n.3981A>C c.3058A>C (p.Thr1020Pro) n.4838A>C n.4821A>C | dbSNP |
| 12 | g.45852813A>G | CA384492335 | ARID2 | c.4690A>G (p.Thr1564Ala) c.899A>G c.4611A>G c.4243A>G (p.Thr1415Ala) c.3520A>G (p.Thr1174Ala) c.514A>G (p.Thr172Ala) n.3981A>G c.3058A>G (p.Thr1020Ala) n.4838A>G n.4821A>G | |
| 12 | g.45852813A>T | CA384492337 | ARID2 | c.4690A>T (p.Thr1564Ser) c.899A>T c.4611A>T c.4243A>T (p.Thr1415Ser) c.3520A>T (p.Thr1174Ser) c.514A>T (p.Thr172Ser) n.3981A>T c.3058A>T (p.Thr1020Ser) n.4838A>T n.4821A>T | dbSNP |
| 12 | g.45852814C>A | CA384492340 | ARID2 | c.4691C>A (p.Thr1564Asn) c.900C>A c.4612C>A c.4244C>A (p.Thr1415Asn) c.3521C>A (p.Thr1174Asn) c.515C>A (p.Thr172Asn) n.3982C>A c.3059C>A (p.Thr1020Asn) n.4839C>A n.4822C>A | dbSNP |
| 12 | g.45852814C>G | CA384492342 | ARID2 | c.4691C>G (p.Thr1564Ser) c.900C>G c.4612C>G c.4244C>G (p.Thr1415Ser) c.3521C>G (p.Thr1174Ser) c.515C>G (p.Thr172Ser) n.3982C>G c.3059C>G (p.Thr1020Ser) n.4839C>G n.4822C>G | dbSNP gnomAD v4 |
| 12 | g.45852814C>T | CA384492344 | ARID2 | c.4691C>T (p.Thr1564Ile) c.900C>T c.4612C>T c.4244C>T (p.Thr1415Ile) c.3521C>T (p.Thr1174Ile) c.515C>T (p.Thr172Ile) n.3982C>T c.3059C>T (p.Thr1020Ile) n.4839C>T n.4822C>T | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852815T>A | CA479694208 | ARID2 | c.4692T>A (p.Thr1564=) c.901T>A c.4613T>A c.4245T>A (p.Thr1415=) c.3522T>A (p.Thr1174=) c.516T>A (p.Thr172=) n.3983T>A c.3060T>A (p.Thr1020=) n.4840T>A n.4823T>A | dbSNP |
| 12 | g.45852815T>C | CA479694209 | ARID2 | c.4692T>C (p.Thr1564=) c.901T>C c.4613T>C c.4245T>C (p.Thr1415=) c.3522T>C (p.Thr1174=) c.516T>C (p.Thr172=) n.3983T>C c.3060T>C (p.Thr1020=) n.4840T>C n.4823T>C | ClinVar dbSNP |
| 12 | g.45852815T>G | CA236400964 | ARID2 | c.4692T>G (p.Thr1564=) c.901T>G c.4613T>G c.4245T>G (p.Thr1415=) c.3522T>G (p.Thr1174=) c.516T>G (p.Thr172=) n.3983T>G c.3060T>G (p.Thr1020=) n.4840T>G n.4823T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852815T= | CA2033475782 | ARID2 | c.4692T= (p.Thr1564=) c.901T= c.4613T= c.4245T= (p.Thr1415=) c.3522T= (p.Thr1174=) c.516T= (p.Thr172=) n.3983T= c.3060T= (p.Thr1020=) n.4840T= n.4823T= | |
| 12 | g.45852816G>A | CA6526705 | ARID2 | c.4693G>A (p.Val1565Ile) c.902G>A c.4614G>A c.4246G>A (p.Val1416Ile) c.3523G>A (p.Val1175Ile) c.517G>A (p.Val173Ile) n.3984G>A c.3061G>A (p.Val1021Ile) n.4841G>A n.4824G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852816G>C | CA384492348 | ARID2 | c.4693G>C (p.Val1565Leu) c.902G>C c.4614G>C c.4246G>C (p.Val1416Leu) c.3523G>C (p.Val1175Leu) c.517G>C (p.Val173Leu) n.3984G>C c.3061G>C (p.Val1021Leu) n.4841G>C n.4824G>C | |
