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
Download table as spreadsheet
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.