| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.45852639A>C | CA384491885 | ARID2 | c.4516A>C (p.Thr1506Pro) c.725A>C c.4437A>C c.4069A>C (p.Thr1357Pro) c.3346A>C (p.Thr1116Pro) c.340A>C (p.Thr114Pro) n.3807A>C c.2884A>C (p.Thr962Pro) n.4664A>C n.4647A>C | dbSNP |
| 12 | g.45852639A>G | CA384491886 | ARID2 | c.4516A>G (p.Thr1506Ala) c.725A>G c.4437A>G c.4069A>G (p.Thr1357Ala) c.3346A>G (p.Thr1116Ala) c.340A>G (p.Thr114Ala) n.3807A>G c.2884A>G (p.Thr962Ala) n.4664A>G n.4647A>G | dbSNP gnomAD v4 |
| 12 | g.45852639A>T | CA384491887 | ARID2 | c.4516A>T (p.Thr1506Ser) c.725A>T c.4437A>T c.4069A>T (p.Thr1357Ser) c.3346A>T (p.Thr1116Ser) c.340A>T (p.Thr114Ser) n.3807A>T c.2884A>T (p.Thr962Ser) n.4664A>T n.4647A>T | dbSNP |
| 12 | g.45852640C>A | CA384491888 | ARID2 | c.4517C>A (p.Thr1506Lys) c.726C>A c.4438C>A c.4070C>A (p.Thr1357Lys) c.3347C>A (p.Thr1116Lys) c.341C>A (p.Thr114Lys) n.3808C>A c.2885C>A (p.Thr962Lys) n.4665C>A n.4648C>A | |
| 12 | g.45852640C= | CA2033475714 | ARID2 | c.4517C= (p.Thr1506=) c.726C= c.4438C= c.4070C= (p.Thr1357=) c.3347C= (p.Thr1116=) c.341C= (p.Thr114=) n.3808C= c.2885C= (p.Thr962=) n.4665C= n.4648C= | |
| 12 | g.45852640C>G | CA384491890 | ARID2 | c.4517C>G (p.Thr1506Arg) c.726C>G c.4438C>G c.4070C>G (p.Thr1357Arg) c.3347C>G (p.Thr1116Arg) c.341C>G (p.Thr114Arg) n.3808C>G c.2885C>G (p.Thr962Arg) n.4665C>G n.4648C>G | |
| 12 | g.45852640C>T | CA384491889 | ARID2 | c.4517C>T (p.Thr1506Ile) c.726C>T c.4438C>T c.4070C>T (p.Thr1357Ile) c.3347C>T (p.Thr1116Ile) c.341C>T (p.Thr114Ile) n.3808C>T c.2885C>T (p.Thr962Ile) n.4665C>T n.4648C>T | |
| 12 | g.45852641A>C | CA479693881 | ARID2 | c.4518A>C (p.Thr1506=) c.727A>C c.4439A>C c.4071A>C (p.Thr1357=) c.3348A>C (p.Thr1116=) c.342A>C (p.Thr114=) n.3809A>C c.2886A>C (p.Thr962=) n.4666A>C n.4649A>C | |
| 12 | g.45852641A>G | CA479693882 | ARID2 | c.4518A>G (p.Thr1506=) c.727A>G c.4439A>G c.4071A>G (p.Thr1357=) c.3348A>G (p.Thr1116=) c.342A>G (p.Thr114=) n.3809A>G c.2886A>G (p.Thr962=) n.4666A>G n.4649A>G | gnomAD v4 |
| 12 | g.45852641A>T | CA479693883 | ARID2 | c.4518A>T (p.Thr1506=) c.727A>T c.4439A>T c.4071A>T (p.Thr1357=) c.3348A>T (p.Thr1116=) c.342A>T (p.Thr114=) n.3809A>T c.2886A>T (p.Thr962=) n.4666A>T n.4649A>T | dbSNP |
| 12 | g.45852643dup | CA236400808 | ARID2 | c.4520dup (p.Asn1507LysfsTer17) c.729dup c.4441dup c.4073dup (p.Asn1358LysfsTer17) c.3350dup (p.Asn1117LysfsTer17) c.344dup (p.Asn115LysfsTer17) n.3811dup c.2888dup (p.Asn963LysfsTer17) n.4668dup n.4651dup | dbSNP |
| 12 | g.45852643del | CA2726049926 | ARID2 | c.4520del (p.Asn1507MetfsTer9) c.729del c.4441del c.4073del (p.Asn1358MetfsTer9) c.3350del (p.Asn1117MetfsTer9) c.344del (p.Asn115MetfsTer9) n.3811del c.2888del (p.Asn963MetfsTer9) n.4668del n.4651del | dbSNP |
| 12 | g.45852642A= | CA2033475715 | ARID2 | c.4519A= (p.Asn1507=) c.728A= c.4440A= c.4072A= (p.Asn1358=) c.3349A= (p.Asn1117=) c.343A= (p.Asn115=) n.3810A= c.2887A= (p.Asn963=) n.4667A= n.4650A= | |
| 12 | g.45852642A>C | CA384491891 | ARID2 | c.4519A>C (p.Asn1507His) c.728A>C c.4440A>C c.4072A>C (p.Asn1358His) c.3349A>C (p.Asn1117His) c.343A>C (p.Asn115His) n.3810A>C c.2887A>C (p.Asn963His) n.4667A>C n.4650A>C | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852642A>G | CA6526681 | ARID2 | c.4519A>G (p.Asn1507Asp) c.728A>G c.4440A>G c.4072A>G (p.Asn1358Asp) c.3349A>G (p.Asn1117Asp) c.343A>G (p.Asn115Asp) n.3810A>G c.2887A>G (p.Asn963Asp) n.4667A>G n.4650A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852642A>T | CA384491892 | ARID2 | c.4519A>T (p.Asn1507Tyr) c.728A>T c.4440A>T c.4072A>T (p.Asn1358Tyr) c.3349A>T (p.Asn1117Tyr) c.343A>T (p.Asn115Tyr) n.3810A>T c.2887A>T (p.Asn963Tyr) n.4667A>T n.4650A>T | dbSNP |
| 12 | g.45852643A>C | CA384491893 | ARID2 | c.4520A>C (p.Asn1507Thr) c.729A>C c.4441A>C c.4073A>C (p.Asn1358Thr) c.3350A>C (p.Asn1117Thr) c.344A>C (p.Asn115Thr) n.3811A>C c.2888A>C (p.Asn963Thr) n.4668A>C n.4651A>C | |
| 12 | g.45852643A>G | CA384491894 | ARID2 | c.4520A>G (p.Asn1507Ser) c.729A>G c.4441A>G c.4073A>G (p.Asn1358Ser) c.3350A>G (p.Asn1117Ser) c.344A>G (p.Asn115Ser) n.3811A>G c.2888A>G (p.Asn963Ser) n.4668A>G n.4651A>G | dbSNP gnomAD v4 |
| 12 | g.45852643A>T | CA384491895 | ARID2 | c.4520A>T (p.Asn1507Ile) c.729A>T c.4441A>T c.4073A>T (p.Asn1358Ile) c.3350A>T (p.Asn1117Ile) c.344A>T (p.Asn115Ile) n.3811A>T c.2888A>T (p.Asn963Ile) n.4668A>T n.4651A>T | dbSNP |
| 12 | g.45852644T>A | CA384491896 | ARID2 | c.4521T>A (p.Asn1507Lys) c.730T>A c.4442T>A c.4074T>A (p.Asn1358Lys) c.3351T>A (p.Asn1117Lys) c.345T>A (p.Asn115Lys) n.3812T>A c.2889T>A (p.Asn963Lys) n.4669T>A n.4652T>A | |
| 12 | g.45852644T>C | CA479693884 | ARID2 | c.4521T>C (p.Asn1507=) c.730T>C c.4442T>C c.4074T>C (p.Asn1358=) c.3351T>C (p.Asn1117=) c.345T>C (p.Asn115=) n.3812T>C c.2889T>C (p.Asn963=) n.4669T>C n.4652T>C | |
| 12 | g.45852644T>G | CA384491897 | ARID2 | c.4521T>G (p.Asn1507Lys) c.730T>G c.4442T>G c.4074T>G (p.Asn1358Lys) c.3351T>G (p.Asn1117Lys) c.345T>G (p.Asn115Lys) n.3812T>G c.2889T>G (p.Asn963Lys) n.4669T>G n.4652T>G | dbSNP |
| 12 | g.45852645G>A | CA384491898 | ARID2 | c.4522G>A (p.Gly1508Ser) c.731G>A c.4443G>A c.4075G>A (p.Gly1359Ser) c.3352G>A (p.Gly1118Ser) c.346G>A (p.Gly116Ser) n.3813G>A c.2890G>A (p.Gly964Ser) n.4670G>A n.4653G>A | dbSNP |
