ClinVar Miner

List of variants in gene DNMT1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NC_000019.10:g.10146214_10146215del
NM_001130823.3(DNMT1):c.-45C>T rs375666082
NM_001130823.3(DNMT1):c.1053A>G (p.Lys351=) rs139355567
NM_001130823.3(DNMT1):c.1116C>T (p.Cys372=) rs147382114
NM_001130823.3(DNMT1):c.1131C>T (p.Asp377=) rs760064256
NM_001130823.3(DNMT1):c.1206G>C (p.Leu402=) rs147235870
NM_001130823.3(DNMT1):c.1245T>C (p.Tyr415=) rs574479254
NM_001130823.3(DNMT1):c.1280+14C>G rs372425803
NM_001130823.3(DNMT1):c.1536G>A (p.Ala512=) rs764039807
NM_001130823.3(DNMT1):c.1707C>T (p.His569=) rs777372271
NM_001130823.3(DNMT1):c.1722G>A (p.Val574=) rs140376680
NM_001130823.3(DNMT1):c.1832+10C>T rs371792523
NM_001130823.3(DNMT1):c.1896G>A (p.Thr632=) rs202058239
NM_001130823.3(DNMT1):c.2010C>T (p.Gly670=) rs374476495
NM_001130823.3(DNMT1):c.2020-10C>T rs369373339
NM_001130823.3(DNMT1):c.2382-15G>A rs111694626
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792
NM_001130823.3(DNMT1):c.2587-18G>A rs761123463
NM_001130823.3(DNMT1):c.2587-19C>T rs199713998
NM_001130823.3(DNMT1):c.2626G>A (p.Gly876Arg) rs62621087
NM_001130823.3(DNMT1):c.2676C>T (p.Phe892=) rs139861062
NM_001130823.3(DNMT1):c.2720+8C>T rs1043815439
NM_001130823.3(DNMT1):c.2835C>T (p.Asn945=) rs539948794
NM_001130823.3(DNMT1):c.2894+15G>A rs370596200
NM_001130823.3(DNMT1):c.2913C>T (p.Pro971=) rs780156725
NM_001130823.3(DNMT1):c.3117-9C>T rs199546819
NM_001130823.3(DNMT1):c.3186C>T (p.Asp1062=) rs138736029
NM_001130823.3(DNMT1):c.3310-18C>T rs199617900
NM_001130823.3(DNMT1):c.3408C>G (p.Pro1136=) rs144675407
NM_001130823.3(DNMT1):c.3524-16G>A rs199694630
NM_001130823.3(DNMT1):c.3807-14C>T rs371376513
NM_001130823.3(DNMT1):c.3963C>T (p.Gly1321=) rs375300708
NM_001130823.3(DNMT1):c.4032G>A (p.Pro1344=) rs150774582
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys) rs138841970
NM_001130823.3(DNMT1):c.4115+16C>T rs775701177
NM_001130823.3(DNMT1):c.4116-9C>T rs1057520947
NM_001130823.3(DNMT1):c.4293+17A>G rs1416290728
NM_001130823.3(DNMT1):c.4368C>T (p.Pro1456=) rs2229858
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.3(DNMT1):c.4490-4C>T rs764747230
NM_001130823.3(DNMT1):c.4503C>T (p.Cys1501=) rs149271718
NM_001130823.3(DNMT1):c.4599C>T (p.Leu1533=) rs145860233
NM_001130823.3(DNMT1):c.45C>A (p.Val15=) rs748347654
NM_001130823.3(DNMT1):c.4626C>T (p.Thr1542=)
NM_001130823.3(DNMT1):c.4734C>T (p.Thr1578=) rs1057523396
NM_001130823.3(DNMT1):c.4773+18C>T rs183300496
NM_001130823.3(DNMT1):c.483T>C (p.Thr161=) rs764496230
NM_001130823.3(DNMT1):c.493+8C>T rs138998574
NM_001130823.3(DNMT1):c.569+126C>T
NM_001130823.3(DNMT1):c.683+16A>C rs370399482
NM_001130823.3(DNMT1):c.80+11T>C rs368945230
NM_001130823.3(DNMT1):c.803+11C>T rs377632120
NM_001130823.3(DNMT1):c.804-57C>T
NM_001130823.3(DNMT1):c.890A>G (p.Lys297Arg) rs201025441
NM_001130823.3(DNMT1):c.925C>G (p.Leu309Val) rs61758430
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044

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