ClinVar Miner

List of variants in gene DNM2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001005361.3(DNM2):c.236-29C>G rs3826803 0.56569
NM_001005361.3(DNM2):c.2139T>C (p.Ala713=) rs2229920 0.30148
NM_001005361.3(DNM2):c.1545+41C>T rs2287029 0.12846
NM_001005361.3(DNM2):c.1077C>T (p.Gly359=) rs112238216 0.02416
NM_001005361.3(DNM2):c.2484G>A (p.Pro828=) rs114682382 0.01064
NM_001005361.3(DNM2):c.235+12C>A rs147026993 0.00953
NM_001005361.3(DNM2):c.235+6A>G rs113192269 0.00748
NM_001005361.3(DNM2):c.1129-40C>T rs199742926 0.00375
NM_001005361.3(DNM2):c.2543+7C>G rs201979143 0.00364
NM_001005361.3(DNM2):c.236-8C>G rs143084059 0.00361
NM_001005361.3(DNM2):c.519T>C (p.Ala173=) rs77702567 0.00359
NM_001005361.3(DNM2):c.1545+14C>G rs114713494 0.00350
NM_001005361.3(DNM2):c.643G>A (p.Asp215Asn) rs145478270 0.00168
NM_001005361.3(DNM2):c.2160C>T (p.Asp720=) rs117598326 0.00163
NM_001005361.3(DNM2):c.238C>T (p.His80Tyr) rs148790687 0.00123
NM_001005361.3(DNM2):c.645C>T (p.Asp215=) rs148900299 0.00028
NM_001005361.3(DNM2):c.2511G>A (p.Arg837=) rs200100669 0.00027
NM_001005361.3(DNM2):c.882G>A (p.Pro294=) rs144790170 0.00018
NM_001005361.3(DNM2):c.480C>T (p.Ile160=) rs140036663 0.00017
NM_001005361.3(DNM2):c.528C>T (p.Pro176=) rs147579870 0.00015
NM_001005361.3(DNM2):c.789G>A (p.Pro263=) rs199976453 0.00014
NM_001005361.3(DNM2):c.822G>A (p.Thr274=) rs201763720 0.00014
NM_001005361.3(DNM2):c.1827C>T (p.Ser609=) rs371412466 0.00013
NM_001005361.3(DNM2):c.2313G>A (p.Pro771=) rs147463138 0.00009
NM_001005361.3(DNM2):c.1196+652C>T rs377319162 0.00008
NM_001005361.3(DNM2):c.384C>T (p.His128=) rs201089328 0.00005
NM_001005361.3(DNM2):c.1731G>A (p.Lys577=) rs35365412 0.00002
NM_001005361.3(DNM2):c.1857G>A (p.Ser619=) rs377009386 0.00001
NM_001005361.3(DNM2):c.216G>A (p.Gln72=) rs368075301 0.00001
NM_001005361.3(DNM2):c.2391C>T (p.Pro797=) rs777834732 0.00001
NM_001005361.3(DNM2):c.243C>T (p.Ala81=) rs755366581 0.00001
NM_001005361.3(DNM2):c.1102G>A (p.Glu368Lys) rs121909092
NM_001005361.3(DNM2):c.162-9C>G rs200736669
NM_001005361.3(DNM2):c.1985C>T (p.Ser662Leu)
NM_001005361.3(DNM2):c.2328C>A (p.His776Gln) rs766387630
NM_001005361.3(DNM2):c.579C>G (p.Val193=)
NM_001005361.3(DNM2):c.590-31CCTCTGA[3] rs748362325
NM_001005361.3(DNM2):c.960C>A (p.Asp320Glu)

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