ClinVar Miner

List of variants in gene DNMT3B reported as likely benign for DNA repair disease

Included ClinVar conditions (97):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_006892.4(DNMT3B):c.*443C>T rs6058896
NM_006892.4(DNMT3B):c.1150G>A (p.Ala384Thr) rs150682895
NM_006892.4(DNMT3B):c.1211A>G (p.Tyr404Cys) rs143462810
NM_006892.4(DNMT3B):c.1218C>T (p.Asn406=) rs875040
NM_006892.4(DNMT3B):c.1359G>A (p.Gly453=) rs35216603
NM_006892.4(DNMT3B):c.1413C>T (p.Asp471=) rs6119965
NM_006892.4(DNMT3B):c.159G>A (p.Ser53=) rs145694804
NM_006892.4(DNMT3B):c.1760-8C>G rs2424926
NM_006892.4(DNMT3B):c.1878C>T (p.Asn626=) rs17123655
NM_006892.4(DNMT3B):c.1881C>T (p.Asp627=) rs17123657
NM_006892.4(DNMT3B):c.1996+6C>T rs77355896
NM_006892.4(DNMT3B):c.2097T>C (p.Val699=) rs369838649
NM_006892.4(DNMT3B):c.2142G>A (p.Leu714=) rs143847495
NM_006892.4(DNMT3B):c.273C>T (p.Phe91=) rs776835342
NM_006892.4(DNMT3B):c.608C>T (p.Pro203Leu) rs147945634
NM_006892.4(DNMT3B):c.654+9G>A rs1452971065
NM_006892.4(DNMT3B):c.732G>A (p.Val244=) rs201520258

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.