| 12 | g.45852645G>C | CA384491899 | ARID2 | c.4522G>C (p.Gly1508Arg) c.731G>C c.4443G>C c.4075G>C (p.Gly1359Arg) c.3352G>C (p.Gly1118Arg) c.346G>C (p.Gly116Arg) n.3813G>C c.2890G>C (p.Gly964Arg) n.4670G>C n.4653G>C | dbSNP |
| 12 | g.45852645G>T | CA384491900 | ARID2 | c.4522G>T (p.Gly1508Cys) c.731G>T c.4443G>T c.4075G>T (p.Gly1359Cys) c.3352G>T (p.Gly1118Cys) c.346G>T (p.Gly116Cys) n.3813G>T c.2890G>T (p.Gly964Cys) n.4670G>T n.4653G>T | dbSNP |
| 12 | g.45852646del | CA2618443261 | ARID2 | c.4523del (p.Gly1508AlafsTer8) c.732del c.4444del c.4076del (p.Gly1359AlafsTer8) c.3353del (p.Gly1118AlafsTer8) c.347del (p.Gly116AlafsTer8) n.3814del c.2891del (p.Gly964AlafsTer8) n.4671del n.4654del | gnomAD v4 |
| 12 | g.45852646G>A | CA384491901 | ARID2 | c.4523G>A (p.Gly1508Asp) c.732G>A c.4444G>A c.4076G>A (p.Gly1359Asp) c.3353G>A (p.Gly1118Asp) c.347G>A (p.Gly116Asp) n.3814G>A c.2891G>A (p.Gly964Asp) n.4671G>A n.4654G>A | dbSNP |
| 12 | g.45852646G>C | CA384491903 | ARID2 | c.4523G>C (p.Gly1508Ala) c.732G>C c.4444G>C c.4076G>C (p.Gly1359Ala) c.3353G>C (p.Gly1118Ala) c.347G>C (p.Gly116Ala) n.3814G>C c.2891G>C (p.Gly964Ala) n.4671G>C n.4654G>C | dbSNP |
| 12 | g.45852646G>T | CA384491902 | ARID2 | c.4523G>T (p.Gly1508Val) c.732G>T c.4444G>T c.4076G>T (p.Gly1359Val) c.3353G>T (p.Gly1118Val) c.347G>T (p.Gly116Val) n.3814G>T c.2891G>T (p.Gly964Val) n.4671G>T n.4654G>T | dbSNP |
| 12 | g.45852647C>A | CA479693885 | ARID2 | c.4524C>A (p.Gly1508=) c.733C>A c.4445C>A c.4077C>A (p.Gly1359=) c.3354C>A (p.Gly1118=) c.348C>A (p.Gly116=) n.3815C>A c.2892C>A (p.Gly964=) n.4672C>A n.4655C>A | dbSNP |
| 12 | g.45852647C= | CA2033475716 | ARID2 | c.4524C= (p.Gly1508=) c.733C= c.4445C= c.4077C= (p.Gly1359=) c.3354C= (p.Gly1118=) c.348C= (p.Gly116=) n.3815C= c.2892C= (p.Gly964=) n.4672C= n.4655C= | |
| 12 | g.45852647C>G | CA479693886 | ARID2 | c.4524C>G (p.Gly1508=) c.733C>G c.4445C>G c.4077C>G (p.Gly1359=) c.3354C>G (p.Gly1118=) c.348C>G (p.Gly116=) n.3815C>G c.2892C>G (p.Gly964=) n.4672C>G n.4655C>G | dbSNP |
| 12 | g.45852647C>T | CA236400818 | ARID2 | c.4524C>T (p.Gly1508=) c.733C>T c.4445C>T c.4077C>T (p.Gly1359=) c.3354C>T (p.Gly1118=) c.348C>T (p.Gly116=) n.3815C>T c.2892C>T (p.Gly964=) n.4672C>T n.4655C>T | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852648A>C | CA384491904 | ARID2 | c.4525A>C (p.Thr1509Pro) c.734A>C c.4446A>C c.4078A>C (p.Thr1360Pro) c.3355A>C (p.Thr1119Pro) c.349A>C (p.Thr117Pro) n.3816A>C c.2893A>C (p.Thr965Pro) n.4673A>C n.4656A>C | dbSNP |
| 12 | g.45852648A>G | CA384491905 | ARID2 | c.4525A>G (p.Thr1509Ala) c.734A>G c.4446A>G c.4078A>G (p.Thr1360Ala) c.3355A>G (p.Thr1119Ala) c.349A>G (p.Thr117Ala) n.3816A>G c.2893A>G (p.Thr965Ala) n.4673A>G n.4656A>G | dbSNP |
| 12 | g.45852648A>T | CA384491906 | ARID2 | c.4525A>T (p.Thr1509Ser) c.734A>T c.4446A>T c.4078A>T (p.Thr1360Ser) c.3355A>T (p.Thr1119Ser) c.349A>T (p.Thr117Ser) n.3816A>T c.2893A>T (p.Thr965Ser) n.4673A>T n.4656A>T | dbSNP |
| 12 | g.45852649C>A | CA384491907 | ARID2 | c.4526C>A (p.Thr1509Lys) c.735C>A c.4447C>A c.4079C>A (p.Thr1360Lys) c.3356C>A (p.Thr1119Lys) c.350C>A (p.Thr117Lys) n.3817C>A c.2894C>A (p.Thr965Lys) n.4674C>A n.4657C>A | dbSNP |
| 12 | g.45852649C= | CA2033475717 | ARID2 | c.4526C= (p.Thr1509=) c.735C= c.4447C= c.4079C= (p.Thr1360=) c.3356C= (p.Thr1119=) c.350C= (p.Thr117=) n.3817C= c.2894C= (p.Thr965=) n.4674C= n.4657C= | |
| 12 | g.45852649C>G | CA384491908 | ARID2 | c.4526C>G (p.Thr1509Arg) c.735C>G c.4447C>G c.4079C>G (p.Thr1360Arg) c.3356C>G (p.Thr1119Arg) c.350C>G (p.Thr117Arg) n.3817C>G c.2894C>G (p.Thr965Arg) n.4674C>G n.4657C>G | dbSNP |
| 12 | g.45852649C>T | CA384491909 | ARID2 | c.4526C>T (p.Thr1509Ile) c.735C>T c.4447C>T c.4079C>T (p.Thr1360Ile) c.3356C>T (p.Thr1119Ile) c.350C>T (p.Thr117Ile) n.3817C>T c.2894C>T (p.Thr965Ile) n.4674C>T n.4657C>T | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852650A>C | CA479693887 | ARID2 | c.4527A>C (p.Thr1509=) c.736A>C c.4448A>C c.4080A>C (p.Thr1360=) c.3357A>C (p.Thr1119=) c.351A>C (p.Thr117=) n.3818A>C c.2895A>C (p.Thr965=) n.4675A>C n.4658A>C | |
| 12 | g.45852650A>G | CA479693888 | ARID2 | c.4527A>G (p.Thr1509=) c.736A>G c.4448A>G c.4080A>G (p.Thr1360=) c.3357A>G (p.Thr1119=) c.351A>G (p.Thr117=) n.3818A>G c.2895A>G (p.Thr965=) n.4675A>G n.4658A>G | dbSNP |
| 12 | g.45852650A>T | CA479693889 | ARID2 | c.4527A>T (p.Thr1509=) c.736A>T c.4448A>T c.4080A>T (p.Thr1360=) c.3357A>T (p.Thr1119=) c.351A>T (p.Thr117=) n.3818A>T c.2895A>T (p.Thr965=) n.4675A>T n.4658A>T | dbSNP |
| 12 | g.45852651G>A | CA384491910 | ARID2 | c.4528G>A (p.Ala1510Thr) c.737G>A c.4449G>A c.4081G>A (p.Ala1361Thr) c.3358G>A (p.Ala1120Thr) c.352G>A (p.Ala118Thr) n.3819G>A c.2896G>A (p.Ala966Thr) n.4676G>A n.4659G>A | dbSNP |
| 12 | g.45852651G>C | CA384491911 | ARID2 | c.4528G>C (p.Ala1510Pro) c.737G>C c.4449G>C c.4081G>C (p.Ala1361Pro) c.3358G>C (p.Ala1120Pro) c.352G>C (p.Ala118Pro) n.3819G>C c.2896G>C (p.Ala966Pro) n.4676G>C n.4659G>C | dbSNP |
| 12 | g.45852651G>T | CA384491912 | ARID2 | c.4528G>T (p.Ala1510Ser) c.737G>T c.4449G>T c.4081G>T (p.Ala1361Ser) c.3358G>T (p.Ala1120Ser) c.352G>T (p.Ala118Ser) n.3819G>T c.2896G>T (p.Ala966Ser) n.4676G>T n.4659G>T | dbSNP |
| 12 | g.45852652C>A | CA384491913 | ARID2 | c.4529C>A (p.Ala1510Glu) c.738C>A c.4450C>A c.4082C>A (p.Ala1361Glu) c.3359C>A (p.Ala1120Glu) c.353C>A (p.Ala118Glu) n.3820C>A c.2897C>A (p.Ala966Glu) n.4677C>A n.4660C>A | dbSNP |