| 12 | g.45852816G= | CA2033475783 | ARID2 | c.4693G= (p.Val1565=) c.902G= c.4614G= c.4246G= (p.Val1416=) c.3523G= (p.Val1175=) c.517G= (p.Val173=) n.3984G= c.3061G= (p.Val1021=) n.4841G= n.4824G= | |
| 12 | g.45852816G>T | CA384492351 | ARID2 | c.4693G>T (p.Val1565Leu) c.902G>T c.4614G>T c.4246G>T (p.Val1416Leu) c.3523G>T (p.Val1175Leu) c.517G>T (p.Val173Leu) n.3984G>T c.3061G>T (p.Val1021Leu) n.4841G>T n.4824G>T | |
| 12 | g.45852817T>A | CA384492354 | ARID2 | c.4694T>A (p.Val1565Glu) c.903T>A c.4615T>A c.4247T>A (p.Val1416Glu) c.3524T>A (p.Val1175Glu) c.518T>A (p.Val173Glu) n.3985T>A c.3062T>A (p.Val1021Glu) n.4842T>A n.4825T>A | dbSNP |
| 12 | g.45852817T>C | CA384492355 | ARID2 | c.4694T>C (p.Val1565Ala) c.903T>C c.4615T>C c.4247T>C (p.Val1416Ala) c.3524T>C (p.Val1175Ala) c.518T>C (p.Val173Ala) n.3985T>C c.3062T>C (p.Val1021Ala) n.4842T>C n.4825T>C | dbSNP gnomAD v4 |
| 12 | g.45852817T>G | CA384492358 | ARID2 | c.4694T>G (p.Val1565Gly) c.903T>G c.4615T>G c.4247T>G (p.Val1416Gly) c.3524T>G (p.Val1175Gly) c.518T>G (p.Val173Gly) n.3985T>G c.3062T>G (p.Val1021Gly) n.4842T>G n.4825T>G | ClinVar dbSNP |
| 12 | g.45852818A= | CA2033475784 | ARID2 | c.4695A= (p.Val1565=) c.904A= c.4616A= c.4248A= (p.Val1416=) c.3525A= (p.Val1175=) c.519A= (p.Val173=) n.3986A= c.3063A= (p.Val1021=) n.4843A= n.4826A= | |
| 12 | g.45852818A>C | CA479694214 | ARID2 | c.4695A>C (p.Val1565=) c.904A>C c.4616A>C c.4248A>C (p.Val1416=) c.3525A>C (p.Val1175=) c.519A>C (p.Val173=) n.3986A>C c.3063A>C (p.Val1021=) n.4843A>C n.4826A>C | |
| 12 | g.45852818A>G | CA479694215 | ARID2 | c.4695A>G (p.Val1565=) c.904A>G c.4616A>G c.4248A>G (p.Val1416=) c.3525A>G (p.Val1175=) c.519A>G (p.Val173=) n.3986A>G c.3063A>G (p.Val1021=) n.4843A>G n.4826A>G | dbSNP |
| 12 | g.45852818A>T | CA479694216 | ARID2 | c.4695A>T (p.Val1565=) c.904A>T c.4616A>T c.4248A>T (p.Val1416=) c.3525A>T (p.Val1175=) c.519A>T (p.Val173=) n.3986A>T c.3063A>T (p.Val1021=) n.4843A>T n.4826A>T | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852819G>A | CA384492367 | ARID2 | c.4696G>A (p.Ala1566Thr) c.905G>A c.4617G>A c.4249G>A (p.Ala1417Thr) c.3526G>A (p.Ala1176Thr) c.520G>A (p.Ala174Thr) n.3987G>A c.3064G>A (p.Ala1022Thr) n.4844G>A n.4827G>A | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852819G>C | CA384492363 | ARID2 | c.4696G>C (p.Ala1566Pro) c.905G>C c.4617G>C c.4249G>C (p.Ala1417Pro) c.3526G>C (p.Ala1176Pro) c.520G>C (p.Ala174Pro) n.3987G>C c.3064G>C (p.Ala1022Pro) n.4844G>C n.4827G>C | dbSNP |
| 12 | g.45852819G= | CA2033475785 | ARID2 | c.4696G= (p.Ala1566=) c.905G= c.4617G= c.4249G= (p.Ala1417=) c.3526G= (p.Ala1176=) c.520G= (p.Ala174=) n.3987G= c.3064G= (p.Ala1022=) n.4844G= n.4827G= | |
| 12 | g.45852819G>T | CA384492364 | ARID2 | c.4696G>T (p.Ala1566Ser) c.905G>T c.4617G>T c.4249G>T (p.Ala1417Ser) c.3526G>T (p.Ala1176Ser) c.520G>T (p.Ala174Ser) n.3987G>T c.3064G>T (p.Ala1022Ser) n.4844G>T n.4827G>T | dbSNP |
| 12 | g.45852820C>A | CA384492371 | ARID2 | c.4697C>A (p.Ala1566Asp) c.906C>A c.4618C>A c.4250C>A (p.Ala1417Asp) c.3527C>A (p.Ala1176Asp) c.521C>A (p.Ala174Asp) n.3988C>A c.3065C>A (p.Ala1022Asp) n.4845C>A n.4828C>A | dbSNP |
| 12 | g.45852820C>G | CA384492373 | ARID2 | c.4697C>G (p.Ala1566Gly) c.906C>G c.4618C>G c.4250C>G (p.Ala1417Gly) c.3527C>G (p.Ala1176Gly) c.521C>G (p.Ala174Gly) n.3988C>G c.3065C>G (p.Ala1022Gly) n.4845C>G n.4828C>G | dbSNP |
| 12 | g.45852820C>T | CA384492375 | ARID2 | c.4697C>T (p.Ala1566Val) c.906C>T c.4618C>T c.4250C>T (p.Ala1417Val) c.3527C>T (p.Ala1176Val) c.521C>T (p.Ala174Val) n.3988C>T c.3065C>T (p.Ala1022Val) n.4845C>T n.4828C>T | |
| 12 | g.45852821T>A | CA479694217 | ARID2 | c.4698T>A (p.Ala1566=) c.907T>A c.4619T>A c.4251T>A (p.Ala1417=) c.3528T>A (p.Ala1176=) c.522T>A (p.Ala174=) n.3989T>A c.3066T>A (p.Ala1022=) n.4846T>A n.4829T>A | |
| 12 | g.45852821T>C | CA479694219 | ARID2 | c.4698T>C (p.Ala1566=) c.907T>C c.4619T>C c.4251T>C (p.Ala1417=) c.3528T>C (p.Ala1176=) c.522T>C (p.Ala174=) n.3989T>C c.3066T>C (p.Ala1022=) n.4846T>C n.4829T>C | |
| 12 | g.45852821T>G | CA479694220 | ARID2 | c.4698T>G (p.Ala1566=) c.907T>G c.4619T>G c.4251T>G (p.Ala1417=) c.3528T>G (p.Ala1176=) c.522T>G (p.Ala174=) n.3989T>G c.3066T>G (p.Ala1022=) n.4846T>G n.4829T>G | |
| 12 | g.45852822A>C | CA384492378 | ARID2 | c.4699A>C (p.Lys1567Gln) c.908A>C c.4620A>C c.4252A>C (p.Lys1418Gln) c.3529A>C (p.Lys1177Gln) c.523A>C (p.Lys175Gln) n.3990A>C c.3067A>C (p.Lys1023Gln) n.4847A>C n.4830A>C | |
