ClinVar Miner

List of variants in gene MCCC1 reported as likely benign for not provided

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Gene type:
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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_020166.5(MCCC1):c.1595-181T>C rs112734059 0.02246
NM_020166.5(MCCC1):c.1268-90C>T rs140957052 0.01709
NM_020166.5(MCCC1):c.273+270C>T rs74380421 0.01143
NM_020166.5(MCCC1):c.2049+31G>A rs73068824 0.01038
NM_020166.5(MCCC1):c.1595-96C>T rs12330492 0.00882
NM_020166.5(MCCC1):c.1595-111A>G rs112025174 0.00864
NM_020166.5(MCCC1):c.1594+127G>T rs143318455 0.00814
NM_020166.5(MCCC1):c.873+36G>A rs114706421 0.00527
NM_020166.5(MCCC1):c.273+69A>G rs150193548 0.00505
NM_020166.5(MCCC1):c.1682-75G>T rs73068830 0.00487
NM_020166.5(MCCC1):c.726T>C (p.Asp242=) rs36206712 0.00445
NM_020166.5(MCCC1):c.2049+237T>C rs537365135 0.00418
NM_020166.5(MCCC1):c.*1A>T rs115605600 0.00230
NM_020166.5(MCCC1):c.294C>T (p.Ile98=) rs368288499 0.00009
NM_020166.5(MCCC1):c.1083+208C>G
NM_020166.5(MCCC1):c.1083+320del rs35283773
NM_020166.5(MCCC1):c.1268-89G>A rs73068841
NM_020166.5(MCCC1):c.156C>A (p.Val52=) rs398124353
NM_020166.5(MCCC1):c.1595-180A>G
NM_020166.5(MCCC1):c.1681+92_1681+100dup rs146243904
NM_020166.5(MCCC1):c.1851T>C (p.Thr617=) rs1577239619
NM_020166.5(MCCC1):c.192G>A (p.Val64=) rs1360164882
NM_020166.5(MCCC1):c.231G>A (p.Ala77=) rs144230304
NM_020166.5(MCCC1):c.492-92T>A rs112348183
NM_020166.5(MCCC1):c.54G>A (p.Arg18=) rs1577376491
NM_020166.5(MCCC1):c.874-6del rs755494348

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