| 12 | g.45852652C= | CA2033475718 | ARID2 | c.4529C= (p.Ala1510=) c.738C= c.4450C= c.4082C= (p.Ala1361=) c.3359C= (p.Ala1120=) c.353C= (p.Ala118=) n.3820C= c.2897C= (p.Ala966=) n.4677C= n.4660C= | |
| 12 | g.45852652C>G | CA384491914 | ARID2 | c.4529C>G (p.Ala1510Gly) c.738C>G c.4450C>G c.4082C>G (p.Ala1361Gly) c.3359C>G (p.Ala1120Gly) c.353C>G (p.Ala118Gly) n.3820C>G c.2897C>G (p.Ala966Gly) n.4677C>G n.4660C>G | dbSNP |
| 12 | g.45852652C>T | CA384491915 | ARID2 | c.4529C>T (p.Ala1510Val) c.738C>T c.4450C>T c.4082C>T (p.Ala1361Val) c.3359C>T (p.Ala1120Val) c.353C>T (p.Ala118Val) n.3820C>T c.2897C>T (p.Ala966Val) n.4677C>T n.4660C>T | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852653A>C | CA479693890 | ARID2 | c.4530A>C (p.Ala1510=) c.739A>C c.4451A>C c.4083A>C (p.Ala1361=) c.3360A>C (p.Ala1120=) c.354A>C (p.Ala118=) n.3821A>C c.2898A>C (p.Ala966=) n.4678A>C n.4661A>C | |
| 12 | g.45852653A>G | CA479693891 | ARID2 | c.4530A>G (p.Ala1510=) c.739A>G c.4451A>G c.4083A>G (p.Ala1361=) c.3360A>G (p.Ala1120=) c.354A>G (p.Ala118=) n.3821A>G c.2898A>G (p.Ala966=) n.4678A>G n.4661A>G | gnomAD v4 |
| 12 | g.45852653A>T | CA479693892 | ARID2 | c.4530A>T (p.Ala1510=) c.739A>T c.4451A>T c.4083A>T (p.Ala1361=) c.3360A>T (p.Ala1120=) c.354A>T (p.Ala118=) n.3821A>T c.2898A>T (p.Ala966=) n.4678A>T n.4661A>T | dbSNP |
| 12 | g.45852654G>A | CA384491917 | ARID2 | c.4531G>A (p.Glu1511Lys) c.740G>A c.4452G>A c.4084G>A (p.Glu1362Lys) c.3361G>A (p.Glu1121Lys) c.355G>A (p.Glu119Lys) n.3822G>A c.2899G>A (p.Glu967Lys) n.4679G>A n.4662G>A | |
| 12 | g.45852654G>C | CA384491918 | ARID2 | c.4531G>C (p.Glu1511Gln) c.740G>C c.4452G>C c.4084G>C (p.Glu1362Gln) c.3361G>C (p.Glu1121Gln) c.355G>C (p.Glu119Gln) n.3822G>C c.2899G>C (p.Glu967Gln) n.4679G>C n.4662G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852654G= | CA2033475719 | ARID2 | c.4531G= (p.Glu1511=) c.740G= c.4452G= c.4084G= (p.Glu1362=) c.3361G= (p.Glu1121=) c.355G= (p.Glu119=) n.3822G= c.2899G= (p.Glu967=) n.4679G= n.4662G= | |
| 12 | g.45852654G>T | CA384491916 | ARID2 | c.4531G>T (p.Glu1511Ter) c.740G>T c.4452G>T c.4084G>T (p.Glu1362Ter) c.3361G>T (p.Glu1121Ter) c.355G>T (p.Glu119Ter) n.3822G>T c.2899G>T (p.Glu967Ter) n.4679G>T n.4662G>T | COSMIC |
| 12 | g.45852655A= | CA2033475720 | ARID2 | c.4532A= (p.Glu1511=) c.741A= c.4453A= c.4085A= (p.Glu1362=) c.3362A= (p.Glu1121=) c.356A= (p.Glu119=) n.3823A= c.2900A= (p.Glu967=) n.4680A= n.4663A= | |
| 12 | g.45852655A>C | CA384491919 | ARID2 | c.4532A>C (p.Glu1511Ala) c.741A>C c.4453A>C c.4085A>C (p.Glu1362Ala) c.3362A>C (p.Glu1121Ala) c.356A>C (p.Glu119Ala) n.3823A>C c.2900A>C (p.Glu967Ala) n.4680A>C n.4663A>C | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852655A>G | CA384491920 | ARID2 | c.4532A>G (p.Glu1511Gly) c.741A>G c.4453A>G c.4085A>G (p.Glu1362Gly) c.3362A>G (p.Glu1121Gly) c.356A>G (p.Glu119Gly) n.3823A>G c.2900A>G (p.Glu967Gly) n.4680A>G n.4663A>G | dbSNP gnomAD v4 |
| 12 | g.45852655A>T | CA384491921 | ARID2 | c.4532A>T (p.Glu1511Val) c.741A>T c.4453A>T c.4085A>T (p.Glu1362Val) c.3362A>T (p.Glu1121Val) c.356A>T (p.Glu119Val) n.3823A>T c.2900A>T (p.Glu967Val) n.4680A>T n.4663A>T | dbSNP |
| 12 | g.45852656del | CA645571101 | ARID2 | c.4533del (p.Glu1511AspfsTer5) c.742del c.4454del c.4086del (p.Glu1362AspfsTer5) c.3363del (p.Glu1121AspfsTer5) c.357del (p.Glu119AspfsTer5) n.3824del c.2901del (p.Glu967AspfsTer5) n.4681del n.4664del | COSMIC COSMIC |
| 12 | g.45852656A>C | CA384491922 | ARID2 | c.4533A>C (p.Glu1511Asp) c.742A>C c.4454A>C c.4086A>C (p.Glu1362Asp) c.3363A>C (p.Glu1121Asp) c.357A>C (p.Glu119Asp) n.3824A>C c.2901A>C (p.Glu967Asp) n.4681A>C n.4664A>C | |
| 12 | g.45852656A>G | CA479694075 | ARID2 | c.4533A>G (p.Glu1511=) c.742A>G c.4454A>G c.4086A>G (p.Glu1362=) c.3363A>G (p.Glu1121=) c.357A>G (p.Glu119=) n.3824A>G c.2901A>G (p.Glu967=) n.4681A>G n.4664A>G | |
| 12 | g.45852656A>T | CA384491923 | ARID2 | c.4533A>T (p.Glu1511Asp) c.742A>T c.4454A>T c.4086A>T (p.Glu1362Asp) c.3363A>T (p.Glu1121Asp) c.357A>T (p.Glu119Asp) n.3824A>T c.2901A>T (p.Glu967Asp) n.4681A>T n.4664A>T | dbSNP gnomAD v4 |
| 12 | g.45852657T>A | CA384491925 | ARID2 | c.4534T>A (p.Cys1512Ser) c.743T>A c.4455T>A c.4087T>A (p.Cys1363Ser) c.3364T>A (p.Cys1122Ser) c.358T>A (p.Cys120Ser) n.3825T>A c.2902T>A (p.Cys968Ser) n.4682T>A n.4665T>A | dbSNP |
| 12 | g.45852657T>C | CA6526682 | ARID2 | c.4534T>C (p.Cys1512Arg) c.743T>C c.4455T>C c.4087T>C (p.Cys1363Arg) c.3364T>C (p.Cys1122Arg) c.358T>C (p.Cys120Arg) n.3825T>C c.2902T>C (p.Cys968Arg) n.4682T>C n.4665T>C | dbSNP ExAC gnomAD v2 |
| 12 | g.45852657T>G | CA384491924 | ARID2 | c.4534T>G (p.Cys1512Gly) c.743T>G c.4455T>G c.4087T>G (p.Cys1363Gly) c.3364T>G (p.Cys1122Gly) c.358T>G (p.Cys120Gly) n.3825T>G c.2902T>G (p.Cys968Gly) n.4682T>G n.4665T>G | ClinVar dbSNP |
| 12 | g.45852657T= | CA2033475721 | ARID2 | c.4534T= (p.Cys1512=) c.743T= c.4455T= c.4087T= (p.Cys1363=) c.3364T= (p.Cys1122=) c.358T= (p.Cys120=) n.3825T= c.2902T= (p.Cys968=) n.4682T= n.4665T= | |
| 12 | g.45852658G>A | CA384491926 | ARID2 | c.4535G>A (p.Cys1512Tyr) c.744G>A c.4456G>A c.4088G>A (p.Cys1363Tyr) c.3365G>A (p.Cys1122Tyr) c.359G>A (p.Cys120Tyr) n.3826G>A c.2903G>A (p.Cys968Tyr) n.4683G>A n.4666G>A | |
| 12 | g.45852658G>C | CA384491927 | ARID2 | c.4535G>C (p.Cys1512Ser) c.744G>C c.4456G>C c.4088G>C (p.Cys1363Ser) c.3365G>C (p.Cys1122Ser) c.359G>C (p.Cys120Ser) n.3826G>C c.2903G>C (p.Cys968Ser) n.4683G>C n.4666G>C | dbSNP |
