ClinVar Miner

List of variants in gene ARID1B reported as pathogenic by GeneDx

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Total variants: 69
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HGVS dbSNP
NM_020732.3(ARID1B):c.1044_1071del (p.Ala349fs) rs1554247989
NM_020732.3(ARID1B):c.1079dup (p.Ser361fs) rs1289468231
NM_020732.3(ARID1B):c.1202del (p.Gly401fs) rs1554248082
NM_020732.3(ARID1B):c.1245del (p.Thr416fs) rs886041707
NM_020732.3(ARID1B):c.1301_1341del (p.Gly434fs) rs1554248137
NM_020732.3(ARID1B):c.1360C>T (p.Gln454Ter) rs1057518213
NM_020732.3(ARID1B):c.1389_1398dup (p.Gln467fs) rs1131691339
NM_020732.3(ARID1B):c.1392_1402del (p.Gln467fs) rs1131691706
NM_020732.3(ARID1B):c.1392_1402dup (p.Gln468fs) rs1131691706
NM_020732.3(ARID1B):c.1400_1410del (p.Gln467fs) rs1085307818
NM_020732.3(ARID1B):c.1469_1488dup (p.Ser497fs) rs1554248228
NM_020732.3(ARID1B):c.1524_1525dup (p.Thr509fs) rs1554248273
NM_020732.3(ARID1B):c.2149C>T (p.Gln717Ter) rs753933273
NM_020732.3(ARID1B):c.2176_2177dup (p.His727fs) rs1554294665
NM_020732.3(ARID1B):c.2200_2201delinsT (p.Gly734fs) rs886041470
NM_020732.3(ARID1B):c.2201dup (p.Ser736fs) rs1554294674
NM_020732.3(ARID1B):c.2248C>T (p.Arg750Ter) rs797045272
NM_020732.3(ARID1B):c.2362C>T (p.Gln788Ter) rs1554298232
NM_020732.3(ARID1B):c.2393_2396del (p.Arg798fs) rs1085307695
NM_020732.3(ARID1B):c.2692C>T (p.Arg898Ter) rs794727977
NM_020732.3(ARID1B):c.2773C>T (p.Gln925Ter) rs1554226097
NM_020732.3(ARID1B):c.2776C>T (p.Gln926Ter) rs1057517704
NM_020732.3(ARID1B):c.2946del (p.Pro982_Met983insTer) rs1554228806
NM_020732.3(ARID1B):c.3016_3020dup (p.Ala1009fs) rs1057518387
NM_020732.3(ARID1B):c.3025+1G>A rs886039679
NM_020732.3(ARID1B):c.3051_3052insGA (p.Ser1018fs) rs1554229912
NM_020732.3(ARID1B):c.3223C>T (p.Arg1075Ter) rs387907144
NM_020732.3(ARID1B):c.3263C>G (p.Ser1088Ter) rs886039676
NM_020732.3(ARID1B):c.3304C>T (p.Arg1102Ter) rs387907141
NM_020732.3(ARID1B):c.3307_3308CT[1] (p.Tyr1104fs) rs1554231260
NM_020732.3(ARID1B):c.3361A>T (p.Lys1121Ter) rs886041623
NM_020732.3(ARID1B):c.3365G>A (p.Trp1122Ter) rs1554231803
NM_020732.3(ARID1B):c.3428del (p.Lys1143fs) rs1554231830
NM_020732.3(ARID1B):c.3520_3521del (p.Lys1174fs) rs886041493
NM_020732.3(ARID1B):c.3535C>T (p.Gln1179Ter) rs1554231904
NM_020732.3(ARID1B):c.3550+1G>A rs886039699
NM_020732.3(ARID1B):c.3596_3597del (p.Gly1199fs) rs1085307518
NM_020732.3(ARID1B):c.3843dup (p.Phe1282fs) rs1554233166
NM_020732.3(ARID1B):c.3862+1G>A rs1554233187
NM_020732.3(ARID1B):c.4009C>T (p.Arg1337Ter) rs773740590
NM_020732.3(ARID1B):c.4105C>T (p.Gln1369Ter) rs1554235028
NM_020732.3(ARID1B):c.4110+1G>C rs1554235041
NM_020732.3(ARID1B):c.4110G>A (p.Pro1370=) rs797045277
NM_020732.3(ARID1B):c.4152del (p.Lys1385fs) rs886041632
NM_020732.3(ARID1B):c.4273dup (p.Tyr1425fs) rs879253746
NM_020732.3(ARID1B):c.4322dup (p.His1441fs) rs886041463
NM_020732.3(ARID1B):c.4324G>T (p.Gly1442Ter) rs779375711
NM_020732.3(ARID1B):c.4365del (p.Ser1456fs) rs1554235699
NM_020732.3(ARID1B):c.4456C>T (p.Gln1486Ter) rs1064793482
NM_020732.3(ARID1B):c.4700_4701delinsAGT (p.Met1567fs) rs1554235934
NM_020732.3(ARID1B):c.4741C>T (p.Gln1581Ter) rs1554235950
NM_020732.3(ARID1B):c.4870C>T (p.Arg1624Ter) rs1554236040
NM_020732.3(ARID1B):c.4878_4890del (p.Thr1627fs) rs1554236045
NM_020732.3(ARID1B):c.4903del (p.Glu1635fs) rs1554236600
NM_020732.3(ARID1B):c.5338C>T (p.Gln1780Ter) rs750447037
NM_020732.3(ARID1B):c.5547dup (p.Ser1851fs) rs35441529
NM_020732.3(ARID1B):c.5566_5569AAGA[1] (p.Lys1857fs) rs886041706
NM_020732.3(ARID1B):c.5703dup (p.Lys1902Ter) rs886041878
NM_020732.3(ARID1B):c.5722C>T (p.Gln1908Ter) rs1554237606
NM_020732.3(ARID1B):c.5776C>T (p.Arg1926Ter) rs1554237658
NM_020732.3(ARID1B):c.5811G>A (p.Trp1937Ter) rs886041819
NM_020732.3(ARID1B):c.5965_5966del (p.Lys1989fs) rs1554237785
NM_020732.3(ARID1B):c.5968C>T (p.Arg1990Ter) rs797045283
NM_020732.3(ARID1B):c.6120_6130delinsGACTTG (p.Tyr2040_Ile2044delinsTer) rs886041665
NM_020732.3(ARID1B):c.6382C>T (p.Arg2128Ter) rs1554238072
NM_020732.3(ARID1B):c.6498_6508del (p.Val2167fs) rs1064793899
NM_020732.3(ARID1B):c.6629_6651del (p.Glu2210fs) rs886041804
NM_020732.3(ARID1B):c.760C>T (p.Gln254Ter) rs1554247662
NM_020732.3(ARID1B):c.769G>T (p.Gly257Ter) rs1057518256

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