ClinVar Miner

List of variants in gene ARID1B reported as likely benign for History of neurodevelopmental disorder

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Total variants: 62
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HGVS dbSNP
NM_017519.2(ARID1B):c.1016_1021dup (p.Val339_Ala340dup) rs759630370
NM_017519.2(ARID1B):c.1017_1019GGC[6] (p.Ala349_Ala350dup) rs765410747
NM_017519.2(ARID1B):c.1029_1040del (p.Ala347_Ala350del) rs763063242
NM_017519.2(ARID1B):c.1032_1034GGC[5] (p.Ala350dup) rs764418312
NM_017519.2(ARID1B):c.1041_1046dup (p.Ala349_Ala350dup) rs1562377904
NM_017519.2(ARID1B):c.1043_1045CAG[4] (p.Ala350dup) rs797045267
NM_017519.2(ARID1B):c.1043_1045CAG[5] (p.Ala349_Ala350dup) rs797045267
NM_017519.2(ARID1B):c.1054_1056GGC[5] (p.Gly357del) rs797045268
NM_017519.2(ARID1B):c.1370_1372CGG[3] (p.Ala460del) rs757953295
NM_017519.2(ARID1B):c.1385_1387CGG[4] (p.Ala464dup) rs1367431735
NM_017519.2(ARID1B):c.679_680delinsCC (p.Val227Pro) rs1554247605
NM_017519.2(ARID1B):c.921_923CGG[10] (p.Gly318_Gly319dup) rs587779747
NM_017519.2(ARID1B):c.921_923CGG[5] (p.Gly317_Gly319del) rs587779747
NM_017519.2(ARID1B):c.921_923CGG[6] (p.Gly318_Gly319del) rs587779747
NM_017519.2(ARID1B):c.945_947AGG[5] (p.Gly319dup) rs587779748
NM_017519.2(ARID1B):c.962_964GAG[10] (p.Gly327_Gly328dup) rs747790383
NM_017519.2(ARID1B):c.962_964GAG[11] (p.Gly326_Gly328dup) rs747790383
NM_017519.2(ARID1B):c.962_964GAG[9] (p.Gly328dup) rs747790383
NM_017519.2(ARID1B):c.986_991CAGGAG[3] (p.329_330AG[3]) rs747438636
NM_017519.2(ARID1B):c.996_1001AGGAGC[3] (p.333_334GA[4]) rs1323804393
NM_020732.3(ARID1B):c.1088C>T (p.Ala363Val) rs748273011
NM_020732.3(ARID1B):c.1102C>T (p.Leu368=) rs1562378059
NM_020732.3(ARID1B):c.1329C>T (p.Pro443=) rs760419444
NM_020732.3(ARID1B):c.1632G>A (p.Pro544=) rs142939952
NM_020732.3(ARID1B):c.1714G>A (p.Gly572Arg) rs151093357
NM_020732.3(ARID1B):c.1920G>A (p.Pro640=) rs374876774
NM_020732.3(ARID1B):c.1977C>T (p.Pro659=) rs146240413
NM_020732.3(ARID1B):c.2070G>A (p.Thr690=) rs201290874
NM_020732.3(ARID1B):c.2444C>T (p.Ser815Leu) rs150140314
NM_020732.3(ARID1B):c.2862G>C (p.Ala954=) rs148749268
NM_020732.3(ARID1B):c.2895C>T (p.Pro965=) rs144894118
NM_020732.3(ARID1B):c.2976G>T (p.Thr992=) rs755525381
NM_020732.3(ARID1B):c.3120C>T (p.Pro1040=) rs752231248
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.3628C>G (p.Leu1210Val) rs138482029
NM_020732.3(ARID1B):c.3771C>T (p.Asn1257=) rs370523060
NM_020732.3(ARID1B):c.3891G>C (p.Thr1297=) rs374823620
NM_020732.3(ARID1B):c.4071G>A (p.Pro1357=) rs374835455
NM_020732.3(ARID1B):c.4294A>G (p.Met1432Val) rs745566888
NM_020732.3(ARID1B):c.4305G>A (p.Pro1435=) rs566865279
NM_020732.3(ARID1B):c.4659G>A (p.Ala1553=) rs776881575
NM_020732.3(ARID1B):c.4671G>A (p.Ala1557=) rs374125873
NM_020732.3(ARID1B):c.5015A>G (p.Asn1672Ser) rs140177120
NM_020732.3(ARID1B):c.5099A>G (p.Glu1700Gly) rs149841055
NM_020732.3(ARID1B):c.5289C>T (p.Ile1763=) rs533990759
NM_020732.3(ARID1B):c.5307C>T (p.Asp1769=) rs537400492
NM_020732.3(ARID1B):c.5310C>T (p.Ala1770=) rs146982427
NM_020732.3(ARID1B):c.5546C>G (p.Pro1849Arg) rs202194222
NM_020732.3(ARID1B):c.5607A>G (p.Gln1869=) rs1303216691
NM_020732.3(ARID1B):c.5694C>T (p.Thr1898=) rs376113162
NM_020732.3(ARID1B):c.5802C>T (p.Ile1934=) rs142499766
NM_020732.3(ARID1B):c.6072G>A (p.Thr2024=) rs371980859
NM_020732.3(ARID1B):c.6090C>T (p.Asn2030=) rs939615492
NM_020732.3(ARID1B):c.6294G>C (p.Leu2098=) rs1562354325
NM_020732.3(ARID1B):c.6342A>G (p.Thr2114=) rs147679171
NM_020732.3(ARID1B):c.6594G>A (p.Ala2198=) rs754242891
NM_020732.3(ARID1B):c.6654C>T (p.His2218=) rs183572405
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.941_942insAGG (p.Gly319dup) rs1562377373
NM_020732.3(ARID1B):c.945A>C (p.Gly315=) rs112474841

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