ClinVar Miner

List of variants in gene ARID1B reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.2136+158T>C rs79498233 0.04269
NM_001374828.1(ARID1B):c.2762-168G>A rs35793467 0.02820
NM_001374828.1(ARID1B):c.3920-198T>A rs143278346 0.02779
NM_001374828.1(ARID1B):c.4382+126G>A rs146573721 0.02776
NM_001374828.1(ARID1B):c.3089+219G>A rs80114752 0.01297
NM_001374828.1(ARID1B):c.4479+19G>A rs142594004 0.01272
NM_001374828.1(ARID1B):c.2247+35347A>G rs115261623 0.01194
NM_001374828.1(ARID1B):c.3920-131T>A rs112902616 0.01160
NM_001374828.1(ARID1B):c.3920-157T>C rs111366896 0.01160
NM_001374828.1(ARID1B):c.4231+221C>T rs146157345 0.00988
NM_001374828.1(ARID1B):c.3828G>A (p.Glu1276=) rs61745451 0.00966
NM_001374828.1(ARID1B):c.4231+114G>A rs143021271 0.00896
NM_001374828.1(ARID1B):c.4231+257C>A rs140113760 0.00757
NM_001374828.1(ARID1B):c.2629C>T (p.Pro877Ser) rs114201726 0.00727
NM_001374828.1(ARID1B):c.2137-3T>A rs116661275 0.00673
NM_001374828.1(ARID1B):c.3106G>A (p.Gly1036Ser) rs34786733 0.00590
NM_001374828.1(ARID1B):c.2491+171C>T rs77899392 0.00575
NM_001374828.1(ARID1B):c.1987-29684T>A rs76268680 0.00548
NM_001374828.1(ARID1B):c.2247+35479A>G rs115341699 0.00481
NM_001374828.1(ARID1B):c.2137-314G>A rs115642857 0.00472
NM_001374828.1(ARID1B):c.5264-232C>T rs141743500 0.00431
NM_001374828.1(ARID1B):c.3345+12G>A rs111356146 0.00363
NM_001374828.1(ARID1B):c.2137-200G>A rs568652145 0.00357
NM_001374828.1(ARID1B):c.4479+223C>G rs147921840 0.00343
NM_001374828.1(ARID1B):c.4965C>T (p.Ile1655=) rs150010654 0.00340
NM_001374828.1(ARID1B):c.*200A>G rs188107152 0.00323
NM_001374828.1(ARID1B):c.4479+164G>A rs191237521 0.00187
NM_001374828.1(ARID1B):c.1771C>T (p.Pro591Ser) rs200682868 0.00062
NM_001374828.1(ARID1B):c.3715-12G>A rs374771644 0.00041
NM_001374828.1(ARID1B):c.4846A>G (p.Met1616Val) rs142788313 0.00026
NM_001374828.1(ARID1B):c.2205A>T (p.Glu735Asp) rs139125255 0.00022
NM_001374828.1(ARID1B):c.5679C>T (p.Ala1893=) rs146982427 0.00021
NM_001374828.1(ARID1B):c.3919+67A>T rs529570920 0.00020
NM_001374828.1(ARID1B):c.6318C>T (p.His2106=) rs142416998 0.00017
NM_001374828.1(ARID1B):c.1578C>T (p.Pro526=) rs760419444 0.00016
NM_001374828.1(ARID1B):c.4603T>G (p.Ser1535Ala) rs145516400 0.00016
NM_001374828.1(ARID1B):c.6063C>T (p.Thr2021=) rs376113162 0.00015
NM_001374828.1(ARID1B):c.5544A>C (p.Ala1848=) rs148922487 0.00014
NM_001374828.1(ARID1B):c.5678C>T (p.Ala1893Val) rs201137071 0.00014
NM_001374828.1(ARID1B):c.1452C>T (p.Gly484=) rs977827286 0.00012
NM_001374828.1(ARID1B):c.1801A>G (p.Met601Val) rs145785954 0.00010
NM_001374828.1(ARID1B):c.1337C>T (p.Ala446Val) rs748273011 0.00008
NM_001374828.1(ARID1B):c.1841T>C (p.Met614Thr) rs141260832 0.00008
NM_001374828.1(ARID1B):c.2731G>A (p.Gly911Ser) rs150249745 0.00007
NM_001374828.1(ARID1B):c.5464A>G (p.Met1822Val) rs369339813 0.00007
NM_001374828.1(ARID1B):c.6441G>A (p.Thr2147=) rs371980859 0.00007
NM_001374828.1(ARID1B):c.1379G>T (p.Gly460Val) rs1274183370 0.00006
NM_001374828.1(ARID1B):c.2517C>T (p.Pro839=) rs541757080 0.00006
NM_001374828.1(ARID1B):c.4440G>A (p.Pro1480=) rs374835455 0.00006
NM_001374828.1(ARID1B):c.4478C>T (p.Pro1493Leu) rs367809905 0.00006