| 12 | g.45852658G>T | CA384491928 | ARID2 | c.4535G>T (p.Cys1512Phe) c.744G>T c.4456G>T c.4088G>T (p.Cys1363Phe) c.3365G>T (p.Cys1122Phe) c.359G>T (p.Cys120Phe) n.3826G>T c.2903G>T (p.Cys968Phe) n.4683G>T n.4666G>T | |
| 12 | g.45852658_45852668del | CA645571102 | ARID2 | c.4535_4545del (p.Cys1512Ter) c.744_754del c.4456_4466del c.4088_4098del (p.Cys1363Ter) c.3365_3375del (p.Cys1122Ter) c.359_369del (p.Cys120Ter) n.3826_3836del c.2903_2913del (p.Cys968Ter) n.4683_4693del n.4666_4676del | COSMIC |
| 12 | g.45852659C>A | CA384491929 | ARID2 | c.4536C>A (p.Cys1512Ter) c.745C>A c.4457C>A c.4089C>A (p.Cys1363Ter) c.3366C>A (p.Cys1122Ter) c.360C>A (p.Cys120Ter) n.3827C>A c.2904C>A (p.Cys968Ter) n.4684C>A n.4667C>A | |
| 12 | g.45852659C>G | CA384491930 | ARID2 | c.4536C>G (p.Cys1512Trp) c.745C>G c.4457C>G c.4089C>G (p.Cys1363Trp) c.3366C>G (p.Cys1122Trp) c.360C>G (p.Cys120Trp) n.3827C>G c.2904C>G (p.Cys968Trp) n.4684C>G n.4667C>G | |
| 12 | g.45852659C>T | CA479694076 | ARID2 | c.4536C>T (p.Cys1512=) c.745C>T c.4457C>T c.4089C>T (p.Cys1363=) c.3366C>T (p.Cys1122=) c.360C>T (p.Cys120=) n.3827C>T c.2904C>T (p.Cys968=) n.4684C>T n.4667C>T | |
| 12 | g.45852660A>C | CA384491931 | ARID2 | c.4537A>C (p.Lys1513Gln) c.746A>C c.4458A>C c.4090A>C (p.Lys1364Gln) c.3367A>C (p.Lys1123Gln) c.361A>C (p.Lys121Gln) n.3828A>C c.2905A>C (p.Lys969Gln) n.4685A>C n.4668A>C | |
| 12 | g.45852660A>G | CA384491933 | ARID2 | c.4537A>G (p.Lys1513Glu) c.746A>G c.4458A>G c.4090A>G (p.Lys1364Glu) c.3367A>G (p.Lys1123Glu) c.361A>G (p.Lys121Glu) n.3828A>G c.2905A>G (p.Lys969Glu) n.4685A>G n.4668A>G | dbSNP |
| 12 | g.45852660A>T | CA384491932 | ARID2 | c.4537A>T (p.Lys1513Ter) c.746A>T c.4458A>T c.4090A>T (p.Lys1364Ter) c.3367A>T (p.Lys1123Ter) c.361A>T (p.Lys121Ter) n.3828A>T c.2905A>T (p.Lys969Ter) n.4685A>T n.4668A>T | dbSNP |
| 12 | g.45852661A= | CA2033475722 | ARID2 | c.4538A= (p.Lys1513=) c.747A= c.4459A= c.4091A= (p.Lys1364=) c.3368A= (p.Lys1123=) c.362A= (p.Lys121=) n.3829A= c.2906A= (p.Lys969=) n.4686A= n.4669A= | |
| 12 | g.45852661A>C | CA384491934 | ARID2 | c.4538A>C (p.Lys1513Thr) c.747A>C c.4459A>C c.4091A>C (p.Lys1364Thr) c.3368A>C (p.Lys1123Thr) c.362A>C (p.Lys121Thr) n.3829A>C c.2906A>C (p.Lys969Thr) n.4686A>C n.4669A>C | |
| 12 | g.45852661A>G | CA384491936 | ARID2 | c.4538A>G (p.Lys1513Arg) c.747A>G c.4459A>G c.4091A>G (p.Lys1364Arg) c.3368A>G (p.Lys1123Arg) c.362A>G (p.Lys121Arg) n.3829A>G c.2906A>G (p.Lys969Arg) n.4686A>G n.4669A>G | ClinVar dbSNP gnomAD v4 |
| 12 | g.45852661A>T | CA384491935 | ARID2 | c.4538A>T (p.Lys1513Ile) c.747A>T c.4459A>T c.4091A>T (p.Lys1364Ile) c.3368A>T (p.Lys1123Ile) c.362A>T (p.Lys121Ile) n.3829A>T c.2906A>T (p.Lys969Ile) n.4686A>T n.4669A>T | dbSNP |
| 12 | g.45852662A>C | CA384491937 | ARID2 | c.4539A>C (p.Lys1513Asn) c.748A>C c.4460A>C c.4092A>C (p.Lys1364Asn) c.3369A>C (p.Lys1123Asn) c.363A>C (p.Lys121Asn) n.3830A>C c.2907A>C (p.Lys969Asn) n.4687A>C n.4670A>C | |
| 12 | g.45852662A>G | CA479694077 | ARID2 | c.4539A>G (p.Lys1513=) c.748A>G c.4460A>G c.4092A>G (p.Lys1364=) c.3369A>G (p.Lys1123=) c.363A>G (p.Lys121=) n.3830A>G c.2907A>G (p.Lys969=) n.4687A>G n.4670A>G | |
| 12 | g.45852662A>T | CA384491938 | ARID2 | c.4539A>T (p.Lys1513Asn) c.748A>T c.4460A>T c.4092A>T (p.Lys1364Asn) c.3369A>T (p.Lys1123Asn) c.363A>T (p.Lys121Asn) n.3830A>T c.2907A>T (p.Lys969Asn) n.4687A>T n.4670A>T | dbSNP |
| 12 | g.45852663A= | CA2033475723 | ARID2 | c.4540A= (p.Thr1514=) c.749A= c.4461A= c.4093A= (p.Thr1365=) c.3370A= (p.Thr1124=) c.364A= (p.Thr122=) n.3831A= c.2908A= (p.Thr970=) n.4688A= n.4671A= | |
| 12 | g.45852663A>C | CA384491939 | ARID2 | c.4540A>C (p.Thr1514Pro) c.749A>C c.4461A>C c.4093A>C (p.Thr1365Pro) c.3370A>C (p.Thr1124Pro) c.364A>C (p.Thr122Pro) n.3831A>C c.2908A>C (p.Thr970Pro) n.4688A>C n.4671A>C | dbSNP |
| 12 | g.45852663A>G | CA384491940 | ARID2 | c.4540A>G (p.Thr1514Ala) c.749A>G c.4461A>G c.4093A>G (p.Thr1365Ala) c.3370A>G (p.Thr1124Ala) c.364A>G (p.Thr122Ala) n.3831A>G c.2908A>G (p.Thr970Ala) n.4688A>G n.4671A>G | dbSNP gnomAD v4 |
| 12 | g.45852663A>T | CA384491941 | ARID2 | c.4540A>T (p.Thr1514Ser) c.749A>T c.4461A>T c.4093A>T (p.Thr1365Ser) c.3370A>T (p.Thr1124Ser) c.364A>T (p.Thr122Ser) n.3831A>T c.2908A>T (p.Thr970Ser) n.4688A>T n.4671A>T | dbSNP |
| 12 | g.45852663_45852664delinsGAA | CA2499221641 | ARID2 | c.4540_4541delinsGAA (p.Thr1514GlufsTer10) c.749_750delinsGAA c.4461_4462delinsGAA c.4093_4094delinsGAA (p.Thr1365GlufsTer10) c.3370_3371delinsGAA (p.Thr1124GlufsTer10) c.364_365delinsGAA (p.Thr122GlufsTer10) n.3831_3832delinsGAA c.2908_2909delinsGAA (p.Thr970GlufsTer10) n.4688_4689delinsGAA n.4671_4672delinsGAA | ClinVar dbSNP |
| 12 | g.45852664C>A | CA384491942 | ARID2 | c.4541C>A (p.Thr1514Asn) c.750C>A c.4462C>A c.4094C>A (p.Thr1365Asn) c.3371C>A (p.Thr1124Asn) c.365C>A (p.Thr122Asn) n.3832C>A c.2909C>A (p.Thr970Asn) n.4689C>A n.4672C>A | |
| 12 | g.45852664C>G | CA384491943 | ARID2 | c.4541C>G (p.Thr1514Ser) c.750C>G c.4462C>G c.4094C>G (p.Thr1365Ser) c.3371C>G (p.Thr1124Ser) c.365C>G (p.Thr122Ser) n.3832C>G c.2909C>G (p.Thr970Ser) n.4689C>G n.4672C>G | |
| 12 | g.45852664C>T | CA384491944 | ARID2 | c.4541C>T (p.Thr1514Ile) c.750C>T c.4462C>T c.4094C>T (p.Thr1365Ile) c.3371C>T (p.Thr1124Ile) c.365C>T (p.Thr122Ile) n.3832C>T c.2909C>T (p.Thr970Ile) n.4689C>T n.4672C>T | |
