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
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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

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