ClinVar Miner

List of variants in gene DNMT1 studied for not provided

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Gene type:
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Total variants: 76
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HGVS dbSNP
NC_000019.10:g.10146214_10146215del
NM_001130823.3(DNMT1):c.1008+26C>T
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.1287C>T (p.Tyr429=) rs536069799
NM_001130823.3(DNMT1):c.1303C>G (p.Leu435Val) rs1555691714
NM_001130823.3(DNMT1):c.1314C>T (p.Ile438=)
NM_001130823.3(DNMT1):c.1492+30G>A
NM_001130823.3(DNMT1):c.150C>T (p.His50=) rs146112081
NM_001130823.3(DNMT1):c.1531T>C (p.Tyr511His) rs199473692
NM_001130823.3(DNMT1):c.1532A>G (p.Tyr511Cys) rs199473690
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.2020-289C>A
NM_001130823.3(DNMT1):c.206G>A (p.Arg69His) rs61750053
NM_001130823.3(DNMT1):c.2268T>C (p.Thr756=) rs374841430
NM_001130823.3(DNMT1):c.2315C>A (p.Thr772Asn) rs142562681
NM_001130823.3(DNMT1):c.2387C>T (p.Thr796Met) rs148987580
NM_001130823.3(DNMT1):c.2586+45G>A
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.2721-10T>A rs377355204
NM_001130823.3(DNMT1):c.2721-45C>T
NM_001130823.3(DNMT1):c.2728G>T (p.Val910Leu) rs150863675
NM_001130823.3(DNMT1):c.2835C>T (p.Asn945=) rs539948794
NM_001130823.3(DNMT1):c.2836G>A (p.Gly946Ser) rs777416084
NM_001130823.3(DNMT1):c.2914G>A (p.Val972Met) rs148038464
NM_001130823.3(DNMT1):c.2937C>T (p.Pro979=)
NM_001130823.3(DNMT1):c.2950C>A (p.Leu984Met)
NM_001130823.3(DNMT1):c.3031C>T (p.Arg1011Trp) rs876661227
NM_001130823.3(DNMT1):c.3116+327C>T
NM_001130823.3(DNMT1):c.3117-203A>C
NM_001130823.3(DNMT1):c.3117-288T>C
NM_001130823.3(DNMT1):c.3156C>T (p.His1052=) rs141856197
NM_001130823.3(DNMT1):c.3196G>A (p.Val1066Met) rs187394074
NM_001130823.3(DNMT1):c.3224G>A (p.Arg1075His) rs779489678
NM_001130823.3(DNMT1):c.327C>T (p.Asn109=)
NM_001130823.3(DNMT1):c.3283G>A (p.Gly1095Ser) rs747265409
NM_001130823.3(DNMT1):c.3310-133T>C
NM_001130823.3(DNMT1):c.3353A>G (p.His1118Arg) rs150331990
NM_001130823.3(DNMT1):c.3394+34T>C
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.3523+90C>G
NM_001130823.3(DNMT1):c.3523+9C>T rs886043812
NM_001130823.3(DNMT1):c.368C>G (p.Ala123Gly) rs1085307725
NM_001130823.3(DNMT1):c.3767A>G (p.Tyr1256Cys) rs1085307800
NM_001130823.3(DNMT1):c.3806+6C>T rs371779379
NM_001130823.3(DNMT1):c.385C>A (p.Pro129Thr) rs1085307715
NM_001130823.3(DNMT1):c.3949-5C>G rs773047717
NM_001130823.3(DNMT1):c.4001C>T (p.Ala1334Val) rs766051225
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699
NM_001130823.3(DNMT1):c.4193C>T (p.Ser1398Leu) rs375225009
NM_001130823.3(DNMT1):c.4255G>A (p.Ala1419Thr) rs374047326
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.3(DNMT1):c.4444C>T (p.Arg1482Cys) rs147984942
NM_001130823.3(DNMT1):c.4554C>T (p.His1518=) rs753248212
NM_001130823.3(DNMT1):c.4626C>T (p.Thr1542=)
NM_001130823.3(DNMT1):c.469G>A (p.Ala157Thr) rs886044275
NM_001130823.3(DNMT1):c.4865-154G>A
NM_001130823.3(DNMT1):c.4876G>A (p.Glu1626Lys) rs201774098
NM_001130823.3(DNMT1):c.569+126C>T
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val) rs62621089
NM_001130823.3(DNMT1):c.614C>T (p.Ser205Leu)
NM_001130823.3(DNMT1):c.649-197T>C
NM_001130823.3(DNMT1):c.649-62G>A
NM_001130823.3(DNMT1):c.734C>T (p.Thr245Met) rs143598088
NM_001130823.3(DNMT1):c.769-149A>G
NM_001130823.3(DNMT1):c.804-57C>T
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.892-84G>A
NM_001130823.3(DNMT1):c.919A>G (p.Lys307Glu) rs148831705
NM_001130823.3(DNMT1):c.926+10T>G rs886044170
NM_001130823.3(DNMT1):c.950A>G (p.Glu317Gly) rs1478185698

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