| 12 | g.45852822A>G | CA384492380 | ARID2 | c.4699A>G (p.Lys1567Glu) c.908A>G c.4620A>G c.4252A>G (p.Lys1418Glu) c.3529A>G (p.Lys1177Glu) c.523A>G (p.Lys175Glu) n.3990A>G c.3067A>G (p.Lys1023Glu) n.4847A>G n.4830A>G | dbSNP |
| 12 | g.45852822A>T | CA384492382 | ARID2 | c.4699A>T (p.Lys1567Ter) c.908A>T c.4620A>T c.4252A>T (p.Lys1418Ter) c.3529A>T (p.Lys1177Ter) c.523A>T (p.Lys175Ter) n.3990A>T c.3067A>T (p.Lys1023Ter) n.4847A>T n.4830A>T | dbSNP |
| 12 | g.45852823A>C | CA384492386 | ARID2 | c.4700A>C (p.Lys1567Thr) c.909A>C c.4621A>C c.4253A>C (p.Lys1418Thr) c.3530A>C (p.Lys1177Thr) c.524A>C (p.Lys175Thr) n.3991A>C c.3068A>C (p.Lys1023Thr) n.4848A>C n.4831A>C | dbSNP |
| 12 | g.45852823A>G | CA384492388 | ARID2 | c.4700A>G (p.Lys1567Arg) c.909A>G c.4621A>G c.4253A>G (p.Lys1418Arg) c.3530A>G (p.Lys1177Arg) c.524A>G (p.Lys175Arg) n.3991A>G c.3068A>G (p.Lys1023Arg) n.4848A>G n.4831A>G | |
| 12 | g.45852823A>T | CA384492390 | ARID2 | c.4700A>T (p.Lys1567Ile) c.909A>T c.4621A>T c.4253A>T (p.Lys1418Ile) c.3530A>T (p.Lys1177Ile) c.524A>T (p.Lys175Ile) n.3991A>T c.3068A>T (p.Lys1023Ile) n.4848A>T n.4831A>T | dbSNP |
| 12 | g.45852824A>C | CA384492393 | ARID2 | c.4701A>C (p.Lys1567Asn) c.910A>C c.4622A>C c.4254A>C (p.Lys1418Asn) c.3531A>C (p.Lys1177Asn) c.525A>C (p.Lys175Asn) n.3992A>C c.3069A>C (p.Lys1023Asn) n.4849A>C n.4832A>C | |
| 12 | g.45852824A>G | CA479694224 | ARID2 | c.4701A>G (p.Lys1567=) c.910A>G c.4622A>G c.4254A>G (p.Lys1418=) c.3531A>G (p.Lys1177=) c.525A>G (p.Lys175=) n.3992A>G c.3069A>G (p.Lys1023=) n.4849A>G n.4832A>G | |
| 12 | g.45852824A>T | CA384492395 | ARID2 | c.4701A>T (p.Lys1567Asn) c.910A>T c.4622A>T c.4254A>T (p.Lys1418Asn) c.3531A>T (p.Lys1177Asn) c.525A>T (p.Lys175Asn) n.3992A>T c.3069A>T (p.Lys1023Asn) n.4849A>T n.4832A>T | dbSNP |
| 12 | g.45852825G>A | CA384492403 | ARID2 | c.4702G>A (p.Val1568Ile) c.911G>A c.4623G>A c.4255G>A (p.Val1419Ile) c.3532G>A (p.Val1178Ile) c.526G>A (p.Val176Ile) n.3993G>A c.3070G>A (p.Val1024Ile) n.4850G>A n.4833G>A | dbSNP |
| 12 | g.45852825G>C | CA384492400 | ARID2 | c.4702G>C (p.Val1568Leu) c.911G>C c.4623G>C c.4255G>C (p.Val1419Leu) c.3532G>C (p.Val1178Leu) c.526G>C (p.Val176Leu) n.3993G>C c.3070G>C (p.Val1024Leu) n.4850G>C n.4833G>C | dbSNP |
| 12 | g.45852825G>T | CA384492398 | ARID2 | c.4702G>T (p.Val1568Leu) c.911G>T c.4623G>T c.4255G>T (p.Val1419Leu) c.3532G>T (p.Val1178Leu) c.526G>T (p.Val176Leu) n.3993G>T c.3070G>T (p.Val1024Leu) n.4850G>T n.4833G>T | dbSNP |
