ClinVar Miner

List of variants in gene DNMT1 reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_001130823.3(DNMT1):c.1287C>T (p.Tyr429=) rs536069799
NM_001130823.3(DNMT1):c.1314C>T (p.Ile438=)
NM_001130823.3(DNMT1):c.150C>T (p.His50=) rs146112081
NM_001130823.3(DNMT1):c.2387C>T (p.Thr796Met) rs148987580
NM_001130823.3(DNMT1):c.2472G>A (p.Thr824=) rs45484792
NM_001130823.3(DNMT1):c.2676C>T (p.Phe892=) rs139861062
NM_001130823.3(DNMT1):c.2721-10T>A rs377355204
NM_001130823.3(DNMT1):c.2728G>T (p.Val910Leu) rs150863675
NM_001130823.3(DNMT1):c.2835C>T (p.Asn945=) rs539948794
NM_001130823.3(DNMT1):c.290A>G (p.His97Arg) rs16999593
NM_001130823.3(DNMT1):c.2937C>T (p.Pro979=)
NM_001130823.3(DNMT1):c.2950C>A (p.Leu984Met)
NM_001130823.3(DNMT1):c.3156C>T (p.His1052=) rs141856197
NM_001130823.3(DNMT1):c.3196G>A (p.Val1066Met) rs187394074
NM_001130823.3(DNMT1):c.3224G>A (p.Arg1075His) rs779489678
NM_001130823.3(DNMT1):c.327C>T (p.Asn109=)
NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys) rs201308454
NM_001130823.3(DNMT1):c.3523+9C>T rs886043812
NM_001130823.3(DNMT1):c.3806+6C>T rs371779379
NM_001130823.3(DNMT1):c.3949-5C>G rs773047717
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met) rs377146699
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln) rs142647321
NM_001130823.3(DNMT1):c.4554C>T (p.His1518=) rs753248212
NM_001130823.3(DNMT1):c.469G>A (p.Ala157Thr) rs886044275
NM_001130823.3(DNMT1):c.614C>T (p.Ser205Leu)
NM_001130823.3(DNMT1):c.734C>T (p.Thr245Met) rs143598088
NM_001130823.3(DNMT1):c.891+8C>T rs117294281
NM_001130823.3(DNMT1):c.926+10T>G rs886044170
NM_001130823.3(DNMT1):c.979A>G (p.Ile327Val) rs2228612

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