| 12 | g.45852665T>A | CA479694079 | ARID2 | c.4542T>A (p.Thr1514=) c.751T>A c.4463T>A c.4095T>A (p.Thr1365=) c.3372T>A (p.Thr1124=) c.366T>A (p.Thr122=) n.3833T>A c.2910T>A (p.Thr970=) n.4690T>A n.4673T>A | |
| 12 | g.45852665T>C | CA479694080 | ARID2 | c.4542T>C (p.Thr1514=) c.751T>C c.4463T>C c.4095T>C (p.Thr1365=) c.3372T>C (p.Thr1124=) c.366T>C (p.Thr122=) n.3833T>C c.2910T>C (p.Thr970=) n.4690T>C n.4673T>C | |
| 12 | g.45852665T>G | CA479694078 | ARID2 | c.4542T>G (p.Thr1514=) c.751T>G c.4463T>G c.4095T>G (p.Thr1365=) c.3372T>G (p.Thr1124=) c.366T>G (p.Thr122=) n.3833T>G c.2910T>G (p.Thr970=) n.4690T>G n.4673T>G | |
| 12 | g.45852666G>A | CA384491945 | ARID2 | c.4543G>A (p.Val1515Ile) c.752G>A c.4464G>A c.4096G>A (p.Val1366Ile) c.3373G>A (p.Val1125Ile) c.367G>A (p.Val123Ile) n.3834G>A c.2911G>A (p.Val971Ile) n.4691G>A n.4674G>A | dbSNP |
| 12 | g.45852666G>C | CA384491946 | ARID2 | c.4543G>C (p.Val1515Leu) c.752G>C c.4464G>C c.4096G>C (p.Val1366Leu) c.3373G>C (p.Val1125Leu) c.367G>C (p.Val123Leu) n.3834G>C c.2911G>C (p.Val971Leu) n.4691G>C n.4674G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852666G= | CA2033475724 | ARID2 | c.4543G= (p.Val1515=) c.752G= c.4464G= c.4096G= (p.Val1366=) c.3373G= (p.Val1125=) c.367G= (p.Val123=) n.3834G= c.2911G= (p.Val971=) n.4691G= n.4674G= | |
| 12 | g.45852666G>T | CA384491947 | ARID2 | c.4543G>T (p.Val1515Leu) c.752G>T c.4464G>T c.4096G>T (p.Val1366Leu) c.3373G>T (p.Val1125Leu) c.367G>T (p.Val123Leu) n.3834G>T c.2911G>T (p.Val971Leu) n.4691G>T n.4674G>T | |
| 12 | g.45852667T>A | CA384491950 | ARID2 | c.4544T>A (p.Val1515Glu) c.753T>A c.4465T>A c.4097T>A (p.Val1366Glu) c.3374T>A (p.Val1125Glu) c.368T>A (p.Val123Glu) n.3835T>A c.2912T>A (p.Val971Glu) n.4692T>A n.4675T>A | |
| 12 | g.45852667T>C | CA384491949 | ARID2 | c.4544T>C (p.Val1515Ala) c.753T>C c.4465T>C c.4097T>C (p.Val1366Ala) c.3374T>C (p.Val1125Ala) c.368T>C (p.Val123Ala) n.3835T>C c.2912T>C (p.Val971Ala) n.4692T>C n.4675T>C | |
| 12 | g.45852667T>G | CA384491948 | ARID2 | c.4544T>G (p.Val1515Gly) c.753T>G c.4465T>G c.4097T>G (p.Val1366Gly) c.3374T>G (p.Val1125Gly) c.368T>G (p.Val123Gly) n.3835T>G c.2912T>G (p.Val971Gly) n.4692T>G n.4675T>G | dbSNP |
| 12 | g.45852668A= | CA2033475725 | ARID2 | c.4545A= (p.Val1515=) c.754A= c.4466A= c.4098A= (p.Val1366=) c.3375A= (p.Val1125=) c.369A= (p.Val123=) n.3836A= c.2913A= (p.Val971=) n.4693A= n.4676A= | |
| 12 | g.45852668A>C | CA479694082 | ARID2 | c.4545A>C (p.Val1515=) c.754A>C c.4466A>C c.4098A>C (p.Val1366=) c.3375A>C (p.Val1125=) c.369A>C (p.Val123=) n.3836A>C c.2913A>C (p.Val971=) n.4693A>C n.4676A>C | |
| 12 | g.45852668A>G | CA6526683 | ARID2 | c.4545A>G (p.Val1515=) c.754A>G c.4466A>G c.4098A>G (p.Val1366=) c.3375A>G (p.Val1125=) c.369A>G (p.Val123=) n.3836A>G c.2913A>G (p.Val971=) n.4693A>G n.4676A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852668A>T | CA479694081 | ARID2 | c.4545A>T (p.Val1515=) c.754A>T c.4466A>T c.4098A>T (p.Val1366=) c.3375A>T (p.Val1125=) c.369A>T (p.Val123=) n.3836A>T c.2913A>T (p.Val971=) n.4693A>T n.4676A>T | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852669A>C | CA384491951 | ARID2 | c.4546A>C (p.Lys1516Gln) c.755A>C c.4467A>C c.4099A>C (p.Lys1367Gln) c.3376A>C (p.Lys1126Gln) c.370A>C (p.Lys124Gln) n.3837A>C c.2914A>C (p.Lys972Gln) n.4694A>C n.4677A>C | |
| 12 | g.45852669A>G | CA384491952 | ARID2 | c.4546A>G (p.Lys1516Glu) c.755A>G c.4467A>G c.4099A>G (p.Lys1367Glu) c.3376A>G (p.Lys1126Glu) c.370A>G (p.Lys124Glu) n.3837A>G c.2914A>G (p.Lys972Glu) n.4694A>G n.4677A>G | dbSNP |
| 12 | g.45852669A>T | CA384491953 | ARID2 | c.4546A>T (p.Lys1516Ter) c.755A>T c.4467A>T c.4099A>T (p.Lys1367Ter) c.3376A>T (p.Lys1126Ter) c.370A>T (p.Lys124Ter) n.3837A>T c.2914A>T (p.Lys972Ter) n.4694A>T n.4677A>T | dbSNP |
| 12 | g.45852670A>C | CA384491954 | ARID2 | c.4547A>C (p.Lys1516Thr) c.756A>C c.4468A>C c.4100A>C (p.Lys1367Thr) c.3377A>C (p.Lys1126Thr) c.371A>C (p.Lys124Thr) n.3838A>C c.2915A>C (p.Lys972Thr) n.4695A>C n.4678A>C | |
| 12 | g.45852670A>G | CA384491955 | ARID2 | c.4547A>G (p.Lys1516Arg) c.756A>G c.4468A>G c.4100A>G (p.Lys1367Arg) c.3377A>G (p.Lys1126Arg) c.371A>G (p.Lys124Arg) n.3838A>G c.2915A>G (p.Lys972Arg) n.4695A>G n.4678A>G | |
| 12 | g.45852670A>T | CA384491956 | ARID2 | c.4547A>T (p.Lys1516Met) c.756A>T c.4468A>T c.4100A>T (p.Lys1367Met) c.3377A>T (p.Lys1126Met) c.371A>T (p.Lys124Met) n.3838A>T c.2915A>T (p.Lys972Met) n.4695A>T n.4678A>T | |
| 12 | g.45852671G>A | CA479694083 | ARID2 | c.4548G>A (p.Lys1516=) c.757G>A c.4469G>A c.4101G>A (p.Lys1367=) c.3378G>A (p.Lys1126=) c.372G>A (p.Lys124=) n.3839G>A c.2916G>A (p.Lys972=) n.4696G>A n.4679G>A | dbSNP gnomAD v4 |
| 12 | g.45852671G>C | CA384491957 | ARID2 | c.4548G>C (p.Lys1516Asn) c.757G>C c.4469G>C c.4101G>C (p.Lys1367Asn) c.3378G>C (p.Lys1126Asn) c.372G>C (p.Lys124Asn) n.3839G>C c.2916G>C (p.Lys972Asn) n.4696G>C n.4679G>C | dbSNP |
| 12 | g.45852671G>T | CA384491958 | ARID2 | c.4548G>T (p.Lys1516Asn) c.757G>T c.4469G>T c.4101G>T (p.Lys1367Asn) c.3378G>T (p.Lys1126Asn) c.372G>T (p.Lys124Asn) n.3839G>T c.2916G>T (p.Lys972Asn) n.4696G>T n.4679G>T | dbSNP |
| 12 | g.45852672A>C | CA479694084 | ARID2 | c.4549A>C (p.Arg1517=) c.758A>C c.4470A>C c.4102A>C (p.Arg1368=) c.3379A>C (p.Arg1127=) c.373A>C (p.Arg125=) n.3840A>C c.2917A>C (p.Arg973=) n.4697A>C n.4680A>C | |
