ClinVar Miner

List of variants in gene DNMT1 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_001130823.1(DNMT1):c.206G>A (p.Arg69His) rs61750053
NM_001130823.1(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.2(DNMT1):c.1095C>T (p.His365=) rs116502459
NM_001130823.2(DNMT1):c.1389A>G (p.Pro463=) rs2228611
NM_001130823.2(DNMT1):c.1500C>T (p.Ala500=) rs75443147
NM_001130823.2(DNMT1):c.150C>T (p.His50=) rs146112081
NM_001130823.2(DNMT1):c.1632C>A (p.Ile544=) rs2228613
NM_001130823.2(DNMT1):c.1782A>G (p.Thr594=) rs721186
NM_001130823.2(DNMT1):c.1832+14A>G rs2114724
NM_001130823.2(DNMT1):c.1944C>T (p.Phe648=) rs61750052
NM_001130823.2(DNMT1):c.2117+13G>A rs112660071
NM_001130823.2(DNMT1):c.2382-4C>T rs74505694
NM_001130823.2(DNMT1):c.2676C>T (p.Phe892=) rs139861062
NM_001130823.2(DNMT1):c.290A>G (p.His97Arg) rs16999593
NM_001130823.2(DNMT1):c.3939C>T (p.Gly1313=) rs142903301
NM_001130823.2(DNMT1):c.393C>T (p.Pro131=) rs143904813
NM_001130823.2(DNMT1):c.4294-17C>A rs79585069
NM_001130823.2(DNMT1):c.4294-19G>C rs2290683
NM_001130823.2(DNMT1):c.891+8C>T rs117294281
NM_001130823.2(DNMT1):c.979A>G (p.Ile327Val) rs2228612

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