ClinVar Miner

List of variants in gene DNMT1 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP
NM_001130823.3(DNMT1):c.1044-9T>C rs533403196
NM_001130823.3(DNMT1):c.1053A>G (p.Lys351=) rs139355567
NM_001130823.3(DNMT1):c.1320C>T (p.Thr440=) rs143925123
NM_001130823.3(DNMT1):c.1608C>T (p.Ser536=) rs553962731
NM_001130823.3(DNMT1):c.1821G>A (p.Thr607=) rs371848582
NM_001130823.3(DNMT1):c.1833-4G>A rs753887750
NM_001130823.3(DNMT1):c.1861A>C (p.Arg621=) rs144567470
NM_001130823.3(DNMT1):c.1896G>A (p.Thr632=) rs202058239
NM_001130823.3(DNMT1):c.1911C>T (p.Thr637=) rs745677290
NM_001130823.3(DNMT1):c.1986C>T (p.Asn662=) rs377704053
NM_001130823.3(DNMT1):c.2020-10C>T rs369373339
NM_001130823.3(DNMT1):c.2268T>C (p.Thr756=) rs374841430
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792
NM_001130823.3(DNMT1):c.2475G>A (p.Ser825=) rs368834599
NM_001130823.3(DNMT1):c.2625C>T (p.Asp875=) rs200928585
NM_001130823.3(DNMT1):c.2667C>T (p.Tyr889=) rs199832007
NM_001130823.3(DNMT1):c.2979C>T (p.Ser993=) rs771269343
NM_001130823.3(DNMT1):c.3117-9C>T rs199546819
NM_001130823.3(DNMT1):c.3156C>T (p.His1052=) rs141856197
NM_001130823.3(DNMT1):c.3806+6C>T rs371779379
NM_001130823.3(DNMT1):c.3831G>T (p.Arg1277=) rs1405376714
NM_001130823.3(DNMT1):c.3840C>G (p.Leu1280=) rs1436599621
NM_001130823.3(DNMT1):c.387C>T (p.Pro129=) rs369470867
NM_001130823.3(DNMT1):c.390A>G (p.Lys130=) rs373499917
NM_001130823.3(DNMT1):c.3936C>T (p.Phe1312=) rs367637414
NM_001130823.3(DNMT1):c.393C>T (p.Pro131=) rs143904813
NM_001130823.3(DNMT1):c.3975T>C (p.Thr1325=) rs768712864
NM_001130823.3(DNMT1):c.4140C>T (p.Thr1380=) rs749741623
NM_001130823.3(DNMT1):c.4146G>A (p.Thr1382=) rs184125970
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.3(DNMT1):c.483T>C (p.Thr161=) rs764496230
NM_001130823.3(DNMT1):c.493+1G>A rs975957081
NM_001130823.3(DNMT1):c.493+7G>A rs1177224966
NM_001130823.3(DNMT1):c.493+8C>T rs138998574
NM_001130823.3(DNMT1):c.520A>C (p.Thr174Pro) rs201319352
NM_001130823.3(DNMT1):c.569+10C>T rs781605215
NM_001130823.3(DNMT1):c.687T>G (p.Val229=) rs61758429
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu) rs150999369
NM_001130823.3(DNMT1):c.981T>G (p.Ile327Met) rs61758431

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