ClinVar Miner

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

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 16
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HGVS dbSNP
NM_001130823.3(DNMT1):c.1066G>A (p.Ala356Thr) rs529074384
NM_001130823.3(DNMT1):c.1171-7C>T rs1168540279
NM_001130823.3(DNMT1):c.1314C>T (p.Ile438=) rs201487376
NM_001130823.3(DNMT1):c.150C>T (p.His50=) rs146112081
NM_001130823.3(DNMT1):c.2667C>T (p.Tyr889=) rs199832007
NM_001130823.3(DNMT1):c.2693C>T (p.Thr898Ile) rs201213597
NM_001130823.3(DNMT1):c.2835C>T (p.Asn945=) rs539948794
NM_001130823.3(DNMT1):c.3117-8G>A rs769623856
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys) rs138841970
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699
NM_001130823.3(DNMT1):c.4164C>T (p.Ser1388=)
NM_001130823.3(DNMT1):c.4173G>A (p.Pro1391=)
NM_001130823.3(DNMT1):c.483T>C (p.Thr161=) rs764496230
NM_001130823.3(DNMT1):c.694C>A (p.Pro232Thr) rs374856119
NM_001130823.3(DNMT1):c.867C>T (p.Asp289=) rs750916721
NM_001130823.3(DNMT1):c.977A>C (p.Gln326Pro) rs143287044

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