ClinVar Miner

List of variants in gene DNM1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_004408.4(DNM1):c.1782-186G>A rs117907146 0.02699
NM_004408.4(DNM1):c.2535-91G>A rs116177116 0.01074
NM_004408.4(DNM1):c.2077-256_2077-255del rs148263791 0.01030
NM_004408.4(DNM1):c.2077-279_2077-278insG rs558248028 0.01016
NM_004408.4(DNM1):c.1906-156A>G rs114207651 0.01010
NM_004408.4(DNM1):c.1905+222C>T rs145755265 0.00974
NM_004408.4(DNM1):c.1558-272G>T rs146849993 0.00835
NM_004408.4(DNM1):c.1672-269G>A rs529729927 0.00729
NM_004408.4(DNM1):c.1197-182C>A rs150630047 0.00590
NM_004408.4(DNM1):c.1557+267T>C rs117869212 0.00588
NM_004408.4(DNM1):c.1197-330C>T rs182297664 0.00586
NM_004408.4(DNM1):c.1781+66G>C rs115492588 0.00574
NM_004408.4(DNM1):c.2535-117C>T rs140400419 0.00481
NM_004408.4(DNM1):c.1423-155G>A rs565923078 0.00445
NM_004408.4(DNM1):c.2076+107G>A rs7874719 0.00394
NM_004408.4(DNM1):c.850-23C>G rs182060568 0.00345
NM_004408.4(DNM1):c.849+95T>G rs139408895 0.00199
NM_004408.4(DNM1):c.1893+209G>C rs185477747 0.00135
NM_004408.4(DNM1):c.1782-9A>G rs201739236 0.00090
NM_004408.4(DNM1):c.1437C>T (p.Ile479=) rs141788807 0.00036
NM_004408.4(DNM1):c.1335+1634C>T rs377716564 0.00034
NM_004408.4(DNM1):c.1386C>T (p.Thr462=) rs372666180 0.00020
NM_004408.4(DNM1):c.1586A>G (p.Asn529Ser) rs150040014 0.00019
NM_004408.4(DNM1):c.1335+8G>A rs374438127 0.00016
NM_004408.4(DNM1):c.1315G>A (p.Val439Ile) rs771062230 0.00009
NM_004408.4(DNM1):c.1772C>T (p.Thr591Met) rs772239774 0.00007
NM_004408.4(DNM1):c.1350G>T (p.Pro450=) rs147897973 0.00006
NM_004408.4(DNM1):c.992+13C>A rs762733307 0.00006
NM_004408.4(DNM1):c.1422+7C>A rs761674210 0.00005
NM_004408.4(DNM1):c.1893+12G>A rs376700785 0.00005
NM_004408.4(DNM1):c.1493+16G>C rs746358072 0.00004
NM_004408.4(DNM1):c.2238C>T (p.Asn746=) rs1057521629 0.00004
NM_004408.4(DNM1):c.850-18C>T rs763158060 0.00004
NM_004408.4(DNM1):c.1176C>T (p.Ile392=) rs760314213 0.00003
NM_004408.4(DNM1):c.1335+16G>A rs768442528 0.00003
NM_004408.4(DNM1):c.1893+9C>A rs769121301 0.00003
NM_004408.4(DNM1):c.1197-15G>A rs534677463 0.00002
NM_004408.4(DNM1):c.1423-14A>G rs765225886 0.00002
NM_004408.4(DNM1):c.1558-17G>T rs749222845 0.00002
NM_004408.4(DNM1):c.1755C>T (p.Ile585=) rs759079310 0.00002
NM_004408.4(DNM1):c.1933G>A (p.Asp645Asn) rs754501788 0.00002
NM_004408.4(DNM1):c.850-17C>G rs764505046 0.00002
NM_004408.4(DNM1):c.1053C>T (p.Ile351=) rs1420306273 0.00001
NM_004408.4(DNM1):c.1196+14C>T rs372024347 0.00001
NM_004408.4(DNM1):c.1422+3G>A rs1280163668 0.00001
NM_004408.4(DNM1):c.1524G>A (p.Lys508=) rs1057523085 0.00001
NM_004408.4(DNM1):c.1558-14C>T rs971301728 0.00001
NM_004408.4(DNM1):c.1558-3C>T rs546517702 0.00001
NM_004408.4(DNM1):c.1743G>A (p.Ser581=) rs776254391 0.00001
NM_004408.4(DNM1):c.1906-6T>C rs138961089 0.00001
NM_004408.4(DNM1):c.2178C>A (p.Asp726Glu) rs745835138 0.00001
NM_004408.4(DNM1):c.2536C>T (p.Arg846Ter) rs752575279 0.00001
NM_004408.4(DNM1):c.633C>T (p.Asp211=) rs1043525791 0.00001
NM_004408.4(DNM1):c.822G>A (p.Thr274=) rs765410948 0.00001
NM_004408.4(DNM1):c.*19C>T rs1057523362
NM_004408.4(DNM1):c.1005G>A (p.Gln335=) rs1554774560
NM_004408.4(DNM1):c.1129-14G>A rs1588370648
NM_004408.4(DNM1):c.1335+93G>T rs115750361
NM_004408.4(DNM1):c.1371G>T (p.Glu457Asp) rs1835858946
NM_004408.4(DNM1):c.1422+9C>G rs760832551
NM_004408.4(DNM1):c.1557+16G>A rs1554780910
NM_004408.4(DNM1):c.1558-20_1558-18del rs1193085933
NM_004408.4(DNM1):c.1672-148C>G rs186892072
NM_004408.4(DNM1):c.1893+16A>C rs774161718
NM_004408.4(DNM1):c.1905+133C>G rs112610495
NM_004408.4(DNM1):c.1920G>A (p.Glu640=) rs1554784647
NM_004408.4(DNM1):c.1987C>A (p.Arg663=) rs777360250
NM_004408.4(DNM1):c.2391C>T (p.Gly797=) rs1057521943
NM_004408.4(DNM1):c.612C>T (p.Ile204=) rs1057523005

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