ClinVar Miner

List of variants in gene DNMT1 studied for Dementia, Deafness, and Sensory Neuropathy

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Total variants: 70
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HGVS dbSNP
NM_001130823.2(DNMT1):c.*323C>G rs146694575
NM_001130823.2(DNMT1):c.-72C>T rs779334757
NM_001130823.3(DNMT1):c.*126A>G rs886054126
NM_001130823.3(DNMT1):c.*165T>G rs192952800
NM_001130823.3(DNMT1):c.*18C>A rs778467461
NM_001130823.3(DNMT1):c.*18C>T rs778467461
NM_001130823.3(DNMT1):c.*274T>C rs886054125
NM_001130823.3(DNMT1):c.-34C>G rs112908248
NM_001130823.3(DNMT1):c.1009-8C>G rs766626750
NM_001130823.3(DNMT1):c.1044-18dup rs59599980
NM_001130823.3(DNMT1):c.1044-8del rs59599980
NM_001130823.3(DNMT1):c.1044-9_1044-8del rs59599980
NM_001130823.3(DNMT1):c.1224C>T (p.Asn408=) rs199584370
NM_001130823.3(DNMT1):c.1389A>G (p.Pro463=) rs2228611
NM_001130823.3(DNMT1):c.1436A>C (p.Glu479Ala) rs374027926
NM_001130823.3(DNMT1):c.1500C>T (p.Ala500=) rs75443147
NM_001130823.3(DNMT1):c.150C>T (p.His50=) rs146112081
NM_001130823.3(DNMT1):c.1632C>A (p.Ile544=) rs2228613
NM_001130823.3(DNMT1):c.1782A>G (p.Thr594=) rs721186
NM_001130823.3(DNMT1):c.1832+14A>G rs2114724
NM_001130823.3(DNMT1):c.1861A>C (p.Arg621=) rs144567470
NM_001130823.3(DNMT1):c.1932C>T (p.Phe644=) rs370444117
NM_001130823.3(DNMT1):c.1944C>T (p.Phe648=) rs61750052
NM_001130823.3(DNMT1):c.2019+15G>C rs370849760
NM_001130823.3(DNMT1):c.2020-10C>T rs369373339
NM_001130823.3(DNMT1):c.206G>A (p.Arg69His) rs61750053
NM_001130823.3(DNMT1):c.2117+13G>A rs112660071
NM_001130823.3(DNMT1):c.2260G>A (p.Val754Ile) rs762172122
NM_001130823.3(DNMT1):c.2382-4C>T rs74505694
NM_001130823.3(DNMT1):c.2463C>T (p.Leu821=) rs61750051
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792
NM_001130823.3(DNMT1):c.2626G>A (p.Gly876Arg) rs62621087
NM_001130823.3(DNMT1):c.2693C>T (p.Thr898Ile) rs201213597
NM_001130823.3(DNMT1):c.2807G>A (p.Arg936Gln) rs763321599
NM_001130823.3(DNMT1):c.290A>G (p.His97Arg) rs16999593
NM_001130823.3(DNMT1):c.3117-8G>A rs769623856
NM_001130823.3(DNMT1):c.3343C>T (p.Pro1115Ser) rs755865204
NM_001130823.3(DNMT1):c.3351C>T (p.Asn1117=) rs534263445
NM_001130823.3(DNMT1):c.3394+7C>T rs886054128
NM_001130823.3(DNMT1):c.3408C>G (p.Pro1136=) rs144675407
NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys) rs201308454
NM_001130823.3(DNMT1):c.358G>C (p.Val120Leu) rs75616428
NM_001130823.3(DNMT1):c.3696C>T (p.Asp1232=) rs145657360
NM_001130823.3(DNMT1):c.387C>T (p.Pro129=) rs369470867
NM_001130823.3(DNMT1):c.3936C>T (p.Phe1312=) rs367637414
NM_001130823.3(DNMT1):c.3939C>T (p.Gly1313=) rs142903301
NM_001130823.3(DNMT1):c.393C>T (p.Pro131=) rs143904813
NM_001130823.3(DNMT1):c.3948+4G>A rs774356396
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys) rs138841970
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699
NM_001130823.3(DNMT1):c.4146G>A (p.Thr1382=) rs184125970
NM_001130823.3(DNMT1):c.4204A>T (p.Ile1402Phe) rs886054127
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.3(DNMT1):c.4554C>T (p.His1518=) rs753248212
NM_001130823.3(DNMT1):c.4657-15G>A rs201805582
NM_001130823.3(DNMT1):c.483T>C (p.Thr161=) rs764496230
NM_001130823.3(DNMT1):c.4876G>A (p.Glu1626Lys) rs201774098
NM_001130823.3(DNMT1):c.4894G>C (p.Asp1632His) rs147118268
NM_001130823.3(DNMT1):c.493+8C>T rs138998574
NM_001130823.3(DNMT1):c.500C>G (p.Pro167Arg) rs886054129
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val) rs62621089
NM_001130823.3(DNMT1):c.633A>G (p.Glu211=) rs141264613
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu) rs150999369
NM_001130823.3(DNMT1):c.768+12T>A rs189898346
NM_001130823.3(DNMT1):c.891+8C>T rs117294281
NM_001130823.3(DNMT1):c.916C>T (p.Pro306Ser) rs761747950
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044
NM_001130823.3(DNMT1):c.979A>G (p.Ile327Val) rs2228612
NM_001130823.3(DNMT1):c.981T>G (p.Ile327Met) rs61758431
NM_001130823.3(DNMT1):c.996C>T (p.Asp332=) rs16999358

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