ClinVar Miner

List of variants in gene DNMT1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_001130823.3(DNMT1):c.*126A>G rs886054126
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.1436A>C (p.Glu479Ala) rs374027926
NM_001130823.3(DNMT1):c.1932C>T (p.Phe644=) rs370444117
NM_001130823.3(DNMT1):c.2019+15G>C rs370849760
NM_001130823.3(DNMT1):c.2020-10C>T rs369373339
NM_001130823.3(DNMT1):c.2260G>A (p.Val754Ile) rs762172122
NM_001130823.3(DNMT1):c.2807G>A (p.Arg936Gln) rs763321599
NM_001130823.3(DNMT1):c.3117-8G>A rs769623856
NM_001130823.3(DNMT1):c.3343C>T (p.Pro1115Ser) rs755865204
NM_001130823.3(DNMT1):c.3394+7C>T rs886054128
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.3948+4G>A rs774356396
NM_001130823.3(DNMT1):c.4204A>T (p.Ile1402Phe) rs886054127
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.500C>G (p.Pro167Arg) rs886054129
NM_001130823.3(DNMT1):c.916C>T (p.Pro306Ser) rs761747950

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