ClinVar Miner

List of variants in gene ARID1B reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Total variants: 38
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HGVS dbSNP
NM_020732.3(ARID1B):c.-3A>G rs797045266
NM_020732.3(ARID1B):c.103_105TCC[6] (p.Ser41del) rs770512547
NM_020732.3(ARID1B):c.1375G>A (p.Ala459Thr) rs587779740
NM_020732.3(ARID1B):c.1379C>T (p.Ala460Val) rs797045270
NM_020732.3(ARID1B):c.1872A>C (p.Pro624=) rs756099753
NM_020732.3(ARID1B):c.197A>G (p.Asn66Ser) rs776745618
NM_020732.3(ARID1B):c.1995A>T (p.Glu665Asp) rs139125255
NM_020732.3(ARID1B):c.2001G>A (p.Leu667=) rs797045271
NM_020732.3(ARID1B):c.2106A>G (p.Ala702=) rs745528262
NM_020732.3(ARID1B):c.2169T>C (p.His723=) rs370364530
NM_020732.3(ARID1B):c.2799G>A (p.Pro933=) rs587779742
NM_020732.3(ARID1B):c.2888G>A (p.Ser963Asn) rs1554228777
NM_020732.3(ARID1B):c.288_311del (p.His98_Ala105del) rs1554247278
NM_020732.3(ARID1B):c.2895C>T (p.Pro965=) rs144894118
NM_020732.3(ARID1B):c.2985G>A (p.Pro995=) rs537901478
NM_020732.3(ARID1B):c.3050T>C (p.Met1017Thr) rs371523255
NM_020732.3(ARID1B):c.3259G>A (p.Val1087Ile) rs758353662
NM_020732.3(ARID1B):c.3796A>G (p.Met1266Val) rs773883674
NM_020732.3(ARID1B):c.3945C>T (p.Ser1315=) rs371872657
NM_020732.3(ARID1B):c.4140C>T (p.Tyr1380=) rs377021700
NM_020732.3(ARID1B):c.4474G>A (p.Gly1492Ser) rs1274057762
NM_020732.3(ARID1B):c.4941T>C (p.Leu1647=) rs372621575
NM_020732.3(ARID1B):c.4956G>T (p.Thr1652=) rs146620657
NM_020732.3(ARID1B):c.5015A>G (p.Asn1672Ser) rs140177120
NM_020732.3(ARID1B):c.5309C>T (p.Ala1770Val) rs201137071
NM_020732.3(ARID1B):c.5650C>T (p.Arg1884Trp) rs1377877762
NM_020732.3(ARID1B):c.5680C>T (p.Pro1894Ser) rs774509236
NM_020732.3(ARID1B):c.5802C>T (p.Ile1934=) rs142499766
NM_020732.3(ARID1B):c.5889C>G (p.Ala1963=) rs781082506
NM_020732.3(ARID1B):c.6257T>G (p.Leu2086Arg) rs1554237999
NM_020732.3(ARID1B):c.637C>T (p.Pro213Ser) rs797045284
NM_020732.3(ARID1B):c.6594G>A (p.Ala2198=) rs754242891
NM_020732.3(ARID1B):c.6662G>A (p.Arg2221Gln) rs1302430069
NM_020732.3(ARID1B):c.678C>T (p.Ala226=) rs1450163641
NM_020732.3(ARID1B):c.887A>C (p.Asn296Thr) rs797045285
NM_020732.3(ARID1B):c.986_991CAGGAG[1] (p.329_330AG[1]) rs747438636
NM_020732.3(ARID1B):c.989G>C (p.Gly330Ala) rs749315126
NM_020732.3(ARID1B):c.989_997GAGCAGGAG[1] (p.330_332GAG[1]) rs771557031

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