ClinVar Miner

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

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Total variants: 58
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HGVS dbSNP
NM_001005360.2(DNM2):c.*10G>A rs200188660
NM_001005360.2(DNM2):c.*14C>T rs369529119
NM_001005360.2(DNM2):c.*22C>T rs531170486
NM_001005360.2(DNM2):c.*268A>T rs12461992
NM_001005360.2(DNM2):c.*35C>G rs199700849
NM_001005360.2(DNM2):c.*385C>T rs78160240
NM_001005360.2(DNM2):c.*386G>C rs74952080
NM_001005360.2(DNM2):c.*453C>T rs200104482
NM_001005360.2(DNM2):c.*47G>A rs367938944
NM_001005360.2(DNM2):c.*601C>T rs185820576
NM_001005360.2(DNM2):c.*607G>A rs117954916
NM_001005360.2(DNM2):c.1077C>T (p.Gly359=) rs112238216
NM_001005360.2(DNM2):c.1218C>T (p.Asp406=) rs563985581
NM_001005360.2(DNM2):c.1286A>T (p.Asp429Val) rs186762327
NM_001005360.2(DNM2):c.1335+13C>T rs150975494
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.1423-12G>A rs376753915
NM_001005360.2(DNM2):c.1512G>A (p.Thr504=) rs767407905
NM_001005360.2(DNM2):c.162-7C>A rs148318860
NM_001005360.2(DNM2):c.1782-11C>T rs78580529
NM_001005360.2(DNM2):c.1782-5C>T rs200103145
NM_001005360.2(DNM2):c.1902C>T (p.Asn634=) rs2229919
NM_001005360.2(DNM2):c.190G>A (p.Val64Ile) rs144250390
NM_001005360.2(DNM2):c.2061G>A (p.Thr687=) rs149164657
NM_001005360.2(DNM2):c.2160C>T (p.Asp720=) rs117598326
NM_001005360.2(DNM2):c.2179C>T (p.His727Tyr) rs142963320
NM_001005360.2(DNM2):c.2201A>G (p.Asn734Ser) rs577767034
NM_001005360.2(DNM2):c.2313G>A (p.Pro771=) rs147463138
NM_001005360.2(DNM2):c.235+12C>A rs147026993
NM_001005360.2(DNM2):c.235+6A>G rs113192269
NM_001005360.2(DNM2):c.236-8C>G rs143084059
NM_001005360.2(DNM2):c.238C>T (p.His80Tyr) rs148790687
NM_001005360.2(DNM2):c.2484G>A (p.Pro828=) rs114682382
NM_001005360.2(DNM2):c.2511G>A (p.Arg837=) rs200100669
NM_001005360.2(DNM2):c.2543+7C>G rs201979143
NM_001005360.2(DNM2):c.2567G>A (p.Ser856Asn) rs149825590
NM_001005360.2(DNM2):c.386-6T>A rs114623441
NM_001005360.2(DNM2):c.450A>G (p.Pro150=) rs766121627
NM_001005360.2(DNM2):c.497G>A (p.Arg166Gln) rs200002469
NM_001005360.2(DNM2):c.519T>C (p.Ala173=) rs77702567
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.643G>A (p.Asp215Asn) rs145478270
NM_001005360.2(DNM2):c.666C>T (p.Asn222=) rs2229921
NM_001005360.2(DNM2):c.788C>T (p.Pro263Leu) rs3745674
NM_001005360.2(DNM2):c.789G>A (p.Pro263=) rs199976453
NM_001005360.2(DNM2):c.882G>A (p.Pro294=) rs144790170
NM_001005360.2(DNM2):c.890G>A (p.Arg297His) rs763894364
NM_001005360.2(DNM2):c.958G>A (p.Asp320Asn) rs150613209
NM_001005361.3(DNM2):c.*321A>G
NM_001005361.3(DNM2):c.*671T>C
NM_001005361.3(DNM2):c.1196+710G>A
NM_001005361.3(DNM2):c.1400G>A (p.Arg467Gln)
NM_001005361.3(DNM2):c.1558-7C>A rs184310103
NM_001005361.3(DNM2):c.1671+14G>A
NM_001005361.3(DNM2):c.2139T>C (p.Ala713=) rs2229920
NM_001005361.3(DNM2):c.386-6T>C rs114623441

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