ClinVar Miner

List of variants in gene ARID1B studied for Inborn genetic diseases

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Total variants: 21
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HGVS dbSNP
NM_020732.3(ARID1B):c.1392_1402del (p.Gln467fs) rs1131691706
NM_020732.3(ARID1B):c.1618C>T (p.Gln540Ter) rs1554256703
NM_020732.3(ARID1B):c.1762G>T (p.Glu588Ter) rs201653711
NM_020732.3(ARID1B):c.2828dup (p.Glu944fs) rs1554226131
NM_020732.3(ARID1B):c.3183C>G (p.Tyr1061Ter) rs758570139
NM_020732.3(ARID1B):c.3223C>T (p.Arg1075Ter) rs387907144
NM_020732.3(ARID1B):c.3377del (p.Ala1126fs) rs1554231814
NM_020732.3(ARID1B):c.3993T>A (p.Tyr1331Ter) rs1554234424
NM_020732.3(ARID1B):c.4009C>T (p.Arg1337Ter) rs773740590
NM_020732.3(ARID1B):c.4171_4172del (p.Met1391fs) rs797044859
NM_020732.3(ARID1B):c.4470C>G (p.Tyr1490Ter) rs1554235792
NM_020732.3(ARID1B):c.4780G>A (p.Gly1594Arg) rs1329932861
NM_020732.3(ARID1B):c.4888dup (p.Asp1630fs) rs1554236054
NM_020732.3(ARID1B):c.5100del (p.Glu1700fs) rs1554237050
NM_020732.3(ARID1B):c.5404C>T (p.Arg1802Ter) rs797045282
NM_020732.3(ARID1B):c.5776C>T (p.Arg1926Ter) rs1554237658
NM_020732.3(ARID1B):c.6039G>A (p.Trp2013Ter) rs1554237848
NM_020732.3(ARID1B):c.6322C>T (p.Gln2108Ter) rs1554238035
NM_020732.3(ARID1B):c.6454C>T (p.Gln2152Ter) rs1554238093
NM_020732.3(ARID1B):c.6547C>T (p.Gln2183Ter) rs1308155037
NM_020732.3(ARID1B):c.717_730delinsG (p.Ala240fs) rs1554247637

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