ClinVar Miner

List of variants in gene ARID1B reported as likely benign for not specified

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.2248-35G>A rs3734440 0.46405
NM_001374828.1(ARID1B):c.3235+38C>T rs9384530 0.08126
NM_001374828.1(ARID1B):c.1986+28T>C rs73572289 0.04166
NM_001374828.1(ARID1B):c.3235+21C>T rs9397998 0.01875
NM_001374828.1(ARID1B):c.4864A>T (p.Met1622Leu) rs34870395 0.01518
NM_001374828.1(ARID1B):c.1927A>G (p.Ile643Val) rs17318151 0.01456
NM_001374828.1(ARID1B):c.3106G>A (p.Gly1036Ser) rs34786733 0.00590
NM_001374828.1(ARID1B):c.1194A>C (p.Gly398=) rs112474841 0.00209
NM_001374828.1(ARID1B):c.3681C>T (p.Tyr1227=) rs61736269 0.00189
NM_001374828.1(ARID1B):c.2654C>T (p.Ser885Leu) rs150140314 0.00108
NM_001374828.1(ARID1B):c.963C>T (p.Ala321=) rs533517668 0.00107
NM_001374828.1(ARID1B):c.5384A>G (p.Asn1795Ser) rs140177120 0.00079
NM_001374828.1(ARID1B):c.1191C>A (p.Gly397=) rs184815562 0.00064
NM_001374828.1(ARID1B):c.4809C>T (p.Gly1603=) rs139903653 0.00027
NM_001374828.1(ARID1B):c.6318C>T (p.His2106=) rs142416998 0.00017
NM_001374828.1(ARID1B):c.6063C>T (p.Thr2021=) rs376113162 0.00015
NM_001374828.1(ARID1B):c.7011A>G (p.Glu2337=) rs756043689 0.00011
NM_001374828.1(ARID1B):c.1841T>C (p.Met614Thr) rs141260832 0.00008
NM_001374828.1(ARID1B):c.2142G>A (p.Met714Ile) rs142897795 0.00006
NM_001374828.1(ARID1B):c.2517C>T (p.Pro839=) rs541757080 0.00006
NM_001374828.1(ARID1B):c.5672C>T (p.Pro1891Leu) rs142466273 0.00006
NM_001374828.1(ARID1B):c.4714G>A (p.Gly1572Ser) rs141461351 0.00004
NM_001374828.1(ARID1B):c.4831C>T (p.Pro1611Ser) rs765827636 0.00004
NM_001374828.1(ARID1B):c.2102C>T (p.Pro701Leu) rs772078777 0.00003
NM_001374828.1(ARID1B):c.1962C>T (p.Ala654=) rs752755002 0.00002
NM_001374828.1(ARID1B):c.3235+7T>A rs367584953 0.00002
NM_001374828.1(ARID1B):c.5028G>A (p.Ala1676=) rs776881575 0.00002
NM_001374828.1(ARID1B):c.1987-10T>G rs1276255111 0.00001
NM_001374828.1(ARID1B):c.3588C>T (p.Val1196=) rs371828409 0.00001
NM_001374828.1(ARID1B):c.5027C>T (p.Ala1676Val) rs762698567 0.00001
NM_001374828.1(ARID1B):c.5240G>A (p.Arg1747Gln) rs762183842 0.00001
NM_001374828.1(ARID1B):c.6019C>T (p.Arg2007Trp) rs1377877762 0.00001
NM_001374828.1(ARID1B):c.6796G>A (p.Ala2266Thr) rs530084903 0.00001
NM_001374828.1(ARID1B):c.1170CGG[10] (p.Gly401_Gly402dup) rs587779747
NM_001374828.1(ARID1B):c.1170CGG[5] (p.Gly400_Gly402del) rs587779747
NM_001374828.1(ARID1B):c.1170CGG[6] (p.Gly401_Gly402del) rs587779747
NM_001374828.1(ARID1B):c.1170CGG[9] (p.Gly402dup) rs587779747
NM_001374828.1(ARID1B):c.1191_1196del (p.Gly401_Gly402del) rs1583025508
NM_001374828.1(ARID1B):c.1206_1223del (p.Ser403_Gly408del) rs755976776
NM_001374828.1(ARID1B):c.1211GAG[5] (p.Gly409_Gly411del) rs747790383
NM_001374828.1(ARID1B):c.1211GAG[6] (p.Gly410_Gly411del) rs747790383
NM_001374828.1(ARID1B):c.1211GAG[9] (p.Gly411dup) rs747790383
NM_001374828.1(ARID1B):c.1227AGGAGGAGCAGGAGC[1] (p.411GAGAG[1]) rs773423003
NM_001374828.1(ARID1B):c.1265_1270dup (p.Val422_Ala423dup) rs759630370
NM_001374828.1(ARID1B):c.1292CAG[4] (p.Ala433dup) rs797045267
NM_001374828.1(ARID1B):c.1303GGC[4] (p.Gly439_Gly440del) rs797045268
NM_001374828.1(ARID1B):c.1303GGC[5] (p.Gly440del) rs797045268
NM_001374828.1(ARID1B):c.1303GGC[7] (p.Gly440dup) rs797045268
NM_001374828.1(ARID1B):c.2016G>T (p.Val672=)
NM_001374828.1(ARID1B):c.3678C>T (p.Leu1226=) rs111368751
NM_001374828.1(ARID1B):c.4165A>G (p.Met1389Val) rs773883674
NM_001374828.1(ARID1B):c.4843G>A (p.Gly1615Ser) rs1274057762
NM_001374828.1(ARID1B):c.6793G>A (p.Asp2265Asn) rs2128398514
NM_001374828.1(ARID1B):c.6873G>A (p.Thr2291=) rs377350616
NM_001374828.1(ARID1B):c.954C>T (p.Gly318=) rs745740327

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