ClinVar Miner

List of variants in gene DNMT1 reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001130823.3(DNMT1):c.1782A>G (p.Thr594=) rs721186 0.99062
NM_001130823.3(DNMT1):c.1389A>G (p.Pro463=) rs2228611 0.50821
NM_001130823.3(DNMT1):c.1832+14A>G rs2114724 0.50605
NM_001130823.3(DNMT1):c.979A>G (p.Ile327Val) rs2228612 0.10575
NM_001130823.3(DNMT1):c.1632C>A (p.Ile544=) rs2228613 0.06881
NM_001130823.3(DNMT1):c.206G>A (p.Arg69His) rs61750053 0.01134
NM_001130823.3(DNMT1):c.3939C>T (p.Gly1313=) rs142903301 0.00977
NM_001130823.3(DNMT1):c.290A>G (p.His97Arg) rs16999593 0.00959
NM_001130823.3(DNMT1):c.1095C>T (p.His365=) rs116502459 0.00699
NM_001130823.3(DNMT1):c.1500C>T (p.Ala500=) rs75443147 0.00552
NM_001130823.3(DNMT1):c.4294-17C>A rs79585069 0.00551
NM_001130823.3(DNMT1):c.4294-19G>C rs2290683 0.00551
NM_001130823.3(DNMT1):c.2382-4C>T rs74505694 0.00548
NM_001130823.3(DNMT1):c.2463C>T (p.Leu821=) rs61750051 0.00377
NM_001130823.3(DNMT1):c.891+8C>T rs117294281 0.00299
NM_001130823.3(DNMT1):c.925C>G (p.Leu309Val) rs61758430 0.00295
NM_001130823.3(DNMT1):c.1944C>T (p.Phe648=) rs61750052 0.00249
NM_001130823.3(DNMT1):c.996C>T (p.Asp332=) rs16999358 0.00243
NM_001130823.3(DNMT1):c.358G>C (p.Val120Leu) rs75616428 0.00240
NM_001130823.3(DNMT1):c.150C>T (p.His50=) rs146112081 0.00182
NM_001130823.3(DNMT1):c.1206G>C (p.Leu402=) rs147235870 0.00163
NM_001130823.3(DNMT1):c.2117+13G>A rs112660071 0.00153
NM_001130823.3(DNMT1):c.768+12T>A rs189898346 0.00123
NM_001130823.3(DNMT1):c.768+18C>A rs200380915 0.00123
NM_001130823.3(DNMT1):c.683+16A>C rs370399482 0.00119
NM_001130823.3(DNMT1):c.2676C>T (p.Phe892=) rs139861062 0.00108
NM_001130823.3(DNMT1):c.4368C>T (p.Pro1456=) rs2229858 0.00101
NM_001130823.3(DNMT1):c.2382-15G>A rs111694626 0.00071
NM_001130823.3(DNMT1):c.3492C>T (p.Cys1164=) rs140951214 0.00053
NM_001130823.3(DNMT1):c.1224C>T (p.Asn408=) rs199584370 0.00035
NM_001130823.3(DNMT1):c.3408C>G (p.Pro1136=) rs144675407 0.00035
NM_001130823.3(DNMT1):c.803+11C>T rs377632120 0.00034
NM_001130823.3(DNMT1):c.1280+14C>G rs372425803 0.00032
NM_001130823.3(DNMT1):c.2010C>T (p.Gly670=) rs374476495 0.00027
NM_001130823.3(DNMT1):c.4077G>C (p.Val1359=) rs577069147 0.00019
NM_001130823.3(DNMT1):c.633A>G (p.Glu211=) rs141264613 0.00017
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044 0.00011
NM_001130823.3(DNMT1):c.4878G>A (p.Glu1626=) rs776749454 0.00010
NM_001130823.3(DNMT1):c.4032G>A (p.Pro1344=) rs150774582 0.00009
NM_001130823.3(DNMT1):c.1722G>A (p.Val574=) rs140376680 0.00006
NM_001130823.3(DNMT1):c.1845G>A (p.Ala615=) rs761852984 0.00006
NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys) rs201308454 0.00006
NM_001130823.3(DNMT1):c.1932C>T (p.Phe644=) rs370444117 0.00005
NM_001130823.3(DNMT1):c.2019+19G>A rs531721071 0.00005
NM_001130823.3(DNMT1):c.3351C>T (p.Asn1117=) rs534263445 0.00005
NM_001130823.3(DNMT1):c.3714C>T (p.Gly1238=) rs761502229 0.00001
NM_001130823.3(DNMT1):c.4860C>T (p.Ala1620=) rs576877219 0.00001
NM_001130823.3(DNMT1):c.1044-8del rs59599980
NM_001130823.3(DNMT1):c.1044-9_1044-8del rs59599980
NM_001130823.3(DNMT1):c.1905C>G (p.Thr635=)
NM_001130823.3(DNMT1):c.2381+18del
NM_001130823.3(DNMT1):c.2382-16C>G rs199909957
NM_001130823.3(DNMT1):c.2697G>A (p.Gln899=) rs530293931
NM_001130823.3(DNMT1):c.2720+13del
NM_001130823.3(DNMT1):c.429C>T (p.Ser143=)
NM_001130823.3(DNMT1):c.432T>C (p.Asp144=)
NM_001130823.3(DNMT1):c.497A>G (p.Glu166Gly)
NM_001130823.3(DNMT1):c.769-14dup

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