| 12 | g.45852672A>G | CA384491959 | ARID2 | c.4549A>G (p.Arg1517Gly) c.758A>G c.4470A>G c.4102A>G (p.Arg1368Gly) c.3379A>G (p.Arg1127Gly) c.373A>G (p.Arg125Gly) n.3840A>G c.2917A>G (p.Arg973Gly) n.4697A>G n.4680A>G | dbSNP |
| 12 | g.45852672A>T | CA384491960 | ARID2 | c.4549A>T (p.Arg1517Trp) c.758A>T c.4470A>T c.4102A>T (p.Arg1368Trp) c.3379A>T (p.Arg1127Trp) c.373A>T (p.Arg125Trp) n.3840A>T c.2917A>T (p.Arg973Trp) n.4697A>T n.4680A>T | dbSNP |
| 12 | g.45852673G>A | CA384491963 | ARID2 | c.4550G>A (p.Arg1517Lys) c.759G>A c.4471G>A c.4103G>A (p.Arg1368Lys) c.3380G>A (p.Arg1127Lys) c.374G>A (p.Arg125Lys) n.3841G>A c.2918G>A (p.Arg973Lys) n.4698G>A n.4681G>A | dbSNP |
| 12 | g.45852673G>C | CA384491962 | ARID2 | c.4550G>C (p.Arg1517Thr) c.759G>C c.4471G>C c.4103G>C (p.Arg1368Thr) c.3380G>C (p.Arg1127Thr) c.374G>C (p.Arg125Thr) n.3841G>C c.2918G>C (p.Arg973Thr) n.4698G>C n.4681G>C | dbSNP |
| 12 | g.45852673G>T | CA384491961 | ARID2 | c.4550G>T (p.Arg1517Met) c.759G>T c.4471G>T c.4103G>T (p.Arg1368Met) c.3380G>T (p.Arg1127Met) c.374G>T (p.Arg125Met) n.3841G>T c.2918G>T (p.Arg973Met) n.4698G>T n.4681G>T | dbSNP |
| 12 | g.45852674G>A | CA479694085 | ARID2 | c.4551G>A (p.Arg1517=) c.760G>A c.4472G>A c.4104G>A (p.Arg1368=) c.3381G>A (p.Arg1127=) c.375G>A (p.Arg125=) n.3842G>A c.2919G>A (p.Arg973=) n.4699G>A n.4682G>A | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852674G>C | CA384491964 | ARID2 | c.4551G>C (p.Arg1517Ser) c.760G>C c.4472G>C c.4104G>C (p.Arg1368Ser) c.3381G>C (p.Arg1127Ser) c.375G>C (p.Arg125Ser) n.3842G>C c.2919G>C (p.Arg973Ser) n.4699G>C n.4682G>C | |
| 12 | g.45852674G= | CA2033475726 | ARID2 | c.4551G= (p.Arg1517=) c.760G= c.4472G= c.4104G= (p.Arg1368=) c.3381G= (p.Arg1127=) c.375G= (p.Arg125=) n.3842G= c.2919G= (p.Arg973=) n.4699G= n.4682G= | |
| 12 | g.45852674G>T | CA384491965 | ARID2 | c.4551G>T (p.Arg1517Ser) c.760G>T c.4472G>T c.4104G>T (p.Arg1368Ser) c.3381G>T (p.Arg1127Ser) c.375G>T (p.Arg125Ser) n.3842G>T c.2919G>T (p.Arg973Ser) n.4699G>T n.4682G>T | |
| 12 | g.45852675C>A | CA384491966 | ARID2 | c.4552C>A (p.Pro1518Thr) c.761C>A c.4473C>A c.4105C>A (p.Pro1369Thr) c.3382C>A (p.Pro1128Thr) c.376C>A (p.Pro126Thr) n.3843C>A c.2920C>A (p.Pro974Thr) n.4700C>A n.4683C>A | dbSNP |
| 12 | g.45852675C>G | CA384491967 | ARID2 | c.4552C>G (p.Pro1518Ala) c.761C>G c.4473C>G c.4105C>G (p.Pro1369Ala) c.3382C>G (p.Pro1128Ala) c.376C>G (p.Pro126Ala) n.3843C>G c.2920C>G (p.Pro974Ala) n.4700C>G n.4683C>G | dbSNP |
| 12 | g.45852675C>T | CA384491968 | ARID2 | c.4552C>T (p.Pro1518Ser) c.761C>T c.4473C>T c.4105C>T (p.Pro1369Ser) c.3382C>T (p.Pro1128Ser) c.376C>T (p.Pro126Ser) n.3843C>T c.2920C>T (p.Pro974Ser) n.4700C>T n.4683C>T | dbSNP |
| 12 | g.45852676C>A | CA384491970 | ARID2 | c.4553C>A (p.Pro1518Gln) c.762C>A c.4474C>A c.4106C>A (p.Pro1369Gln) c.3383C>A (p.Pro1128Gln) c.377C>A (p.Pro126Gln) n.3844C>A c.2921C>A (p.Pro974Gln) n.4701C>A n.4684C>A | dbSNP |
| 12 | g.45852676C= | CA2033475727 | ARID2 | c.4553C= (p.Pro1518=) c.762C= c.4474C= c.4106C= (p.Pro1369=) c.3383C= (p.Pro1128=) c.377C= (p.Pro126=) n.3844C= c.2921C= (p.Pro974=) n.4701C= n.4684C= | |
| 12 | g.45852676C>G | CA384491969 | ARID2 | c.4553C>G (p.Pro1518Arg) c.762C>G c.4474C>G c.4106C>G (p.Pro1369Arg) c.3383C>G (p.Pro1128Arg) c.377C>G (p.Pro126Arg) n.3844C>G c.2921C>G (p.Pro974Arg) n.4701C>G n.4684C>G | dbSNP |
| 12 | g.45852676C>T | CA6526684 | ARID2 | c.4553C>T (p.Pro1518Leu) c.762C>T c.4474C>T c.4106C>T (p.Pro1369Leu) c.3383C>T (p.Pro1128Leu) c.377C>T (p.Pro126Leu) n.3844C>T c.2921C>T (p.Pro974Leu) n.4701C>T n.4684C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852677A>C | CA479694086 | ARID2 | c.4554A>C (p.Pro1518=) c.763A>C c.4475A>C c.4107A>C (p.Pro1369=) c.3384A>C (p.Pro1128=) c.378A>C (p.Pro126=) n.3845A>C c.2922A>C (p.Pro974=) n.4702A>C n.4685A>C | gnomAD v4 |
| 12 | g.45852677A>G | CA479694087 | ARID2 | c.4554A>G (p.Pro1518=) c.763A>G c.4475A>G c.4107A>G (p.Pro1369=) c.3384A>G (p.Pro1128=) c.378A>G (p.Pro126=) n.3845A>G c.2922A>G (p.Pro974=) n.4702A>G n.4685A>G | gnomAD v4 |
| 12 | g.45852677A>T | CA479694088 | ARID2 | c.4554A>T (p.Pro1518=) c.763A>T c.4475A>T c.4107A>T (p.Pro1369=) c.3384A>T (p.Pro1128=) c.378A>T (p.Pro126=) n.3845A>T c.2922A>T (p.Pro974=) n.4702A>T n.4685A>T | dbSNP |
| 12 | g.45852678G>A | CA236400833 | ARID2 | c.4555G>A (p.Ala1519Thr) c.764G>A c.4476G>A c.4108G>A (p.Ala1370Thr) c.3385G>A (p.Ala1129Thr) c.379G>A (p.Ala127Thr) n.3846G>A c.2923G>A (p.Ala975Thr) n.4703G>A n.4686G>A | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.45852678G>C | CA6526686 | ARID2 | c.4555G>C (p.Ala1519Pro) c.764G>C c.4476G>C c.4108G>C (p.Ala1370Pro) c.3385G>C (p.Ala1129Pro) c.379G>C (p.Ala127Pro) n.3846G>C c.2923G>C (p.Ala975Pro) n.4703G>C n.4686G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.45852678G= | CA2033475728 | ARID2 | c.4555G= (p.Ala1519=) c.764G= c.4476G= c.4108G= (p.Ala1370=) c.3385G= (p.Ala1129=) c.379G= (p.Ala127=) n.3846G= c.2923G= (p.Ala975=) n.4703G= n.4686G= | |
| 12 | g.45852678G>T | CA6526685 | ARID2 | c.4555G>T (p.Ala1519Ser) c.764G>T c.4476G>T c.4108G>T (p.Ala1370Ser) c.3385G>T (p.Ala1129Ser) c.379G>T (p.Ala127Ser) n.3846G>T c.2923G>T (p.Ala975Ser) n.4703G>T n.4686G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852679C>A | CA384491971 | ARID2 | c.4556C>A (p.Ala1519Glu) c.765C>A c.4477C>A c.4109C>A (p.Ala1370Glu) c.3386C>A (p.Ala1129Glu) c.380C>A (p.Ala127Glu) n.3847C>A c.2924C>A (p.Ala975Glu) n.4704C>A n.4687C>A | dbSNP |