| 12 | g.45852826T>A | CA384492406 | ARID2 | c.4703T>A (p.Val1568Glu) c.912T>A c.4624T>A c.4256T>A (p.Val1419Glu) c.3533T>A (p.Val1178Glu) c.527T>A (p.Val176Glu) n.3994T>A c.3071T>A (p.Val1024Glu) n.4851T>A n.4834T>A | dbSNP |
| 12 | g.45852826T>C | CA384492411 | ARID2 | c.4703T>C (p.Val1568Ala) c.912T>C c.4624T>C c.4256T>C (p.Val1419Ala) c.3533T>C (p.Val1178Ala) c.527T>C (p.Val176Ala) n.3994T>C c.3071T>C (p.Val1024Ala) n.4851T>C n.4834T>C | |
| 12 | g.45852826T>G | CA384492409 | ARID2 | c.4703T>G (p.Val1568Gly) c.912T>G c.4624T>G c.4256T>G (p.Val1419Gly) c.3533T>G (p.Val1178Gly) c.527T>G (p.Val176Gly) n.3994T>G c.3071T>G (p.Val1024Gly) n.4851T>G n.4834T>G | |
| 12 | g.45852826dup | CA2739291636 | ARID2 | c.4703dup (p.Ala1569SerfsTer?) c.912dup c.4624dup c.4256dup (p.Ala1420SerfsTer?) c.3533dup (p.Ala1179SerfsTer?) c.527dup (p.Ala177SerfsTer?) n.3994dup c.3071dup (p.Ala1025SerfsTer?) n.4851dup n.4834dup | |
| 12 | g.45852827A>C | CA479694225 | ARID2 | c.4704A>C (p.Val1568=) c.913A>C c.4625A>C c.4257A>C (p.Val1419=) c.3534A>C (p.Val1178=) c.528A>C (p.Val176=) n.3995A>C c.3072A>C (p.Val1024=) n.4852A>C n.4835A>C | |
| 12 | g.45852827A>G | CA479694226 | ARID2 | c.4704A>G (p.Val1568=) c.913A>G c.4625A>G c.4257A>G (p.Val1419=) c.3534A>G (p.Val1178=) c.528A>G (p.Val176=) n.3995A>G c.3072A>G (p.Val1024=) n.4852A>G n.4835A>G | dbSNP |
| 12 | g.45852827A>T | CA479694227 | ARID2 | c.4704A>T (p.Val1568=) c.913A>T c.4625A>T c.4257A>T (p.Val1419=) c.3534A>T (p.Val1178=) c.528A>T (p.Val176=) n.3995A>T c.3072A>T (p.Val1024=) n.4852A>T n.4835A>T | dbSNP |
| 12 | g.45852828G>A | CA156970 | ARID2 | c.4705G>A (p.Ala1569Thr) c.914G>A c.4626G>A c.4258G>A (p.Ala1420Thr) c.3535G>A (p.Ala1179Thr) c.529G>A (p.Ala177Thr) n.3996G>A c.3073G>A (p.Ala1025Thr) n.4853G>A n.4836G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852828G>C | CA384492416 | ARID2 | c.4705G>C (p.Ala1569Pro) c.914G>C c.4626G>C c.4258G>C (p.Ala1420Pro) c.3535G>C (p.Ala1179Pro) c.529G>C (p.Ala177Pro) n.3996G>C c.3073G>C (p.Ala1025Pro) n.4853G>C n.4836G>C | dbSNP |
| 12 | g.45852828G= | CA2033475786 | ARID2 | c.4705G= (p.Ala1569=) c.914G= c.4626G= c.4258G= (p.Ala1420=) c.3535G= (p.Ala1179=) c.529G= (p.Ala177=) n.3996G= c.3073G= (p.Ala1025=) n.4853G= n.4836G= | |
