ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044 0.00011
NM_001130823.3(DNMT1):c.520A>C (p.Thr174Pro) rs201319352 0.00009
NM_001130823.3(DNMT1):c.1066G>A (p.Ala356Thr) rs529074384 0.00006
NM_001130823.3(DNMT1):c.1861A>C (p.Arg621=) rs144567470 0.00006
NM_001130823.3(DNMT1):c.3696C>T (p.Asp1232=) rs145657360 0.00006
NM_001130823.3(DNMT1):c.1932C>T (p.Phe644=) rs370444117 0.00005
NM_001130823.3(DNMT1):c.2019+15G>C rs370849760 0.00005
NM_001130823.3(DNMT1):c.4894G>C (p.Asp1632His) rs147118268 0.00005
NM_001130823.3(DNMT1):c.1436A>C (p.Glu479Ala) rs374027926 0.00004
NM_001130823.3(DNMT1):c.3116+11G>T rs773580930 0.00004
NM_001130823.3(DNMT1):c.4173G>A (p.Pro1391=) rs550868730 0.00004
NM_001130823.3(DNMT1):c.1149T>C (p.Tyr383=) rs766807027 0.00002
NM_001130823.3(DNMT1):c.1842G>A (p.Gln614=) rs756623224 0.00001
NM_001130823.3(DNMT1):c.2260G>A (p.Val754Ile) rs762172122 0.00001
NM_001130823.3(DNMT1):c.3036C>G (p.Ile1012Met) rs376854079 0.00001
NM_001130823.3(DNMT1):c.*18C>A rs778467461
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699

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