| 12 | g.45852679C= | CA2033475729 | ARID2 | c.4556C= (p.Ala1519=) c.765C= c.4477C= c.4109C= (p.Ala1370=) c.3386C= (p.Ala1129=) c.380C= (p.Ala127=) n.3847C= c.2924C= (p.Ala975=) n.4704C= n.4687C= | |
| 12 | g.45852679C>G | CA384491972 | ARID2 | c.4556C>G (p.Ala1519Gly) c.765C>G c.4477C>G c.4109C>G (p.Ala1370Gly) c.3386C>G (p.Ala1129Gly) c.380C>G (p.Ala127Gly) n.3847C>G c.2924C>G (p.Ala975Gly) n.4704C>G n.4687C>G | dbSNP |
| 12 | g.45852679C>T | CA6526687 | ARID2 | c.4556C>T (p.Ala1519Val) c.765C>T c.4477C>T c.4109C>T (p.Ala1370Val) c.3386C>T (p.Ala1129Val) c.380C>T (p.Ala127Val) n.3847C>T c.2924C>T (p.Ala975Val) n.4704C>T n.4687C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.45852680A>C | CA479694089 | ARID2 | c.4557A>C (p.Ala1519=) c.766A>C c.4478A>C c.4110A>C (p.Ala1370=) c.3387A>C (p.Ala1129=) c.381A>C (p.Ala127=) n.3848A>C c.2925A>C (p.Ala975=) n.4705A>C n.4688A>C | |
| 12 | g.45852680A>G | CA479694090 | ARID2 | c.4557A>G (p.Ala1519=) c.766A>G c.4478A>G c.4110A>G (p.Ala1370=) c.3387A>G (p.Ala1129=) c.381A>G (p.Ala127=) n.3848A>G c.2925A>G (p.Ala975=) n.4705A>G n.4688A>G | dbSNP |
| 12 | g.45852680A>T | CA479694091 | ARID2 | c.4557A>T (p.Ala1519=) c.766A>T c.4478A>T c.4110A>T (p.Ala1370=) c.3387A>T (p.Ala1129=) c.381A>T (p.Ala127=) n.3848A>T c.2925A>T (p.Ala975=) n.4705A>T n.4688A>T | |
| 12 | g.45852681G>A | CA384491973 | ARID2 | c.4558G>A (p.Glu1520Lys) c.767G>A c.4479G>A c.4111G>A (p.Glu1371Lys) c.3388G>A (p.Glu1130Lys) c.382G>A (p.Glu128Lys) n.3849G>A c.2926G>A (p.Glu976Lys) n.4706G>A n.4689G>A | dbSNP gnomAD v4 |
| 12 | g.45852681G>C | CA384491975 | ARID2 | c.4558G>C (p.Glu1520Gln) c.767G>C c.4479G>C c.4111G>C (p.Glu1371Gln) c.3388G>C (p.Glu1130Gln) c.382G>C (p.Glu128Gln) n.3849G>C c.2926G>C (p.Glu976Gln) n.4706G>C n.4689G>C | dbSNP |
| 12 | g.45852681G= | CA2033475730 | ARID2 | c.4558G= (p.Glu1520=) c.767G= c.4479G= c.4111G= (p.Glu1371=) c.3388G= (p.Glu1130=) c.382G= (p.Glu128=) n.3849G= c.2926G= (p.Glu976=) n.4706G= n.4689G= | |
| 12 | g.45852681G>T | CA384491974 | ARID2 | c.4558G>T (p.Glu1520Ter) c.767G>T c.4479G>T c.4111G>T (p.Glu1371Ter) c.3388G>T (p.Glu1130Ter) c.382G>T (p.Glu128Ter) n.3849G>T c.2926G>T (p.Glu976Ter) n.4706G>T n.4689G>T | COSMIC |
| 12 | g.45852682A>C | CA384491976 | ARID2 | c.4559A>C (p.Glu1520Ala) c.768A>C c.4480A>C c.4112A>C (p.Glu1371Ala) c.3389A>C (p.Glu1130Ala) c.383A>C (p.Glu128Ala) n.3850A>C c.2927A>C (p.Glu976Ala) n.4707A>C n.4690A>C | |
| 12 | g.45852682A>G | CA384491977 | ARID2 | c.4559A>G (p.Glu1520Gly) c.768A>G c.4480A>G c.4112A>G (p.Glu1371Gly) c.3389A>G (p.Glu1130Gly) c.383A>G (p.Glu128Gly) n.3850A>G c.2927A>G (p.Glu976Gly) n.4707A>G n.4690A>G | dbSNP |
| 12 | g.45852682A>T | CA384491978 | ARID2 | c.4559A>T (p.Glu1520Val) c.768A>T c.4480A>T c.4112A>T (p.Glu1371Val) c.3389A>T (p.Glu1130Val) c.383A>T (p.Glu128Val) n.3850A>T c.2927A>T (p.Glu976Val) n.4707A>T n.4690A>T | dbSNP |
| 12 | g.45852683G>A | CA479694092 | ARID2 | c.4560G>A (p.Glu1520=) c.769G>A c.4481G>A c.4113G>A (p.Glu1371=) c.3390G>A (p.Glu1130=) c.384G>A (p.Glu128=) n.3851G>A c.2928G>A (p.Glu976=) n.4708G>A n.4691G>A | dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.45852683G>C | CA384491979 | ARID2 | c.4560G>C (p.Glu1520Asp) c.769G>C c.4481G>C c.4113G>C (p.Glu1371Asp) c.3390G>C (p.Glu1130Asp) c.384G>C (p.Glu128Asp) n.3851G>C c.2928G>C (p.Glu976Asp) n.4708G>C n.4691G>C | |
| 12 | g.45852683G= | CA2033475731 | ARID2 | c.4560G= (p.Glu1520=) c.769G= c.4481G= c.4113G= (p.Glu1371=) c.3390G= (p.Glu1130=) c.384G= (p.Glu128=) n.3851G= c.2928G= (p.Glu976=) n.4708G= n.4691G= | |
| 12 | g.45852683G>T | CA384491980 | ARID2 | c.4560G>T (p.Glu1520Asp) c.769G>T c.4481G>T c.4113G>T (p.Glu1371Asp) c.3390G>T (p.Glu1130Asp) c.384G>T (p.Glu128Asp) n.3851G>T c.2928G>T (p.Glu976Asp) n.4708G>T n.4691G>T | dbSNP |
| 12 | g.45852684G>A | CA384491981 | ARID2 | c.4561G>A (p.Asp1521Asn) c.770G>A c.4482G>A c.4114G>A (p.Asp1372Asn) c.3391G>A (p.Asp1131Asn) c.385G>A (p.Asp129Asn) n.3852G>A c.2929G>A (p.Asp977Asn) n.4709G>A n.4692G>A | dbSNP |
| 12 | g.45852684G>C | CA384491982 | ARID2 | c.4561G>C (p.Asp1521His) c.770G>C c.4482G>C c.4114G>C (p.Asp1372His) c.3391G>C (p.Asp1131His) c.385G>C (p.Asp129His) n.3852G>C c.2929G>C (p.Asp977His) n.4709G>C n.4692G>C | dbSNP gnomAD v4 |
| 12 | g.45852684G>T | CA384491983 | ARID2 | c.4561G>T (p.Asp1521Tyr) c.770G>T c.4482G>T c.4114G>T (p.Asp1372Tyr) c.3391G>T (p.Asp1131Tyr) c.385G>T (p.Asp129Tyr) n.3852G>T c.2929G>T (p.Asp977Tyr) n.4709G>T n.4692G>T | dbSNP |
| 12 | g.45852685A>C | CA384491984 | ARID2 | c.4562A>C (p.Asp1521Ala) c.771A>C c.4483A>C c.4115A>C (p.Asp1372Ala) c.3392A>C (p.Asp1131Ala) c.386A>C (p.Asp129Ala) n.3853A>C c.2930A>C (p.Asp977Ala) n.4710A>C n.4693A>C | |
| 12 | g.45852685A>G | CA384491985 | ARID2 | c.4562A>G (p.Asp1521Gly) c.771A>G c.4483A>G c.4115A>G (p.Asp1372Gly) c.3392A>G (p.Asp1131Gly) c.386A>G (p.Asp129Gly) n.3853A>G c.2930A>G (p.Asp977Gly) n.4710A>G n.4693A>G | gnomAD v4 COSMIC |
| 12 | g.45852685A>T | CA384491986 | ARID2 | c.4562A>T (p.Asp1521Val) c.771A>T c.4483A>T c.4115A>T (p.Asp1372Val) c.3392A>T (p.Asp1131Val) c.386A>T (p.Asp129Val) n.3853A>T c.2930A>T (p.Asp977Val) n.4710A>T n.4693A>T | dbSNP gnomAD v4 |