NM_001374828.1(ARID1B):c.4896G>A (p.Glu1632=) rs773006123 0.00006
NM_001374828.1(ARID1B):c.5672C>T (p.Pro1891Leu) rs142466273 0.00006
NM_001374828.1(ARID1B):c.1296A>G (p.Ala432=) rs1339192099 0.00005
NM_001374828.1(ARID1B):c.5733A>G (p.Pro1911=) rs374294418 0.00005
NM_001374828.1(ARID1B):c.1712C>G (p.Pro571Arg) rs769085274 0.00004
NM_001374828.1(ARID1B):c.2761+31C>A rs185931486 0.00004
NM_001374828.1(ARID1B):c.5850C>T (p.Thr1950=) rs753997383 0.00004
NM_001374828.1(ARID1B):c.1238G>C (p.Gly413Ala) rs749315126 0.00003
NM_001374828.1(ARID1B):c.3260T>C (p.Met1087Thr) rs371523255 0.00003
NM_001374828.1(ARID1B):c.4701G>A (p.Pro1567=) rs373191607 0.00003
NM_001374828.1(ARID1B):c.2428G>A (p.Val810Ile) rs971544940 0.00002
NM_001374828.1(ARID1B):c.2615T>C (p.Met872Thr) rs761093701 0.00002
NM_001374828.1(ARID1B):c.1112A>G (p.Glu371Gly) rs980540915 0.00001
NM_001374828.1(ARID1B):c.1439C>T (p.Ser480Leu) rs1235258455 0.00001
NM_001374828.1(ARID1B):c.3867C>G (p.Val1289=) rs1024486739 0.00001
NM_001374828.1(ARID1B):c.4530C>T (p.His1510=) rs1009179822 0.00001
NM_001374828.1(ARID1B):c.4681A>G (p.Ile1561Val) rs780408339 0.00001
NM_001374828.1(ARID1B):c.*227_*228dup rs370046956
NM_001374828.1(ARID1B):c.*228del rs370046956
NM_001374828.1(ARID1B):c.1095C>G (p.Pro365=) rs971859263
NM_001374828.1(ARID1B):c.1170CGG[3] (p.Gly398_Gly402del) rs587779747
NM_001374828.1(ARID1B):c.1194AGG[3] (p.Gly402del) rs587779748
NM_001374828.1(ARID1B):c.1206_1229del (p.Ser403_Gly410del) rs1388229420
NM_001374828.1(ARID1B):c.1207_1209del (p.Ser403del) rs1469262535
NM_001374828.1(ARID1B):c.1211GAG[4] (p.Gly408_Gly411del) rs747790383
NM_001374828.1(ARID1B):c.1211GAG[5] (p.Gly409_Gly411del) rs747790383
NM_001374828.1(ARID1B):c.1227AGGAGGAGCAGGAGC[1] (p.411GAGAG[1]) rs773423003
NM_001374828.1(ARID1B):c.1235CAGGAG[1] (p.412AG[1]) rs747438636
NM_001374828.1(ARID1B):c.1235CAGGAG[3] (p.412AG[3]) rs747438636
NM_001374828.1(ARID1B):c.1235_1252dup (p.Ala412_Ala417dup) rs1167056329
NM_001374828.1(ARID1B):c.1265_1270dup (p.Val422_Ala423dup) rs759630370
NM_001374828.1(ARID1B):c.1278_1292del (p.Ala429_Ala433del) rs775733700
NM_001374828.1(ARID1B):c.1281GGC[5] (p.Ala433dup) rs764418312
NM_001374828.1(ARID1B):c.1303GGC[4] (p.Gly439_Gly440del) rs797045268
NM_001374828.1(ARID1B):c.1328G>A (p.Gly443Asp) rs1387431464
NM_001374828.1(ARID1B):c.1422C>G (p.Ser474Arg) rs1440588207
NM_001374828.1(ARID1B):c.1436G>C (p.Gly479Ala) rs760718156
NM_001374828.1(ARID1B):c.1620GGCGGCGGCGGG[1] (p.541AAAG[1]) rs1239601972
NM_001374828.1(ARID1B):c.1986+160del rs370597358
NM_001374828.1(ARID1B):c.2137-3dup rs541477699
NM_001374828.1(ARID1B):c.3195G>A (p.Pro1065=) rs537901478
NM_001374828.1(ARID1B):c.3346-128TA[8]
NM_001374828.1(ARID1B):c.3876C>G (p.Thr1292=) rs369218715
NM_001374828.1(ARID1B):c.3919+36G>C
NM_001374828.1(ARID1B):c.4059-10C>G rs189200947
NM_001374828.1(ARID1B):c.4220G>T (p.Gly1407Val) rs149389876
NM_001374828.1(ARID1B):c.4260G>C (p.Thr1420=) rs374823620
NM_001374828.1(ARID1B):c.4382+117C>G rs144114170
NM_001374828.1(ARID1B):c.5264-66G>T rs150647603
NM_001374828.1(ARID1B):c.5897G>A (p.Arg1966His)

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