ClinVar Miner

List of variants in gene DNM2 reported as likely benign for Charcot-Marie-Tooth disease, dominant intermediate B

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Total variants: 56
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HGVS dbSNP
NM_001005360.2(DNM2):c.1071C>T (p.Ser357=) rs779241319
NM_001005360.2(DNM2):c.1095C>A (p.Ile365=) rs746959606
NM_001005360.2(DNM2):c.1101C>T (p.His367=) rs768651920
NM_001005360.2(DNM2):c.1377C>T (p.Ile459=) rs369345296
NM_001005360.2(DNM2):c.1384A>G (p.Thr462Ala) rs201575500
NM_001005360.2(DNM2):c.1422+9C>T rs199952853
NM_001005360.2(DNM2):c.1437C>T (p.Ile479=) rs146506201
NM_001005360.2(DNM2):c.162-6del rs766449694
NM_001005360.2(DNM2):c.162-7C>T rs148318860
NM_001005360.2(DNM2):c.1773G>A (p.Thr591=) rs201604679
NM_001005360.2(DNM2):c.177C>T (p.Arg59=) rs762795230
NM_001005360.2(DNM2):c.1782-4G>A rs767424969
NM_001005360.2(DNM2):c.1782-4G>C rs767424969
NM_001005360.2(DNM2):c.1837G>A (p.Val613Met) rs748286191
NM_001005360.2(DNM2):c.2031G>A (p.Lys677=) rs768285660
NM_001005360.2(DNM2):c.2136G>T (p.Ser712=) rs1555716924
NM_001005360.2(DNM2):c.2179C>T (p.His727Tyr) rs142963320
NM_001005360.2(DNM2):c.2253T>C (p.Pro751=) rs200155565
NM_001005360.2(DNM2):c.2313G>A (p.Pro771=) rs147463138
NM_001005360.2(DNM2):c.238C>T (p.His80Tyr) rs148790687
NM_001005360.2(DNM2):c.2418G>A (p.Ala806=) rs200968756
NM_001005360.2(DNM2):c.2562G>A (p.Ala854=) rs761141093
NM_001005360.2(DNM2):c.2592C>T (p.Ala864=) rs373161548
NM_001005360.2(DNM2):c.316G>A (p.Asp106Asn) rs375151459
NM_001005360.2(DNM2):c.33G>A (p.Pro11=) rs779502758
NM_001005360.2(DNM2):c.384C>T (p.His128=) rs201089328
NM_001005360.2(DNM2):c.480C>T (p.Ile160=) rs140036663
NM_001005360.2(DNM2):c.528C>T (p.Pro176=) rs147579870
NM_001005360.2(DNM2):c.555C>T (p.Asp185=) rs140788791
NM_001005360.2(DNM2):c.633C>T (p.Asp211=) rs200191870
NM_001005360.2(DNM2):c.645C>T (p.Asp215=) rs148900299
NM_001005360.2(DNM2):c.750A>G (p.Ala250=) rs202214529
NM_001005360.2(DNM2):c.81C>T (p.Cys27=) rs534605878
NM_001005360.2(DNM2):c.822G>A (p.Thr274=) rs201763720
NM_001005360.2(DNM2):c.839C>T (p.Thr280Met) rs202155679
NM_001005360.2(DNM2):c.876G>A (p.Ser292=) rs749140605
NM_001005360.2(DNM2):c.882G>A (p.Pro294=) rs144790170
NM_001005360.2(DNM2):c.90C>T (p.Asp30=) rs759919549
NM_001005361.3(DNM2):c.1188T>C (p.His396=) rs1039592560
NM_001005361.3(DNM2):c.1196+625C>T rs542089703
NM_001005361.3(DNM2):c.1196+628G>C rs374376619
NM_001005361.3(DNM2):c.1196+652C>T rs377319162
NM_001005361.3(DNM2):c.1423-8T>C rs1599583116
NM_001005361.3(DNM2):c.1558-9T>G rs748026953
NM_001005361.3(DNM2):c.1608C>T (p.Gly536=) rs774973372
NM_001005361.3(DNM2):c.1965C>T (p.Thr655=) rs201972896
NM_001005361.3(DNM2):c.2312C>T (p.Pro771Leu) rs202060910
NM_001005361.3(DNM2):c.2514C>T (p.Ile838=) rs200782592
NM_001005361.3(DNM2):c.2607C>T (p.Leu869=) rs144472798
NM_001005361.3(DNM2):c.315C>T (p.Thr105=) rs111837150
NM_001005361.3(DNM2):c.453C>T (p.Asp151=) rs201681441
NM_001005361.3(DNM2):c.514C>T (p.Leu172=) rs1599530007
NM_001005361.3(DNM2):c.642C>G (p.Thr214=) rs752944817
NM_001005361.3(DNM2):c.807C>T (p.Ala269=) rs752361306
NM_001005361.3(DNM2):c.900A>G (p.Leu300=) rs1599552753
NM_001005361.3(DNM2):c.936G>A (p.Glu312=) rs949106319

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