| 12 | g.45852828G>T | CA384492418 | ARID2 | c.4705G>T (p.Ala1569Ser) c.914G>T c.4626G>T c.4258G>T (p.Ala1420Ser) c.3535G>T (p.Ala1179Ser) c.529G>T (p.Ala177Ser) n.3996G>T c.3073G>T (p.Ala1025Ser) n.4853G>T n.4836G>T | dbSNP |
| 12 | g.45852829C>A | CA384492421 | ARID2 | c.4706C>A (p.Ala1569Glu) c.915C>A c.4627C>A c.4259C>A (p.Ala1420Glu) c.3536C>A (p.Ala1179Glu) c.530C>A (p.Ala177Glu) n.3997C>A c.3074C>A (p.Ala1025Glu) n.4854C>A n.4837C>A | dbSNP |
| 12 | g.45852829C>G | CA384492423 | ARID2 | c.4706C>G (p.Ala1569Gly) c.915C>G c.4627C>G c.4259C>G (p.Ala1420Gly) c.3536C>G (p.Ala1179Gly) c.530C>G (p.Ala177Gly) n.3997C>G c.3074C>G (p.Ala1025Gly) n.4854C>G n.4837C>G | dbSNP |
| 12 | g.45852829C>T | CA384492425 | ARID2 | c.4706C>T (p.Ala1569Val) c.915C>T c.4627C>T c.4259C>T (p.Ala1420Val) c.3536C>T (p.Ala1179Val) c.530C>T (p.Ala177Val) n.3997C>T c.3074C>T (p.Ala1025Val) n.4854C>T n.4837C>T | dbSNP gnomAD v4 |
| 12 | g.45852830A>C | CA479694229 | ARID2 | c.4707A>C (p.Ala1569=) c.916A>C c.4628A>C c.4260A>C (p.Ala1420=) c.3537A>C (p.Ala1179=) c.531A>C (p.Ala177=) n.3998A>C c.3075A>C (p.Ala1025=) n.4855A>C n.4838A>C | |
| 12 | g.45852830A>G | CA479694230 | ARID2 | c.4707A>G (p.Ala1569=) c.916A>G c.4628A>G c.4260A>G (p.Ala1420=) c.3537A>G (p.Ala1179=) c.531A>G (p.Ala177=) n.3998A>G c.3075A>G (p.Ala1025=) n.4855A>G n.4838A>G | |
| 12 | g.45852830A>T | CA479694232 | ARID2 | c.4707A>T (p.Ala1569=) c.916A>T c.4628A>T c.4260A>T (p.Ala1420=) c.3537A>T (p.Ala1179=) c.531A>T (p.Ala177=) n.3998A>T c.3075A>T (p.Ala1025=) n.4855A>T n.4838A>T | dbSNP |
| 12 | g.45852831A>C | CA384492429 | ARID2 | c.4708A>C (p.Ile1570Leu) c.917A>C c.4629A>C c.4261A>C (p.Ile1421Leu) c.3538A>C (p.Ile1180Leu) c.532A>C (p.Ile178Leu) n.3999A>C c.3076A>C (p.Ile1026Leu) n.4856A>C n.4839A>C | dbSNP |
| 12 | g.45852831A>G | CA384492431 | ARID2 | c.4708A>G (p.Ile1570Val) c.917A>G c.4629A>G c.4261A>G (p.Ile1421Val) c.3538A>G (p.Ile1180Val) c.532A>G (p.Ile178Val) n.3999A>G c.3076A>G (p.Ile1026Val) n.4856A>G n.4839A>G | dbSNP gnomAD v4 |
| 12 | g.45852831A>T | CA384492433 | ARID2 | c.4708A>T (p.Ile1570Leu) c.917A>T c.4629A>T c.4261A>T (p.Ile1421Leu) c.3538A>T (p.Ile1180Leu) c.532A>T (p.Ile178Leu) n.3999A>T c.3076A>T (p.Ile1026Leu) n.4856A>T n.4839A>T | dbSNP |
| 12 | g.45852832T>A | CA384492437 | ARID2 | c.4709T>A (p.Ile1570Lys) c.918T>A c.4630T>A c.4262T>A (p.Ile1421Lys) c.3539T>A (p.Ile1180Lys) c.533T>A (p.Ile178Lys) n.4000T>A c.3077T>A (p.Ile1026Lys) n.4857T>A n.4840T>A | dbSNP |
