ClinVar Miner

List of variants in gene ARID1B reported as uncertain significance by Ambry Genetics

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Total variants: 32
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HGVS dbSNP
NM_020732.3(ARID1B):c.1029_1043del (p.Ala346_Ala350del) rs775733700
NM_020732.3(ARID1B):c.1082C>T (p.Ser361Leu)
NM_020732.3(ARID1B):c.1154G>A (p.Gly385Asp) rs1276959546
NM_020732.3(ARID1B):c.1190C>T (p.Ser397Leu) rs1235258455
NM_020732.3(ARID1B):c.1471G>A (p.Ala491Thr) rs1296293849
NM_020732.3(ARID1B):c.1837T>C (p.Tyr613His)
NM_020732.3(ARID1B):c.2195C>A (p.Pro732Gln) rs1318967699
NM_020732.3(ARID1B):c.2978A>T (p.Gln993Leu)
NM_020732.3(ARID1B):c.3238A>C (p.Met1080Leu)
NM_020732.3(ARID1B):c.3676A>T (p.Met1226Leu)
NM_020732.3(ARID1B):c.3785A>C (p.Gln1262Pro)
NM_020732.3(ARID1B):c.3946G>A (p.Gly1316Arg) rs199674889
NM_020732.3(ARID1B):c.4010G>A (p.Arg1337Gln)
NM_020732.3(ARID1B):c.4090G>A (p.Gly1364Ser) rs151115781
NM_020732.3(ARID1B):c.4240C>G (p.Pro1414Ala)
NM_020732.3(ARID1B):c.4241C>T (p.Pro1414Leu)
NM_020732.3(ARID1B):c.4658C>T (p.Ala1553Val) rs762698567
NM_020732.3(ARID1B):c.4673C>G (p.Ser1558Cys) rs1562346609
NM_020732.3(ARID1B):c.4780G>A (p.Gly1594Arg) rs1329932861
NM_020732.3(ARID1B):c.4813G>A (p.Glu1605Lys)
NM_020732.3(ARID1B):c.5099A>G (p.Glu1700Gly)
NM_020732.3(ARID1B):c.5127A>T (p.Lys1709Asn) rs1362951381
NM_020732.3(ARID1B):c.521C>T (p.Pro174Leu) rs1394730320
NM_020732.3(ARID1B):c.5357A>G (p.Lys1786Arg)
NM_020732.3(ARID1B):c.5741G>A (p.Arg1914Gln)
NM_020732.3(ARID1B):c.5755C>A (p.Leu1919Met) rs1562352930
NM_020732.3(ARID1B):c.5885A>G (p.Asp1962Gly)
NM_020732.3(ARID1B):c.6218A>C (p.Asn2073Thr) rs1430704414
NM_020732.3(ARID1B):c.6322C>T (p.Gln2108Ter) rs1554238035
NM_020732.3(ARID1B):c.652C>T (p.Pro218Ser)
NM_020732.3(ARID1B):c.76A>C (p.Lys26Gln) rs1475208851
NM_020732.3(ARID1B):c.980G>C (p.Gly327Ala) rs1455234951

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