ClinVar Miner

List of variants in gene DNMT1 reported as likely benign for not provided

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Gene type:
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Total variants: 63
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HGVS dbSNP
NC_000019.10:g.10146214_10146215del rs553864921
NM_001130823.3(DNMT1):c.1044-3del rs780538171
NM_001130823.3(DNMT1):c.1171-7C>T rs1168540279
NM_001130823.3(DNMT1):c.1280+9A>T rs769934389
NM_001130823.3(DNMT1):c.1281-8C>T rs1256774103
NM_001130823.3(DNMT1):c.1296C>T (p.His432=) rs780223552
NM_001130823.3(DNMT1):c.1314C>T (p.Ile438=) rs201487376
NM_001130823.3(DNMT1):c.1458T>C (p.Asp486=) rs369649047
NM_001130823.3(DNMT1):c.1493-11_1493-9dup rs1599366595
NM_001130823.3(DNMT1):c.1749C>T (p.Ala583=) rs569985466
NM_001130823.3(DNMT1):c.1777C>T (p.Leu593=) rs765260449
NM_001130823.3(DNMT1):c.1812T>C (p.Ala604=) rs770886671
NM_001130823.3(DNMT1):c.1911C>T (p.Thr637=) rs745677290
NM_001130823.3(DNMT1):c.204A>G (p.Leu68=) rs1477285670
NM_001130823.3(DNMT1):c.2117+9G>A rs1394137491
NM_001130823.3(DNMT1):c.2268T>C (p.Thr756=) rs374841430
NM_001130823.3(DNMT1):c.2385C>T (p.Val795=) rs1420828727
NM_001130823.3(DNMT1):c.2430C>T (p.Ala810=) rs1316143407
NM_001130823.3(DNMT1):c.2451A>G (p.Thr817=) rs112405538
NM_001130823.3(DNMT1):c.2478C>T (p.Asp826=) rs974103564
NM_001130823.3(DNMT1):c.2649G>C (p.Leu883=) rs764724670
NM_001130823.3(DNMT1):c.2693C>T (p.Thr898Ile) rs201213597
NM_001130823.3(DNMT1):c.2700A>G (p.Pro900=) rs1599358442
NM_001130823.3(DNMT1):c.2706G>A (p.Glu902=) rs777958103
NM_001130823.3(DNMT1):c.2720+8C>T rs1043815439
NM_001130823.3(DNMT1):c.3021C>T (p.Tyr1007=) rs1599352087
NM_001130823.3(DNMT1):c.3069C>G (p.Gly1023=) rs1599351980
NM_001130823.3(DNMT1):c.3099G>A (p.Arg1033=) rs1257621088
NM_001130823.3(DNMT1):c.3117-8G>A rs769623856
NM_001130823.3(DNMT1):c.3141T>C (p.Thr1047=) rs1377826866
NM_001130823.3(DNMT1):c.3459C>T (p.Pro1153=) rs1599347635
NM_001130823.3(DNMT1):c.3546C>T (p.Ala1182=) rs775884429
NM_001130823.3(DNMT1):c.3594C>T (p.Pro1198=) rs375481300
NM_001130823.3(DNMT1):c.3647C>G (p.Ala1216Gly) rs1223800609
NM_001130823.3(DNMT1):c.3807-10C>T rs1298476442
NM_001130823.3(DNMT1):c.3807-4A>G rs1599345906
NM_001130823.3(DNMT1):c.3936C>T (p.Phe1312=) rs367637414
NM_001130823.3(DNMT1):c.3949-9dup rs780030001
NM_001130823.3(DNMT1):c.3999C>T (p.Ala1333=) rs747144567
NM_001130823.3(DNMT1):c.4032G>C (p.Pro1344=) rs150774582
NM_001130823.3(DNMT1):c.4170G>A (p.Leu1390=) rs758009053
NM_001130823.3(DNMT1):c.4209C>T (p.Ser1403=) rs1599342899
NM_001130823.3(DNMT1):c.4392C>T (p.Asp1464=) rs200416276
NM_001130823.3(DNMT1):c.4491C>T (p.Ala1497=) rs776248336
NM_001130823.3(DNMT1):c.4539C>T (p.Pro1513=) rs756678908
NM_001130823.3(DNMT1):c.4590T>C (p.Tyr1530=) rs1599339925
NM_001130823.3(DNMT1):c.4626C>T (p.Thr1542=) rs760037814
NM_001130823.3(DNMT1):c.4635C>T (p.Asn1545=) rs1599339829
NM_001130823.3(DNMT1):c.4657-7C>T rs1336734666
NM_001130823.3(DNMT1):c.4659C>T (p.Gly1553=) rs1599339344
NM_001130823.3(DNMT1):c.4671C>T (p.His1557=) rs779173731
NM_001130823.3(DNMT1):c.4722C>A (p.Gly1574=) rs369472235
NM_001130823.3(DNMT1):c.4752C>T (p.Asn1584=) rs1599339143
NM_001130823.3(DNMT1):c.4816T>C (p.Leu1606=) rs147713850
NM_001130823.3(DNMT1):c.4839G>A (p.Leu1613=) rs1599336526
NM_001130823.3(DNMT1):c.493+1G>A rs975957081
NM_001130823.3(DNMT1):c.494-10_494-8del rs749027264
NM_001130823.3(DNMT1):c.569+126C>T rs186792836
NM_001130823.3(DNMT1):c.694C>A (p.Pro232Thr) rs374856119
NM_001130823.3(DNMT1):c.804-57C>T rs188576364
NM_001130823.3(DNMT1):c.891+9G>A rs375464404
NM_001130823.3(DNMT1):c.957A>G (p.Glu319=) rs1179101598
NM_001130823.3(DNMT1):c.984T>A (p.Ser328=) rs778332634

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