ClinVar Miner

List of variants in gene ARID1B reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 115
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.1229G>C (p.Gly410Ala) rs1455234951 0.00019
NM_001374828.1(ARID1B):c.6344C>T (p.Pro2115Leu) rs368420323 0.00003
NM_001374828.1(ARID1B):c.2129C>T (p.Pro710Leu) rs558155146 0.00002
NM_001374828.1(ARID1B):c.3217A>G (p.Met1073Val) rs764460073 0.00002
NM_001374828.1(ARID1B):c.5096C>T (p.Pro1699Leu) rs1455506883 0.00002
NM_001374820.1(ARID1B):c.3473G>A (p.Arg1158Gln) rs940353111 0.00001
NM_001374828.1(ARID1B):c.1220G>C (p.Gly407Ala) rs1057522183 0.00001
NM_001374828.1(ARID1B):c.1544G>A (p.Ser515Asn) rs1297021537 0.00001
NM_001374828.1(ARID1B):c.1912C>G (p.Pro638Ala) rs1165021634 0.00001
NM_001374828.1(ARID1B):c.1934T>A (p.Ile645Asn) rs1057522610 0.00001
NM_001374828.1(ARID1B):c.2011G>A (p.Gly671Ser) rs1349709189 0.00001
NM_001374828.1(ARID1B):c.2906T>A (p.Met969Lys) rs1789981336 0.00001
NM_001374828.1(ARID1B):c.2909C>T (p.Pro970Leu) rs1057521656 0.00001
NM_001374828.1(ARID1B):c.3170C>G (p.Ser1057Cys) rs780818465 0.00001
NM_001374828.1(ARID1B):c.3236-1G>A rs752642190 0.00001
NM_001374828.1(ARID1B):c.4607G>A (p.Gly1536Asp) rs960896358 0.00001
NM_001374828.1(ARID1B):c.4772G>A (p.Arg1591His) rs780970034 0.00001
NM_001374828.1(ARID1B):c.6119A>G (p.Lys2040Arg) rs893554512 0.00001
NM_001374828.1(ARID1B):c.953G>A (p.Gly318Asp) rs1325822808 0.00001
NM_001374820.1(ARID1B):c.4756G>A (p.Asp1586Asn) rs1346882502
NM_001374828.1(ARID1B):c.*9A>C
NM_001374828.1(ARID1B):c.1025A>G (p.Gln342Arg) rs2114982895
NM_001374828.1(ARID1B):c.1222G>C (p.Gly408Arg) rs2114989675
NM_001374828.1(ARID1B):c.1257_1262dup (p.Ala421_Val422insGlyAla)
NM_001374828.1(ARID1B):c.1260A>C (p.Gly420=) rs2114991037
NM_001374828.1(ARID1B):c.1265T>C (p.Val422Ala)
NM_001374828.1(ARID1B):c.1301_1302delinsCAGGAGGC (p.Ala433_Gly434insAlaGly)
NM_001374828.1(ARID1B):c.1324G>A (p.Gly442Arg) rs2114993167
NM_001374828.1(ARID1B):c.1325G>A (p.Gly442Glu) rs2114993240
NM_001374828.1(ARID1B):c.1328G>C (p.Gly443Ala)
NM_001374828.1(ARID1B):c.1380C>T (p.Gly460=)
NM_001374828.1(ARID1B):c.1411G>A (p.Ala471Thr) rs1778968749
NM_001374828.1(ARID1B):c.1445C>A (p.Ala482Glu)
NM_001374828.1(ARID1B):c.1489G>A (p.Gly497Arg) rs2114997880
NM_001374828.1(ARID1B):c.1495A>G (p.Thr499Ala)
NM_001374828.1(ARID1B):c.1541G>A (p.Arg514Gln)
NM_001374828.1(ARID1B):c.1556G>C (p.Ser519Thr)
NM_001374828.1(ARID1B):c.1588C>T (p.Pro530Ser)
NM_001374828.1(ARID1B):c.1613C>G (p.Ser538Cys)
NM_001374828.1(ARID1B):c.1618G>C (p.Ala540Pro)
NM_001374828.1(ARID1B):c.1651C>A (p.Gln551Lys) rs1583027141
NM_001374828.1(ARID1B):c.1651C>G (p.Gln551Glu)
NM_001374828.1(ARID1B):c.1656_1657delinsCT (p.Ala553Ser)
NM_001374828.1(ARID1B):c.1826C>G (p.Pro609Arg)
NM_001374828.1(ARID1B):c.1851C>A (p.Asn617Lys)
NM_001374828.1(ARID1B):c.1989G>C (p.Met663Ile)
NM_001374828.1(ARID1B):c.2126_2127delinsGC (p.Gln709Arg)
NM_001374828.1(ARID1B):c.2224C>A (p.Gln742Lys)
NM_001374828.1(ARID1B):c.2380G>T (p.Ala794Ser)
NM_001374828.1(ARID1B):c.2523C>G (p.Ser841Arg) rs2128518014
NM_001374828.1(ARID1B):c.2545C>T (p.Pro849Ser)
NM_001374828.1(ARID1B):c.2582-2A>C rs1057524160
NM_001374828.1(ARID1B):c.2589G>A (p.Met863Ile)
NM_001374828.1(ARID1B):c.2734C>T (p.Pro912Ser) rs2128585878
NM_001374828.1(ARID1B):c.2807G>C (p.Ser936Thr) rs2128634027
