ClinVar Miner

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

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Total variants: 44
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HGVS dbSNP
NM_020732.3(ARID1B):c.1029_1043del (p.Ala346_Ala350del) rs775733700
NM_020732.3(ARID1B):c.1043_1045CAG[4] (p.Ala350dup) rs797045267
NM_020732.3(ARID1B):c.1054_1056GGC[4] (p.Gly356_Gly357del) rs797045268
NM_020732.3(ARID1B):c.1054_1056GGC[5] (p.Gly357del) rs797045268
NM_020732.3(ARID1B):c.1054_1056GGC[7] (p.Gly357dup) rs797045268
NM_020732.3(ARID1B):c.1285A>G (p.Met429Val) rs199948752
NM_020732.3(ARID1B):c.1592T>C (p.Met531Thr) rs141260832
NM_020732.3(ARID1B):c.1678A>G (p.Ile560Val) rs17318151
NM_020732.3(ARID1B):c.1737+28T>C rs73572289
NM_020732.3(ARID1B):c.1932G>A (p.Met644Ile) rs142897795
NM_020732.3(ARID1B):c.2038-35G>A rs3734440
NM_020732.3(ARID1B):c.2307C>T (p.Pro769=) rs541757080
NM_020732.3(ARID1B):c.2444C>T (p.Ser815Leu) rs150140314
NM_020732.3(ARID1B):c.2896G>A (p.Gly966Ser) rs34786733
NM_020732.3(ARID1B):c.3025+21C>T rs9397998
NM_020732.3(ARID1B):c.3025+38C>T rs9384530
NM_020732.3(ARID1B):c.3219C>T (p.Val1073=) rs371828409
NM_020732.3(ARID1B):c.3309C>T (p.Leu1103=) rs111368751
NM_020732.3(ARID1B):c.3312C>T (p.Tyr1104=) rs61736269
NM_020732.3(ARID1B):c.3399C>T (p.Thr1133=) rs142391292
NM_020732.3(ARID1B):c.4345G>A (p.Gly1449Ser) rs141461351
NM_020732.3(ARID1B):c.4440C>T (p.Gly1480=) rs139903653
NM_020732.3(ARID1B):c.4495A>T (p.Met1499Leu) rs34870395
NM_020732.3(ARID1B):c.4658C>T (p.Ala1553Val) rs762698567
NM_020732.3(ARID1B):c.4871G>A (p.Arg1624Gln) rs762183842
NM_020732.3(ARID1B):c.5303C>T (p.Pro1768Leu) rs142466273
NM_020732.3(ARID1B):c.5694C>T (p.Thr1898=) rs376113162
NM_020732.3(ARID1B):c.640C>T (p.Pro214Ser) rs1301993972
NM_020732.3(ARID1B):c.6427G>A (p.Ala2143Thr) rs530084903
NM_020732.3(ARID1B):c.6504G>A (p.Thr2168=) rs377350616
NM_020732.3(ARID1B):c.6642A>G (p.Glu2214=) rs756043689
NM_020732.3(ARID1B):c.705C>T (p.Gly235=) rs745740327
NM_020732.3(ARID1B):c.714C>T (p.Ala238=) rs533517668
NM_020732.3(ARID1B):c.921_923CGG[10] (p.Gly318_Gly319dup) rs587779747
NM_020732.3(ARID1B):c.921_923CGG[5] (p.Gly317_Gly319del) rs587779747
NM_020732.3(ARID1B):c.921_923CGG[6] (p.Gly318_Gly319del) rs587779747
NM_020732.3(ARID1B):c.921_923CGG[9] (p.Gly319dup) rs587779747
NM_020732.3(ARID1B):c.942C>A (p.Gly314=) rs184815562
NM_020732.3(ARID1B):c.945A>C (p.Gly315=) rs112474841
NM_020732.3(ARID1B):c.957_974del (p.Ser320_Gly325del) rs755976776
NM_020732.3(ARID1B):c.962_964GAG[5] (p.Gly326_Gly328del) rs747790383
NM_020732.3(ARID1B):c.962_964GAG[6] (p.Gly327_Gly328del) rs747790383
NM_020732.3(ARID1B):c.962_964GAG[9] (p.Gly328dup) rs747790383
NM_020732.3(ARID1B):c.978_992AGGAGGAGCAGGAGC[1] (p.328_332GAGAG[1]) rs773423003

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