ClinVar Miner

List of variants in gene DNMT1 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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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.1500C>T (p.Ala500=) rs75443147 0.00552
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_001130823.2(DNMT1):c.*323C>G rs146694575 0.00273
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321 0.00251
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.2117+13G>A rs112660071 0.00153
NM_001130823.3(DNMT1):c.768+12T>A rs189898346 0.00123
NM_001130823.3(DNMT1):c.493+8C>T rs138998574 0.00107
NM_001130823.3(DNMT1):c.*287T>C rs189422259 0.00098
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792 0.00067
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu) rs150999369 0.00066
NM_001130823.3(DNMT1):c.981T>G (p.Ile327Met) rs61758431 0.00039
NM_001130823.3(DNMT1):c.2626G>A (p.Gly876Arg) rs62621087 0.00038
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.393C>T (p.Pro131=) rs143904813 0.00024
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys) rs138841970 0.00024
NM_001130823.3(DNMT1):c.2693C>T (p.Thr898Ile) rs201213597 0.00023
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val) rs62621089 0.00023
NM_001130823.3(DNMT1):c.387C>T (p.Pro129=) rs369470867 0.00019
NM_001130823.3(DNMT1):c.4146G>A (p.Thr1382=) rs184125970 0.00017
NM_001130823.3(DNMT1):c.633A>G (p.Glu211=) rs141264613 0.00017
NM_001130823.3(DNMT1):c.1896G>A (p.Thr632=) rs202058239 0.00016
NM_001130823.3(DNMT1):c.2020-10C>T rs369373339 0.00014
NM_001130823.3(DNMT1):c.382C>A (p.Pro128Thr) rs146601335 0.00013
NM_001130823.3(DNMT1):c.4876G>A (p.Glu1626Lys) rs201774098 0.00011
NM_001130823.3(DNMT1):c.868G>A (p.Glu290Lys) rs200024502 0.00011
NM_001130823.3(DNMT1):c.2914G>A (p.Val972Met) rs148038464 0.00009
NM_001130823.3(DNMT1):c.3936C>T (p.Phe1312=) rs367637414 0.00007
NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys) rs201308454 0.00006
NM_001130823.3(DNMT1):c.3669C>T (p.Arg1223=) rs147755768 0.00006
NM_001130823.3(DNMT1):c.3351C>T (p.Asn1117=) rs534263445 0.00005
NM_001130823.2(DNMT1):c.-72C>T rs779334757 0.00004
NM_001130823.3(DNMT1):c.3668G>A (p.Arg1223His) rs757460628 0.00001
NM_001130823.3(DNMT1):c.4860C>T (p.Ala1620=) rs576877219 0.00001
NM_001130823.3(DNMT1):c.1009-8C>G rs766626750
NM_001130823.3(DNMT1):c.1044-8del rs59599980
NM_001130823.3(DNMT1):c.1044-9_1044-8del rs59599980
NM_001130823.3(DNMT1):c.3948+4G>A rs774356396

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