ClinVar Miner

List of variants in gene DNMT1 reported by Eurofins NTD LLC (GA)

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001130823.3(DNMT1):c.979A>G (p.Ile327Val) rs2228612 0.10575
NM_001130823.3(DNMT1):c.290A>G (p.His97Arg) rs16999593 0.00959
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.2676C>T (p.Phe892=) rs139861062 0.00108
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792 0.00067
NM_001130823.3(DNMT1):c.1287C>T (p.Tyr429=) rs536069799 0.00010
NM_001130823.3(DNMT1):c.2721-10T>A rs377355204 0.00010
NM_001130823.3(DNMT1):c.2728G>T (p.Val910Leu) rs150863675 0.00010
NM_001130823.3(DNMT1):c.2937C>T (p.Pro979=) rs150359172 0.00008
NM_001130823.3(DNMT1):c.327C>T (p.Asn109=) rs144685297 0.00007
NM_001130823.3(DNMT1):c.734C>T (p.Thr245Met) rs143598088 0.00007
NM_001130823.3(DNMT1):c.1314C>T (p.Ile438=) rs201487376 0.00006
NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys) rs201308454 0.00006
NM_001130823.3(DNMT1):c.3806+6C>T rs371779379 0.00006
NM_001130823.3(DNMT1):c.2387C>T (p.Thr796Met) rs148987580 0.00005
NM_001130823.3(DNMT1):c.3156C>T (p.His1052=) rs141856197 0.00004
NM_001130823.3(DNMT1):c.3196G>A (p.Val1066Met) rs187394074 0.00004
NM_001130823.3(DNMT1):c.2835C>T (p.Asn945=) rs539948794 0.00002
NM_001130823.3(DNMT1):c.2950C>A (p.Leu984Met) rs760683699 0.00002
NM_001130823.3(DNMT1):c.3224G>A (p.Arg1075His) rs779489678 0.00001
NM_001130823.3(DNMT1):c.614C>T (p.Ser205Leu) rs781646588 0.00001
NM_001130823.3(DNMT1):c.926+10T>G rs886044170 0.00001
NM_001130823.3(DNMT1):c.3523+9C>T rs886043812
NM_001130823.3(DNMT1):c.3949-5C>G rs773047717
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699
NM_001130823.3(DNMT1):c.469G>A (p.Ala157Thr) rs886044275

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.