ClinVar Miner

List of variants in gene ARID1B reported as uncertain significance for not specified

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Gene type:
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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.3105C>T (p.Pro1035=) rs144894118 0.00106
NM_001374828.1(ARID1B):c.2379T>C (p.His793=) rs370364530 0.00024
NM_001374828.1(ARID1B):c.2205A>T (p.Glu735Asp) rs139125255 0.00022
NM_001374828.1(ARID1B):c.5678C>T (p.Ala1893Val) rs201137071 0.00014
NM_001374828.1(ARID1B):c.6963G>A (p.Ala2321=) rs754242891 0.00009
NM_001374828.1(ARID1B):c.1628C>T (p.Ala543Val) rs797045270 0.00008
NM_001374828.1(ARID1B):c.4509C>T (p.Tyr1503=) rs377021700 0.00004
NM_001374828.1(ARID1B):c.5851G>A (p.Glu1951Lys) rs1451259945 0.00004
NM_001374828.1(ARID1B):c.1238G>C (p.Gly413Ala) rs749315126 0.00003
NM_001374828.1(ARID1B):c.2316A>G (p.Ala772=) rs745528262 0.00003
NM_001374828.1(ARID1B):c.3260T>C (p.Met1087Thr) rs371523255 0.00003
NM_001374828.1(ARID1B):c.5325G>T (p.Thr1775=) rs146620657 0.00003
NM_001374828.1(ARID1B):c.4314C>T (p.Ser1438=) rs371872657 0.00002
NM_001374828.1(ARID1B):c.6049C>T (p.Pro2017Ser) rs774509236 0.00002
NM_001374828.1(ARID1B):c.1410C>T (p.Ala470=) rs1401866270 0.00001
NM_001374828.1(ARID1B):c.3628G>A (p.Val1210Ile) rs758353662 0.00001
NM_001374828.1(ARID1B):c.4086A>G (p.Pro1362=) rs768227723 0.00001
NM_001374828.1(ARID1B):c.4611G>A (p.Pro1537=) rs749608995 0.00001
NM_001374828.1(ARID1B):c.5031C>T (p.Pro1677=) rs770164775 0.00001
NM_001374828.1(ARID1B):c.6258C>G (p.Ala2086=) rs781082506 0.00001
NM_001374828.1(ARID1B):c.6590C>T (p.Ser2197Leu) rs149978361 0.00001
NM_001374828.1(ARID1B):c.7031G>A (p.Arg2344Gln) rs1302430069 0.00001
NM_001374828.1(ARID1B):c.1136A>C (p.Asn379Thr) rs797045285
NM_001374828.1(ARID1B):c.1235CAGGAG[1] (p.412AG[1]) rs747438636
NM_001374828.1(ARID1B):c.1238GAGCAGGAG[1] (p.413GAG[1]) rs771557031
NM_001374828.1(ARID1B):c.1281_1295del (p.Ala429_Ala433del) rs1457993750
NM_001374828.1(ARID1B):c.1286C>T (p.Ala429Val)
NM_001374828.1(ARID1B):c.1303GGC[5] (p.Gly440del) rs797045268
NM_001374828.1(ARID1B):c.1492G>T (p.Ala498Ser)
NM_001374828.1(ARID1B):c.1620GGCGGCGGCGGG[1] (p.541AAAG[1]) rs1239601972
NM_001374828.1(ARID1B):c.1663G>A (p.Gly555Ser)
NM_001374828.1(ARID1B):c.2082A>C (p.Pro694=) rs756099753
NM_001374828.1(ARID1B):c.2211G>A (p.Leu737=) rs797045271
NM_001374828.1(ARID1B):c.2357C>T (p.Ala786Val)
NM_001374828.1(ARID1B):c.2440G>T (p.Val814Leu) rs765365713
NM_001374828.1(ARID1B):c.2907G>A (p.Met969Ile) rs1060499843
NM_001374828.1(ARID1B):c.3098G>A (p.Ser1033Asn) rs1554228777
NM_001374828.1(ARID1B):c.3195G>A (p.Pro1065=) rs537901478
NM_001374828.1(ARID1B):c.5172A>G (p.Pro1724=) rs1197819486
NM_001374828.1(ARID1B):c.5310T>C (p.Leu1770=) rs372621575
NM_001374828.1(ARID1B):c.6507G>C (p.Leu2169Phe)
NM_001374828.1(ARID1B):c.6626T>G (p.Leu2209Arg) rs1554237999
NM_001374828.1(ARID1B):c.988C>A (p.Arg330Ser) rs2114981971

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