ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 99
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HGVS dbSNP
NM_001130823.3(DNMT1):c.1043C>T (p.Pro348Leu)
NM_001130823.3(DNMT1):c.1051A>G (p.Lys351Glu)
NM_001130823.3(DNMT1):c.1064G>A (p.Arg355His) rs201945078
NM_001130823.3(DNMT1):c.1066G>A (p.Ala356Thr) rs529074384
NM_001130823.3(DNMT1):c.1066G>T (p.Ala356Ser)
NM_001130823.3(DNMT1):c.1108A>C (p.Ile370Leu) rs1316802867
NM_001130823.3(DNMT1):c.1170+5G>C
NM_001130823.3(DNMT1):c.118-7C>G
NM_001130823.3(DNMT1):c.1196A>G (p.Asn399Ser)
NM_001130823.3(DNMT1):c.1281T>C (p.Ser427=) rs1555691724
NM_001130823.3(DNMT1):c.1378G>C (p.Asp460His) rs1403539644
NM_001130823.3(DNMT1):c.1393C>G (p.Leu465Val)
NM_001130823.3(DNMT1):c.1394T>C (p.Leu465Pro)
NM_001130823.3(DNMT1):c.1642G>A (p.Glu548Lys)
NM_001130823.3(DNMT1):c.1645-10C>A rs752563425
NM_001130823.3(DNMT1):c.1983G>T (p.Glu661Asp)
NM_001130823.3(DNMT1):c.1987G>A (p.Ala663Thr)
NM_001130823.3(DNMT1):c.2018A>G (p.Glu673Gly) rs1555691311
NM_001130823.3(DNMT1):c.2030A>G (p.Gln677Arg) rs1568232544
NM_001130823.3(DNMT1):c.2068G>A (p.Val690Ile) rs1568232526
NM_001130823.3(DNMT1):c.2108A>G (p.Gln703Arg)
NM_001130823.3(DNMT1):c.2113C>T (p.Arg705Trp)
NM_001130823.3(DNMT1):c.2211_2213GAA[5] (p.Lys741dup)
NM_001130823.3(DNMT1):c.225+4A>G rs1265807438
NM_001130823.3(DNMT1):c.229G>A (p.Gly77Ser)
NM_001130823.3(DNMT1):c.2366C>T (p.Pro789Leu)
NM_001130823.3(DNMT1):c.2377G>T (p.Ala793Ser) rs1223065154
NM_001130823.3(DNMT1):c.2383G>A (p.Val795Ile) rs1555690511
NM_001130823.3(DNMT1):c.2387C>T (p.Thr796Met) rs148987580
NM_001130823.3(DNMT1):c.2474C>T (p.Ser825Leu) rs1555690467
NM_001130823.3(DNMT1):c.2689A>G (p.Lys897Glu) rs746143694
NM_001130823.3(DNMT1):c.2711A>T (p.Asn904Ile)
NM_001130823.3(DNMT1):c.2721-10T>A rs377355204
NM_001130823.3(DNMT1):c.2728G>T (p.Val910Leu) rs150863675
NM_001130823.3(DNMT1):c.2794G>A (p.Asp932Asn) rs910412179
NM_001130823.3(DNMT1):c.2836G>A (p.Gly946Ser) rs777416084
NM_001130823.3(DNMT1):c.2836G>T (p.Gly946Cys)
NM_001130823.3(DNMT1):c.2888C>T (p.Thr963Met)
NM_001130823.3(DNMT1):c.2914G>A (p.Val972Met) rs148038464
NM_001130823.3(DNMT1):c.2926C>T (p.Arg976Trp) rs1568226455
NM_001130823.3(DNMT1):c.299A>G (p.Asn100Ser) rs1375073063
NM_001130823.3(DNMT1):c.301C>T (p.Arg101Trp)
NM_001130823.3(DNMT1):c.302G>A (p.Arg101Gln) rs1401130665
NM_001130823.3(DNMT1):c.3116+3C>G
NM_001130823.3(DNMT1):c.316C>T (p.Arg106Cys) rs759600542
NM_001130823.3(DNMT1):c.3223C>T (p.Arg1075Cys)
NM_001130823.3(DNMT1):c.3232G>A (p.Val1078Met) rs560179619
NM_001130823.3(DNMT1):c.3262G>A (p.Val1088Ile) rs776461147
NM_001130823.3(DNMT1):c.328G>A (p.Gly110Arg) rs376894659
NM_001130823.3(DNMT1):c.3293G>A (p.Arg1098His)
