ClinVar Miner

List of variants in gene DNMT1 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_001130823.3(DNMT1):c.1058T>C (p.Met353Thr) rs544428951
NM_001130823.3(DNMT1):c.1080G>A (p.Met360Ile) rs1064796441
NM_001130823.3(DNMT1):c.1535C>T (p.Ala512Val) rs1064796687
NM_001130823.3(DNMT1):c.1743_1746del (p.Asp581fs) rs879253953
NM_001130823.3(DNMT1):c.1850G>A (p.Arg617Gln) rs751902349
NM_001130823.3(DNMT1):c.2315C>A (p.Thr772Asn) rs142562681
NM_001130823.3(DNMT1):c.2602G>A (p.Glu868Lys) rs761717775
NM_001130823.3(DNMT1):c.2689A>G (p.Lys897Glu) rs746143694
NM_001130823.3(DNMT1):c.2693C>T (p.Thr898Ile) rs201213597
NM_001130823.3(DNMT1):c.2836G>A (p.Gly946Ser) rs777416084
NM_001130823.3(DNMT1):c.3031C>T (p.Arg1011Trp) rs876661227
NM_001130823.3(DNMT1):c.3232G>A (p.Val1078Met) rs560179619
NM_001130823.3(DNMT1):c.3283G>A (p.Gly1095Ser) rs747265409
NM_001130823.3(DNMT1):c.3353A>G (p.His1118Arg) rs150331990
NM_001130823.3(DNMT1):c.341G>A (p.Arg114Lys) rs554894511
NM_001130823.3(DNMT1):c.3519A>C (p.Gln1173His) rs151305495
NM_001130823.3(DNMT1):c.368C>G (p.Ala123Gly) rs1085307725
NM_001130823.3(DNMT1):c.382C>A (p.Pro128Thr) rs146601335
NM_001130823.3(DNMT1):c.385C>A (p.Pro129Thr) rs1085307715
NM_001130823.3(DNMT1):c.4001C>T (p.Ala1334Val) rs766051225
NM_001130823.3(DNMT1):c.4255G>A (p.Ala1419Thr) rs374047326
NM_001130823.3(DNMT1):c.4444C>T (p.Arg1482Cys) rs147984942
NM_001130823.3(DNMT1):c.4876G>A (p.Glu1626Lys) rs201774098
NM_001130823.3(DNMT1):c.56C>T (p.Ser19Leu) rs747559452
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val) rs62621089
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu) rs150999369
NM_001130823.3(DNMT1):c.856G>A (p.Val286Met) rs368960099
NM_001130823.3(DNMT1):c.868G>A (p.Glu290Lys) rs200024502
NM_001130823.3(DNMT1):c.919A>G (p.Lys307Glu) rs148831705

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