| 12 | g.45852686T>A | CA384491988 | ARID2 | c.4563T>A (p.Asp1521Glu) c.772T>A c.4484T>A c.4116T>A (p.Asp1372Glu) c.3393T>A (p.Asp1131Glu) c.387T>A (p.Asp129Glu) n.3854T>A c.2931T>A (p.Asp977Glu) n.4711T>A n.4694T>A | |
| 12 | g.45852686T>C | CA479694093 | ARID2 | c.4563T>C (p.Asp1521=) c.772T>C c.4484T>C c.4116T>C (p.Asp1372=) c.3393T>C (p.Asp1131=) c.387T>C (p.Asp129=) n.3854T>C c.2931T>C (p.Asp977=) n.4711T>C n.4694T>C | |
| 12 | g.45852686T>G | CA384491987 | ARID2 | c.4563T>G (p.Asp1521Glu) c.772T>G c.4484T>G c.4116T>G (p.Asp1372Glu) c.3393T>G (p.Asp1131Glu) c.387T>G (p.Asp129Glu) n.3854T>G c.2931T>G (p.Asp977Glu) n.4711T>G n.4694T>G | dbSNP |
| 12 | g.45852687A>C | CA384491989 | ARID2 | c.4564A>C (p.Thr1522Pro) c.773A>C c.4485A>C c.4117A>C (p.Thr1373Pro) c.3394A>C (p.Thr1132Pro) c.388A>C (p.Thr130Pro) n.3855A>C c.2932A>C (p.Thr978Pro) n.4712A>C n.4695A>C | |
| 12 | g.45852687A>G | CA384491990 | ARID2 | c.4564A>G (p.Thr1522Ala) c.773A>G c.4485A>G c.4117A>G (p.Thr1373Ala) c.3394A>G (p.Thr1132Ala) c.388A>G (p.Thr130Ala) n.3855A>G c.2932A>G (p.Thr978Ala) n.4712A>G n.4695A>G | dbSNP |
| 12 | g.45852687A>T | CA384491991 | ARID2 | c.4564A>T (p.Thr1522Ser) c.773A>T c.4485A>T c.4117A>T (p.Thr1373Ser) c.3394A>T (p.Thr1132Ser) c.388A>T (p.Thr130Ser) n.3855A>T c.2932A>T (p.Thr978Ser) n.4712A>T n.4695A>T | dbSNP |
| 12 | g.45852687dup | CA2618443336 | ARID2 | c.4564dup (p.Thr1522AsnfsTer2) c.773dup c.4485dup c.4117dup (p.Thr1373AsnfsTer2) c.3394dup (p.Thr1132AsnfsTer2) c.388dup (p.Thr130AsnfsTer2) n.3855dup c.2932dup (p.Thr978AsnfsTer2) n.4712dup n.4695dup | gnomAD v4 |
| 12 | g.45852688C>A | CA384491992 | ARID2 | c.4565C>A (p.Thr1522Asn) c.774C>A c.4486C>A c.4118C>A (p.Thr1373Asn) c.3395C>A (p.Thr1132Asn) c.389C>A (p.Thr130Asn) n.3856C>A c.2933C>A (p.Thr978Asn) n.4713C>A n.4696C>A | dbSNP |
| 12 | g.45852688C= | CA2033475732 | ARID2 | c.4565C= (p.Thr1522=) c.774C= c.4486C= c.4118C= (p.Thr1373=) c.3395C= (p.Thr1132=) c.389C= (p.Thr130=) n.3856C= c.2933C= (p.Thr978=) n.4713C= n.4696C= | |
| 12 | g.45852688C>G | CA6526688 | ARID2 | c.4565C>G (p.Thr1522Ser) c.774C>G c.4486C>G c.4118C>G (p.Thr1373Ser) c.3395C>G (p.Thr1132Ser) c.389C>G (p.Thr130Ser) n.3856C>G c.2933C>G (p.Thr978Ser) n.4713C>G n.4696C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.45852688C>T | CA384491993 | ARID2 | c.4565C>T (p.Thr1522Ile) c.774C>T c.4486C>T c.4118C>T (p.Thr1373Ile) c.3395C>T (p.Thr1132Ile) c.389C>T (p.Thr130Ile) n.3856C>T c.2933C>T (p.Thr978Ile) n.4713C>T n.4696C>T | dbSNP |
| 12 | g.45852689T>A | CA479694096 | ARID2 | c.4566T>A (p.Thr1522=) c.775T>A c.4487T>A c.4119T>A (p.Thr1373=) c.3396T>A (p.Thr1132=) c.390T>A (p.Thr130=) n.3857T>A c.2934T>A (p.Thr978=) n.4714T>A n.4697T>A | dbSNP |
| 12 | g.45852689T>C | CA479694095 | ARID2 | c.4566T>C (p.Thr1522=) c.775T>C c.4487T>C c.4119T>C (p.Thr1373=) c.3396T>C (p.Thr1132=) c.390T>C (p.Thr130=) n.3857T>C c.2934T>C (p.Thr978=) n.4714T>C n.4697T>C | dbSNP |
| 12 | g.45852689T>G | CA479694094 | ARID2 | c.4566T>G (p.Thr1522=) c.775T>G c.4487T>G c.4119T>G (p.Thr1373=) c.3396T>G (p.Thr1132=) c.390T>G (p.Thr130=) n.3857T>G c.2934T>G (p.Thr978=) n.4714T>G n.4697T>G | |
| 12 | g.45852690G>A | CA384491996 | ARID2 | c.4567G>A (p.Asp1523Asn) c.776G>A c.4488G>A c.4120G>A (p.Asp1374Asn) c.3397G>A (p.Asp1133Asn) c.391G>A (p.Asp131Asn) n.3858G>A c.2935G>A (p.Asp979Asn) n.4715G>A n.4698G>A | dbSNP |
| 12 | g.45852690G>C | CA384491995 | ARID2 | c.4567G>C (p.Asp1523His) c.776G>C c.4488G>C c.4120G>C (p.Asp1374His) c.3397G>C (p.Asp1133His) c.391G>C (p.Asp131His) n.3858G>C c.2935G>C (p.Asp979His) n.4715G>C n.4698G>C | dbSNP gnomAD v4 |
| 12 | g.45852690G>T | CA384491994 | ARID2 | c.4567G>T (p.Asp1523Tyr) c.776G>T c.4488G>T c.4120G>T (p.Asp1374Tyr) c.3397G>T (p.Asp1133Tyr) c.391G>T (p.Asp131Tyr) n.3858G>T c.2935G>T (p.Asp979Tyr) n.4715G>T n.4698G>T | |
| 12 | g.45852691A= | CA2033475733 | ARID2 | c.4568A= (p.Asp1523=) c.777A= c.4489A= c.4121A= (p.Asp1374=) c.3398A= (p.Asp1133=) c.392A= (p.Asp131=) n.3859A= c.2936A= (p.Asp979=) n.4716A= n.4699A= | |
| 12 | g.45852691A>C | CA384491997 | ARID2 | c.4568A>C (p.Asp1523Ala) c.777A>C c.4489A>C c.4121A>C (p.Asp1374Ala) c.3398A>C (p.Asp1133Ala) c.392A>C (p.Asp131Ala) n.3859A>C c.2936A>C (p.Asp979Ala) n.4716A>C n.4699A>C | |
| 12 | g.45852691A>G | CA384491998 | ARID2 | c.4568A>G (p.Asp1523Gly) c.777A>G c.4489A>G c.4121A>G (p.Asp1374Gly) c.3398A>G (p.Asp1133Gly) c.392A>G (p.Asp131Gly) n.3859A>G c.2936A>G (p.Asp979Gly) n.4716A>G n.4699A>G | ClinVar dbSNP |
| 12 | g.45852691A>T | CA384491999 | ARID2 | c.4568A>T (p.Asp1523Val) c.777A>T c.4489A>T c.4121A>T (p.Asp1374Val) c.3398A>T (p.Asp1133Val) c.392A>T (p.Asp131Val) n.3859A>T c.2936A>T (p.Asp979Val) n.4716A>T n.4699A>T | dbSNP |
| 12 | g.45852692T>A | CA384492000 | ARID2 | c.4569T>A (p.Asp1523Glu) c.778T>A c.4490T>A c.4122T>A (p.Asp1374Glu) c.3399T>A (p.Asp1133Glu) c.393T>A (p.Asp131Glu) n.3860T>A c.2937T>A (p.Asp979Glu) n.4717T>A n.4700T>A | dbSNP |
| 12 | g.45852692T>C | CA479694097 | ARID2 | c.4569T>C (p.Asp1523=) c.778T>C c.4490T>C c.4122T>C (p.Asp1374=) c.3399T>C (p.Asp1133=) c.393T>C (p.Asp131=) n.3860T>C c.2937T>C (p.Asp979=) n.4717T>C n.4700T>C | dbSNP gnomAD v4 |
| 12 | g.45852692T>G | CA384492001 | ARID2 | c.4569T>G (p.Asp1523Glu) c.778T>G c.4490T>G c.4122T>G (p.Asp1374Glu) c.3399T>G (p.Asp1133Glu) c.393T>G (p.Asp131Glu) n.3860T>G c.2937T>G (p.Asp979Glu) n.4717T>G n.4700T>G | dbSNP gnomAD v4 |
| 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 |