ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_001130823.3(DNMT1):c.382C>A (p.Pro128Thr) rs146601335 0.00013
NM_001130823.3(DNMT1):c.2315C>A (p.Thr772Asn) rs142562681 0.00010
NM_001130823.3(DNMT1):c.1987G>A (p.Ala663Thr) rs146467216 0.00007
NM_001130823.3(DNMT1):c.3261C>T (p.Cys1087=) rs374021326 0.00007
NM_001130823.3(DNMT1):c.4444C>T (p.Arg1482Cys) rs147984942 0.00006
NM_001130823.3(DNMT1):c.1678C>T (p.Arg560Cys) rs375474222 0.00005
NM_001130823.3(DNMT1):c.3232G>A (p.Val1078Met) rs560179619 0.00005
NM_001130823.3(DNMT1):c.1436A>C (p.Glu479Ala) rs374027926 0.00004
NM_001130823.3(DNMT1):c.2836G>A (p.Gly946Ser) rs777416084 0.00004
NM_001130823.3(DNMT1):c.3157G>A (p.Ala1053Thr) rs370786558 0.00004
NM_001130823.3(DNMT1):c.4236C>G (p.Phe1412Leu) rs766558026 0.00004
NM_001130823.3(DNMT1):c.4324C>T (p.Arg1442Trp) rs139918621 0.00004
NM_001130823.3(DNMT1):c.1613C>T (p.Ser538Leu) rs1037636262 0.00003
NM_001130823.3(DNMT1):c.2602G>A (p.Glu868Lys) rs761717775 0.00003
NM_001130823.3(DNMT1):c.2741G>A (p.Arg914His) rs756944531 0.00003
NM_001130823.3(DNMT1):c.855C>T (p.Gly285=) rs755151805 0.00003
NM_001130823.3(DNMT1):c.1850G>A (p.Arg617Gln) rs751902349 0.00002
NM_001130823.3(DNMT1):c.2689A>G (p.Lys897Glu) rs746143694 0.00002
NM_001130823.3(DNMT1):c.2950C>A (p.Leu984Met) rs760683699 0.00002
NM_001130823.3(DNMT1):c.3353A>G (p.His1118Arg) rs150331990 0.00002
NM_001130823.3(DNMT1):c.3519A>C (p.Gln1173His) rs151305495 0.00002
NM_001130823.3(DNMT1):c.3595G>A (p.Gly1199Ser) rs780717834 0.00002
NM_001130823.3(DNMT1):c.4255G>A (p.Ala1419Thr) rs374047326 0.00002
NM_001130823.3(DNMT1):c.430G>A (p.Asp144Asn) rs765353997 0.00002
NM_001130823.3(DNMT1):c.1058T>C (p.Met353Thr) rs544428951 0.00001
NM_001130823.3(DNMT1):c.1972G>C (p.Glu658Gln) rs756254318 0.00001
NM_001130823.3(DNMT1):c.2011G>A (p.Val671Ile) rs1486893166 0.00001
NM_001130823.3(DNMT1):c.2260G>A (p.Val754Ile) rs762172122 0.00001
NM_001130823.3(DNMT1):c.2569G>A (p.Glu857Lys) rs751754286 0.00001
NM_001130823.3(DNMT1):c.3031C>T (p.Arg1011Trp) rs876661227 0.00001
NM_001130823.3(DNMT1):c.3184G>A (p.Asp1062Asn) rs548883904 0.00001
NM_001130823.3(DNMT1):c.3283G>A (p.Gly1095Ser) rs747265409 0.00001
NM_001130823.3(DNMT1):c.341G>A (p.Arg114Lys) rs554894511 0.00001
NM_001130823.3(DNMT1):c.3667C>T (p.Arg1223Cys) rs779029407 0.00001
NM_001130823.3(DNMT1):c.368C>G (p.Ala123Gly) rs1085307725 0.00001
NM_001130823.3(DNMT1):c.4000G>A (p.Ala1334Thr) rs779967013 0.00001
NM_001130823.3(DNMT1):c.4001C>T (p.Ala1334Val) rs766051225 0.00001
NM_001130823.3(DNMT1):c.4193C>T (p.Ser1398Leu) rs375225009 0.00001
NM_001130823.3(DNMT1):c.4891A>G (p.Lys1631Glu) rs1004658637 0.00001
NM_001130823.3(DNMT1):c.803C>T (p.Pro268Leu) rs779634956 0.00001
NM_001130823.3(DNMT1):c.997G>A (p.Glu333Lys) rs748515801 0.00001
NM_001130823.3(DNMT1):c.1070A>G (p.Lys357Arg)
NM_001130823.3(DNMT1):c.1080G>A (p.Met360Ile) rs1064796441
NM_001130823.3(DNMT1):c.1280+2T>C
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.1829A>G (p.Gln610Arg)
NM_001130823.3(DNMT1):c.1880A>G (p.Lys627Arg)
NM_001130823.3(DNMT1):c.1931T>G (p.Phe644Cys) rs2145307324
NM_001130823.3(DNMT1):c.223G>A (p.Glu75Lys) rs1206145138
NM_001130823.3(DNMT1):c.2390C>T (p.Ala797Val)
NM_001130823.3(DNMT1):c.2630A>G (p.Lys877Arg) rs2145291695
NM_001130823.3(DNMT1):c.2801A>C (p.Asp934Ala)
NM_001130823.3(DNMT1):c.2851G>A (p.Val951Ile) rs2145283133
NM_001130823.3(DNMT1):c.3013G>A (p.Glu1005Lys) rs747897637
NM_001130823.3(DNMT1):c.3139A>G (p.Thr1047Ala) rs751674187
NM_001130823.3(DNMT1):c.3176A>G (p.Tyr1059Cys)
NM_001130823.3(DNMT1):c.3209A>G (p.Lys1070Arg) rs1426702144
NM_001130823.3(DNMT1):c.3294C>G (p.Arg1098=) rs775786809
NM_001130823.3(DNMT1):c.3343C>G (p.Pro1115Ala) rs755865204
NM_001130823.3(DNMT1):c.3363C>G (p.Ser1121Arg)
NM_001130823.3(DNMT1):c.3509G>T (p.Gly1170Val) rs2145267014
NM_001130823.3(DNMT1):c.3656C>T (p.Thr1219Ile) rs201497993
NM_001130823.3(DNMT1):c.3670G>A (p.Gly1224Ser)
NM_001130823.3(DNMT1):c.3678G>A (p.Arg1226=)
NM_001130823.3(DNMT1):c.373G>A (p.Ala125Thr)
NM_001130823.3(DNMT1):c.385C>A (p.Pro129Thr) rs1085307715
NM_001130823.3(DNMT1):c.4845A>T (p.Lys1615Asn) rs2089433358
NM_001130823.3(DNMT1):c.4896C>G (p.Asp1632Glu)
NM_001130823.3(DNMT1):c.490A>G (p.Arg164Gly) rs2145377808
NM_001130823.3(DNMT1):c.494-4A>G
NM_001130823.3(DNMT1):c.570-7G>A rs2145365826
NM_001130823.3(DNMT1):c.726A>C (p.Lys242Asn) rs2145359310
NM_001130823.3(DNMT1):c.833C>G (p.Pro278Arg)
NM_001130823.3(DNMT1):c.856G>C (p.Val286Leu) rs368960099
NM_001130823.3(DNMT1):c.859C>G (p.Gln287Glu) rs2145340495

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