| 12 | g.45852832T>C | CA384492438 | ARID2 | c.4709T>C (p.Ile1570Thr) c.918T>C c.4630T>C c.4262T>C (p.Ile1421Thr) c.3539T>C (p.Ile1180Thr) c.533T>C (p.Ile178Thr) n.4000T>C c.3077T>C (p.Ile1026Thr) n.4857T>C n.4840T>C | dbSNP |
| 12 | g.45852832T>G | CA384492439 | ARID2 | c.4709T>G (p.Ile1570Arg) c.918T>G c.4630T>G c.4262T>G (p.Ile1421Arg) c.3539T>G (p.Ile1180Arg) c.533T>G (p.Ile178Arg) n.4000T>G c.3077T>G (p.Ile1026Arg) n.4857T>G n.4840T>G | dbSNP |
| 12 | g.45852832T= | CA2033475788 | ARID2 | c.4709T= (p.Ile1570=) c.918T= c.4630T= c.4262T= (p.Ile1421=) c.3539T= (p.Ile1180=) c.533T= (p.Ile178=) n.4000T= c.3077T= (p.Ile1026=) n.4857T= n.4840T= | |
| 12 | g.45852832_45852835delinsTAGA | CA2033475787 | ARID2 | c.4709_4712delinsTAGA (p.Ile1570=) c.918_921delinsTAGA c.4630_4633delinsTAGA c.4262_4265delinsTAGA (p.Ile1421=) c.3539_3542delinsTAGA (p.Ile1180=) c.533_536delinsTAGA (p.Ile178=) n.4000_4003delinsTAGA c.3077_3080delinsTAGA (p.Ile1026=) n.4857_4860delinsTAGA n.4840_4843delinsTAGA | |
| 12 | g.45852833A>C | CA479694233 | ARID2 | c.4710A>C (p.Ile1570=) c.919A>C c.4631A>C c.4263A>C (p.Ile1421=) c.3540A>C (p.Ile1180=) c.534A>C (p.Ile178=) n.4001A>C c.3078A>C (p.Ile1026=) n.4858A>C n.4841A>C | |
| 12 | g.45852833A>G | CA384492442 | ARID2 | c.4710A>G (p.Ile1570Met) c.919A>G c.4631A>G c.4263A>G (p.Ile1421Met) c.3540A>G (p.Ile1180Met) c.534A>G (p.Ile178Met) n.4001A>G c.3078A>G (p.Ile1026Met) n.4858A>G n.4841A>G | |
| 12 | g.45852833A>T | CA479694234 | ARID2 | c.4710A>T (p.Ile1570=) c.919A>T c.4631A>T c.4263A>T (p.Ile1421=) c.3540A>T (p.Ile1180=) c.534A>T (p.Ile178=) n.4001A>T c.3078A>T (p.Ile1026=) n.4858A>T n.4841A>T | dbSNP |
| 12 | g.45852834_45852836del | CA604811922 | ARID2 | c.4711_4713del (p.Glu1571del) c.920_922del c.4632_4634del c.4264_4266del (p.Glu1422del) c.3541_3543del (p.Glu1181del) c.535_537del (p.Glu179del) n.4002_4004del c.3079_3081del (p.Glu1027del) n.4859_4861del n.4842_4844del | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852834del | CA2618443423 | ARID2 | c.4711del (p.Glu1571LysfsTer?) c.920del c.4632del c.4264del (p.Glu1422LysfsTer?) c.3541del (p.Glu1181LysfsTer?) c.535del (p.Glu179LysfsTer?) n.4002del c.3079del (p.Glu1027LysfsTer?) n.4859del n.4842del | gnomAD v4 |