NM_001130823.3(DNMT1):c.3352C>T (p.His1118Tyr)
NM_001130823.3(DNMT1):c.3353A>G (p.His1118Arg) rs150331990
NM_001130823.3(DNMT1):c.3401G>A (p.Gly1134Asp)
NM_001130823.3(DNMT1):c.341G>A (p.Arg114Lys) rs554894511
NM_001130823.3(DNMT1):c.3498G>T (p.Gly1166=) rs1186008456
NM_001130823.3(DNMT1):c.3519A>C (p.Gln1173His) rs151305495
NM_001130823.3(DNMT1):c.3523+6C>T rs372240993
NM_001130823.3(DNMT1):c.3668G>A (p.Arg1223His) rs757460628
NM_001130823.3(DNMT1):c.382C>A (p.Pro128Thr) rs146601335
NM_001130823.3(DNMT1):c.382C>T (p.Pro128Ser) rs146601335
NM_001130823.3(DNMT1):c.3830G>A (p.Arg1277Gln)
NM_001130823.3(DNMT1):c.3901C>T (p.Arg1301Cys)
NM_001130823.3(DNMT1):c.3909G>A (p.Leu1303=)
NM_001130823.3(DNMT1):c.4032G>A (p.Pro1344=) rs150774582
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys) rs138841970
NM_001130823.3(DNMT1):c.407G>A (p.Arg136His) rs775139340
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699
NM_001130823.3(DNMT1):c.4181G>A (p.Arg1394Gln)
NM_001130823.3(DNMT1):c.4193C>T (p.Ser1398Leu) rs375225009
NM_001130823.3(DNMT1):c.4216G>A (p.Gly1406Arg) rs1568220739
NM_001130823.3(DNMT1):c.4293+5T>C rs199506146
NM_001130823.3(DNMT1):c.4327C>A (p.His1443Asn) rs1255037718
NM_001130823.3(DNMT1):c.4427A>G (p.His1476Arg) rs765347113
NM_001130823.3(DNMT1):c.4483G>A (p.Val1495Met) rs781301028
NM_001130823.3(DNMT1):c.451A>G (p.Arg151Gly)
NM_001130823.3(DNMT1):c.4739G>A (p.Arg1580Gln) rs1568218498
NM_001130823.3(DNMT1):c.4741C>T (p.Leu1581Phe) rs1568218491
NM_001130823.3(DNMT1):c.4819G>A (p.Glu1607Lys) rs1568217087
NM_001130823.3(DNMT1):c.526A>C (p.Lys176Gln)
NM_001130823.3(DNMT1):c.527A>G (p.Lys176Arg)
NM_001130823.3(DNMT1):c.56C>T (p.Ser19Leu) rs747559452
NM_001130823.3(DNMT1):c.63C>A (p.Pro21=) rs1245074338
NM_001130823.3(DNMT1):c.650A>G (p.Asp217Gly) rs1568249130
NM_001130823.3(DNMT1):c.692G>A (p.Arg231Lys)
NM_001130823.3(DNMT1):c.695C>T (p.Pro232Leu)
NM_001130823.3(DNMT1):c.734C>T (p.Thr245Met) rs143598088
NM_001130823.3(DNMT1):c.737G>A (p.Arg246His) rs771381056
NM_001130823.3(DNMT1):c.78G>C (p.Arg26Ser) rs780503694
NM_001130823.3(DNMT1):c.803C>T (p.Pro268Leu)
NM_001130823.3(DNMT1):c.856G>A (p.Val286Met) rs368960099
NM_001130823.3(DNMT1):c.857T>C (p.Val286Ala)
NM_001130823.3(DNMT1):c.874G>A (p.Glu292Lys) rs1257025095
NM_001130823.3(DNMT1):c.890A>G (p.Lys297Arg) rs201025441
NM_001130823.3(DNMT1):c.894_896del (p.Asp298del) rs1568241116
NM_001130823.3(DNMT1):c.898A>C (p.Lys300Gln)
NM_001130823.3(DNMT1):c.919A>G (p.Lys307Glu) rs148831705
NM_001130823.3(DNMT1):c.931G>T (p.Ala311Ser)
NM_001130823.3(DNMT1):c.938G>A (p.Arg313Gln)
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044

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