NM_001374828.1(ARID1B):c.2900G>A (p.Gly967Glu) rs2128634373
NM_001374828.1(ARID1B):c.3079G>A (p.Ala1027Thr)
NM_001374828.1(ARID1B):c.3308A>G (p.Lys1103Arg)
NM_001374828.1(ARID1B):c.3329C>T (p.Pro1110Leu)
NM_001374828.1(ARID1B):c.3362_3363del (p.Gln1121fs) rs2128305623
NM_001374828.1(ARID1B):c.3446A>G (p.His1149Arg)
NM_001374828.1(ARID1B):c.3607A>C (p.Met1203Leu) rs760633180
NM_001374828.1(ARID1B):c.3703G>C (p.Gly1235Arg) rs2128317822
NM_001374828.1(ARID1B):c.3786C>G (p.Ser1262Arg) rs2128325168
NM_001374828.1(ARID1B):c.3860C>G (p.Pro1287Arg) rs754303482
NM_001374828.1(ARID1B):c.3887A>T (p.Lys1296Ile)
NM_001374828.1(ARID1B):c.3926C>T (p.Ser1309Leu) rs1321954955
NM_001374828.1(ARID1B):c.3953C>T (p.Pro1318Leu)
NM_001374828.1(ARID1B):c.4040C>T (p.Thr1347Ile) rs1793227770
NM_001374828.1(ARID1B):c.4051G>T (p.Gly1351Cys) rs2128339076
NM_001374828.1(ARID1B):c.4081G>A (p.Asp1361Asn)
NM_001374828.1(ARID1B):c.4117A>C (p.Lys1373Gln) rs1057522635
NM_001374828.1(ARID1B):c.4156G>A (p.Gly1386Ser)
NM_001374828.1(ARID1B):c.4232-9A>G
NM_001374828.1(ARID1B):c.4310C>G (p.Pro1437Arg)
NM_001374828.1(ARID1B):c.4382+3_4382+6del
NM_001374828.1(ARID1B):c.4501G>A (p.Gly1501Ser)
NM_001374828.1(ARID1B):c.4560C>A (p.Ser1520Arg) rs2128372595
NM_001374828.1(ARID1B):c.4573_4575del (p.Glu1525del) rs755476506
NM_001374828.1(ARID1B):c.4606G>C (p.Gly1536Arg)
NM_001374828.1(ARID1B):c.4651A>G (p.Ser1551Gly)
NM_001374828.1(ARID1B):c.4851C>A (p.Asn1617Lys) rs2128374397
NM_001374828.1(ARID1B):c.4853G>A (p.Arg1618His)
NM_001374828.1(ARID1B):c.5132C>T (p.Pro1711Leu) rs781086610
NM_001374828.1(ARID1B):c.5174T>C (p.Ile1725Thr)
NM_001374828.1(ARID1B):c.5194C>T (p.Pro1732Ser)
NM_001374828.1(ARID1B):c.5422G>A (p.Glu1808Lys) rs1554237014
NM_001374828.1(ARID1B):c.5592_5603del (p.Asp1864_Asp1867del) rs760357573
NM_001374828.1(ARID1B):c.5642A>G (p.Asp1881Gly)
NM_001374828.1(ARID1B):c.5695_5696delinsTT (p.Glu1899Leu)
NM_001374828.1(ARID1B):c.5816T>G (p.Leu1939Arg) rs2128393304
NM_001374828.1(ARID1B):c.6150C>G (p.Asp2050Glu) rs779936373
NM_001374828.1(ARID1B):c.6227G>A (p.Arg2076His) rs1351633854
NM_001374828.1(ARID1B):c.6278G>C (p.Gly2093Ala)
NM_001374828.1(ARID1B):c.6300G>T (p.Lys2100Asn)
NM_001374828.1(ARID1B):c.6323A>G (p.His2108Arg) rs2128396309
NM_001374828.1(ARID1B):c.6374A>G (p.Asp2125Gly)
NM_001374828.1(ARID1B):c.6387C>T (p.Ala2129=) rs1018664667
NM_001374828.1(ARID1B):c.6449C>T (p.Thr2150Met) rs2128397023
NM_001374828.1(ARID1B):c.6530A>G (p.His2177Arg) rs2128397478
NM_001374828.1(ARID1B):c.6545C>T (p.Pro2182Leu)
NM_001374828.1(ARID1B):c.6550G>T (p.Ala2184Ser)
NM_001374828.1(ARID1B):c.6560A>G (p.Gln2187Arg)
NM_001374828.1(ARID1B):c.6604C>G (p.Gln2202Glu)
NM_001374828.1(ARID1B):c.6650A>G (p.Asn2217Ser)
NM_001374828.1(ARID1B):c.6652A>C (p.Asn2218His)
NM_001374828.1(ARID1B):c.6677C>T (p.Pro2226Leu)
NM_001374828.1(ARID1B):c.6688C>T (p.Arg2230Cys)
NM_001374828.1(ARID1B):c.6785C>T (p.Ala2262Val)
NM_001374828.1(ARID1B):c.6835A>C (p.Ile2279Leu) rs2128398696
NM_001374828.1(ARID1B):c.6872C>T (p.Thr2291Met) rs1381434956
NM_001374828.1(ARID1B):c.6874A>G (p.Met2292Val)
NM_001374828.1(ARID1B):c.6888G>C (p.Gln2296His) rs1057522604
NM_001374828.1(ARID1B):c.7040A>G (p.Asp2347Gly)
NM_001374828.1(ARID1B):c.7051T>A (p.Ser2351Thr) rs2128399581

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