ClinVar Miner

List of variants in gene DNMT1 reported as likely benign for Dementia, Deafness, and Sensory Neuropathy

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Total variants: 35
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HGVS dbSNP
NM_001130823.2(DNMT1):c.*323C>G rs146694575
NM_001130823.2(DNMT1):c.-72C>T rs779334757
NM_001130823.3(DNMT1):c.*165T>G rs192952800
NM_001130823.3(DNMT1):c.1224C>T (p.Asn408=) rs199584370
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.1861A>C (p.Arg621=) rs144567470
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.2117+13G>A rs112660071
NM_001130823.3(DNMT1):c.2382-4C>T rs74505694
NM_001130823.3(DNMT1):c.2463C>T (p.Leu821=) rs61750051
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792
NM_001130823.3(DNMT1):c.2626G>A (p.Gly876Arg) rs62621087
NM_001130823.3(DNMT1):c.2693C>T (p.Thr898Ile) rs201213597
NM_001130823.3(DNMT1):c.3351C>T (p.Asn1117=) rs534263445
NM_001130823.3(DNMT1):c.3408C>G (p.Pro1136=) rs144675407
NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys) rs201308454
NM_001130823.3(DNMT1):c.3696C>T (p.Asp1232=) rs145657360
NM_001130823.3(DNMT1):c.3939C>T (p.Gly1313=) rs142903301
NM_001130823.3(DNMT1):c.393C>T (p.Pro131=) rs143904813
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys) rs138841970
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699
NM_001130823.3(DNMT1):c.4146G>A (p.Thr1382=) rs184125970
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.3(DNMT1):c.4554C>T (p.His1518=) rs753248212
NM_001130823.3(DNMT1):c.4657-15G>A rs201805582
NM_001130823.3(DNMT1):c.493+8C>T rs138998574
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val) rs62621089
NM_001130823.3(DNMT1):c.633A>G (p.Glu211=) rs141264613
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu) rs150999369
NM_001130823.3(DNMT1):c.768+12T>A rs189898346
NM_001130823.3(DNMT1):c.891+8C>T rs117294281
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044
NM_001130823.3(DNMT1):c.981T>G (p.Ile327Met) rs61758431

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