ClinVar Miner

Variants in gene DNMT1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 22
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HGVS dbSNP
NM_001130823.3(DNMT1):c.150C>T (p.His50=) rs146112081
NM_001130823.3(DNMT1):c.1896G>A (p.Thr632=) rs202058239
NM_001130823.3(DNMT1):c.2020-10C>T rs369373339
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792
NM_001130823.3(DNMT1):c.2626G>A (p.Gly876Arg) rs62621087
NM_001130823.3(DNMT1):c.2676C>T (p.Phe892=) rs139861062
NM_001130823.3(DNMT1):c.2693C>T (p.Thr898Ile) rs201213597
NM_001130823.3(DNMT1):c.3669C>T (p.Arg1223=) rs147755768
NM_001130823.3(DNMT1):c.387C>T (p.Pro129=) rs369470867
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.4146G>A (p.Thr1382=) rs184125970
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.3(DNMT1):c.4503C>T (p.Cys1501=) rs149271718
NM_001130823.3(DNMT1):c.4773+18C>T rs183300496
NM_001130823.3(DNMT1):c.4876G>A (p.Glu1626Lys) rs201774098
NM_001130823.3(DNMT1):c.493+8C>T rs138998574
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val) rs62621089
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu) rs150999369
NM_001130823.3(DNMT1):c.868G>A (p.Glu290Lys) rs200024502
NM_001130823.3(DNMT1):c.891+8C>T rs117294281
NM_001130823.3(DNMT1):c.981T>G (p.Ile327Met) rs61758431

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