ClinVar Miner

List of variants in gene DNMT1 reported as benign for Hereditary sensory neuropathy type IE

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Total variants: 20
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HGVS dbSNP
NM_001130823.3(DNMT1):c.1095C>T (p.His365=) rs116502459
NM_001130823.3(DNMT1):c.1206G>C (p.Leu402=) rs147235870
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.1845G>A (p.Ala615=) rs761852984
NM_001130823.3(DNMT1):c.1944C>T (p.Phe648=) rs61750052
NM_001130823.3(DNMT1):c.206G>A (p.Arg69His) rs61750053
NM_001130823.3(DNMT1):c.2382-4C>T rs74505694
NM_001130823.3(DNMT1):c.2463C>T (p.Leu821=) rs61750051
NM_001130823.3(DNMT1):c.290A>G (p.His97Arg) rs16999593
NM_001130823.3(DNMT1):c.3492C>T (p.Cys1164=) rs140951214
NM_001130823.3(DNMT1):c.358G>C (p.Val120Leu) rs75616428
NM_001130823.3(DNMT1):c.3939C>T (p.Gly1313=) rs142903301
NM_001130823.3(DNMT1):c.4368C>T (p.Pro1456=) rs2229858
NM_001130823.3(DNMT1):c.4503C>T (p.Cys1501=) rs149271718
NM_001130823.3(DNMT1):c.4860C>T (p.Ala1620=) rs576877219
NM_001130823.3(DNMT1):c.633A>G (p.Glu211=) rs141264613
NM_001130823.3(DNMT1):c.891+8C>T rs117294281
NM_001130823.3(DNMT1):c.925C>G (p.Leu309Val) rs61758430
NM_001130823.3(DNMT1):c.996C>T (p.Asp332=) rs16999358

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