ClinVar Miner

List of variants in gene DNMT1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_001130823.3(DNMT1):c.2463C>T (p.Leu821=) rs61750051 0.00377
NM_001130823.3(DNMT1):c.891+8C>T rs117294281 0.00299
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321 0.00251
NM_001130823.3(DNMT1):c.150C>T (p.His50=) rs146112081 0.00182
NM_001130823.3(DNMT1):c.1206G>C (p.Leu402=) rs147235870 0.00163
NM_001130823.3(DNMT1):c.*165T>G rs192952800 0.00132
NM_001130823.3(DNMT1):c.2676C>T (p.Phe892=) rs139861062 0.00108
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792 0.00067
NM_001130823.3(DNMT1):c.981T>G (p.Ile327Met) rs61758431 0.00039
NM_001130823.3(DNMT1):c.1224C>T (p.Asn408=) rs199584370 0.00035
NM_001130823.3(DNMT1):c.393C>T (p.Pro131=) rs143904813 0.00024
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys) rs138841970 0.00024
NM_001130823.3(DNMT1):c.387C>T (p.Pro129=) rs369470867 0.00019
NM_001130823.3(DNMT1):c.4146G>A (p.Thr1382=) rs184125970 0.00017
NM_001130823.3(DNMT1):c.633A>G (p.Glu211=) rs141264613 0.00017
NM_001130823.3(DNMT1):c.1896G>A (p.Thr632=) rs202058239 0.00016
NM_001130823.3(DNMT1):c.2475G>A (p.Ser825=) rs368834599 0.00016
NM_001130823.3(DNMT1):c.301C>T (p.Arg101Trp) rs369196079 0.00014
NM_001130823.3(DNMT1):c.2667C>T (p.Tyr889=) rs199832007 0.00013
NM_001130823.3(DNMT1):c.1320C>T (p.Thr440=) rs143925123 0.00011
NM_001130823.3(DNMT1):c.3576G>A (p.Ala1192=) rs772752543 0.00011
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044 0.00011
NM_001130823.3(DNMT1):c.3711C>T (p.Cys1237=) rs139909192 0.00010
NM_001130823.3(DNMT1):c.1749C>T (p.Ala583=) rs569985466 0.00009
NM_001130823.3(DNMT1):c.3523+6C>T rs372240993 0.00009
NM_001130823.3(DNMT1):c.390A>G (p.Lys130=) rs373499917 0.00009
NM_001130823.3(DNMT1):c.4032G>A (p.Pro1344=) rs150774582 0.00009
NM_001130823.3(DNMT1):c.483T>C (p.Thr161=) rs764496230 0.00009
NM_001130823.3(DNMT1):c.1722G>A (p.Val574=) rs140376680 0.00006
NM_001130823.3(DNMT1):c.1861A>C (p.Arg621=) rs144567470 0.00006
NM_001130823.3(DNMT1):c.2625C>T (p.Asp875=) rs200928585 0.00006
NM_001130823.3(DNMT1):c.3669C>T (p.Arg1223=) rs147755768 0.00006
NM_001130823.3(DNMT1):c.4894G>C (p.Asp1632His) rs147118268 0.00005
NM_001130823.3(DNMT1):c.4173G>A (p.Pro1391=) rs550868730 0.00004
NM_001130823.3(DNMT1):c.1911C>T (p.Thr637=) rs745677290 0.00003
NM_001130823.3(DNMT1):c.1149T>C (p.Tyr383=) rs766807027 0.00002
NM_001130823.3(DNMT1):c.2622C>T (p.Asp874=) rs375136816 0.00002
NM_001130823.3(DNMT1):c.2835C>T (p.Asn945=) rs539948794 0.00002
NM_001130823.3(DNMT1):c.1167C>T (p.Asp389=) rs140747287 0.00001
NM_001130823.3(DNMT1):c.1743C>T (p.Asp581=) rs751873043 0.00001
NM_001130823.3(DNMT1):c.2019+8C>A rs767465634 0.00001
NM_001130823.3(DNMT1):c.3163A>G (p.Ile1055Val) rs754199607 0.00001
NM_001130823.3(DNMT1):c.2088A>G (p.Gly696=)
NM_001130823.3(DNMT1):c.2289T>C (p.Tyr763=)
NM_001130823.3(DNMT1):c.2697G>A (p.Gln899=) rs530293931
NM_001130823.3(DNMT1):c.2922C>T (p.Arg974=)
NM_001130823.3(DNMT1):c.3759G>A (p.Ser1253=)
NM_001130823.3(DNMT1):c.3909G>A (p.Leu1303=) rs758806907
NM_001130823.3(DNMT1):c.4881G>A (p.Glu1627=)
NM_001130823.3(DNMT1):c.735G>A (p.Thr245=)

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