| 12 | g.45852834G>A | CA384492446 | ARID2 | c.4711G>A (p.Glu1571Lys) c.920G>A c.4632G>A c.4264G>A (p.Glu1422Lys) c.3541G>A (p.Glu1181Lys) c.535G>A (p.Glu179Lys) n.4002G>A c.3079G>A (p.Glu1027Lys) n.4859G>A n.4842G>A | dbSNP |
| 12 | g.45852834G>C | CA384492450 | ARID2 | c.4711G>C (p.Glu1571Gln) c.920G>C c.4632G>C c.4264G>C (p.Glu1422Gln) c.3541G>C (p.Glu1181Gln) c.535G>C (p.Glu179Gln) n.4002G>C c.3079G>C (p.Glu1027Gln) n.4859G>C n.4842G>C | dbSNP gnomAD v4 |
| 12 | g.45852834G= | CA2033475789 | ARID2 | c.4711G= (p.Glu1571=) c.920G= c.4632G= c.4264G= (p.Glu1422=) c.3541G= (p.Glu1181=) c.535G= (p.Glu179=) n.4002G= c.3079G= (p.Glu1027=) n.4859G= n.4842G= | |
| 12 | g.45852834G>T | CA384492448 | ARID2 | c.4711G>T (p.Glu1571Ter) c.920G>T c.4632G>T c.4264G>T (p.Glu1422Ter) c.3541G>T (p.Glu1181Ter) c.535G>T (p.Glu179Ter) n.4002G>T c.3079G>T (p.Glu1027Ter) n.4859G>T n.4842G>T | |
| 12 | g.45852835A= | CA2033475790 | ARID2 | c.4712A= (p.Glu1571=) c.921A= c.4633A= c.4265A= (p.Glu1422=) c.3542A= (p.Glu1181=) c.536A= (p.Glu179=) n.4003A= c.3080A= (p.Glu1027=) n.4860A= n.4843A= | |
| 12 | g.45852835A>C | CA384492454 | ARID2 | c.4712A>C (p.Glu1571Ala) c.921A>C c.4633A>C c.4265A>C (p.Glu1422Ala) c.3542A>C (p.Glu1181Ala) c.536A>C (p.Glu179Ala) n.4003A>C c.3080A>C (p.Glu1027Ala) n.4860A>C n.4843A>C | |
| 12 | g.45852835A>G | CA384492456 | ARID2 | c.4712A>G (p.Glu1571Gly) c.921A>G c.4633A>G c.4265A>G (p.Glu1422Gly) c.3542A>G (p.Glu1181Gly) c.536A>G (p.Glu179Gly) n.4003A>G c.3080A>G (p.Glu1027Gly) n.4860A>G n.4843A>G | COSMIC |
| 12 | g.45852835A>T | CA384492458 | ARID2 | c.4712A>T (p.Glu1571Val) c.921A>T c.4633A>T c.4265A>T (p.Glu1422Val) c.3542A>T (p.Glu1181Val) c.536A>T (p.Glu179Val) n.4003A>T c.3080A>T (p.Glu1027Val) n.4860A>T n.4843A>T | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852836A>C | CA384492461 | ARID2 | c.4713A>C (p.Glu1571Asp) c.922A>C c.4634A>C c.4266A>C (p.Glu1422Asp) c.3543A>C (p.Glu1181Asp) c.537A>C (p.Glu179Asp) n.4004A>C c.3081A>C (p.Glu1027Asp) n.4861A>C n.4844A>C | |
| 12 | g.45852836A>G | CA479694236 | ARID2 | c.4713A>G (p.Glu1571=) c.922A>G c.4634A>G c.4266A>G (p.Glu1422=) c.3543A>G (p.Glu1181=) c.537A>G (p.Glu179=) n.4004A>G c.3081A>G (p.Glu1027=) n.4861A>G n.4844A>G | gnomAD v4 |
| 12 | g.45852836A>T | CA384492463 | ARID2 | c.4713A>T (p.Glu1571Asp) c.922A>T c.4634A>T c.4266A>T (p.Glu1422Asp) c.3543A>T (p.Glu1181Asp) c.537A>T (p.Glu179Asp) n.4004A>T c.3081A>T (p.Glu1027Asp) n.4861A>T n.4844A>T | dbSNP |