ClinVar Miner

List of variants in gene DNM1 studied for Lennox-Gastaut syndrome

Included ClinVar conditions (6):
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Gene type:
ClinVar version:
Total variants: 115
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HGVS dbSNP
NC_000009.12:g.(?_128234001)_(128234127_?)del
NM_004408.4(DNM1):c.1036G>A (p.Gly346Ser) rs1554774575
NM_004408.4(DNM1):c.1075G>A (p.Gly359Arg) rs1554774587
NM_004408.4(DNM1):c.1076G>C (p.Gly359Ala) rs587777862
NM_004408.4(DNM1):c.1081C>G (p.Arg361Gly)
NM_004408.4(DNM1):c.1090_1091insTTCCAC (p.Arg364_Ile365insLeuPro) rs1564332930
NM_004408.4(DNM1):c.1098C>T (p.Phe366=)
NM_004408.4(DNM1):c.1146G>A (p.Lys382=)
NM_004408.4(DNM1):c.1161G>A (p.Glu387=) rs998519750
NM_004408.4(DNM1):c.1176C>T (p.Ile392=)
NM_004408.4(DNM1):c.1196+4C>T
NM_004408.4(DNM1):c.1196+5G>A
NM_004408.4(DNM1):c.1196+8T>C
NM_004408.4(DNM1):c.1197-6G>A rs767877912
NM_004408.4(DNM1):c.1197-7C>T rs41306488
NM_004408.4(DNM1):c.1200G>A (p.Thr400=) rs373198034
NM_004408.4(DNM1):c.1246C>G (p.Gln416Glu)
NM_004408.4(DNM1):c.1261C>T (p.Arg421Ter) rs200535620
NM_004408.4(DNM1):c.1315G>A (p.Val439Ile)
NM_004408.4(DNM1):c.1335+8G>A rs374438127
NM_004408.4(DNM1):c.1336-7T>C
NM_004408.4(DNM1):c.1350G>T (p.Pro450=) rs147897973
NM_004408.4(DNM1):c.1358G>A (p.Arg453Gln) rs750296552
NM_004408.4(DNM1):c.1386C>T (p.Thr462=) rs372666180
NM_004408.4(DNM1):c.1390A>G (p.Ile464Val) rs992608425
NM_004408.4(DNM1):c.1401C>T (p.Arg467=)
NM_004408.4(DNM1):c.1409G>A (p.Arg470His) rs763830358
NM_004408.4(DNM1):c.1422+6C>T
NM_004408.4(DNM1):c.1422+7C>A rs761674210
NM_004408.4(DNM1):c.1423-8C>A rs555786484
NM_004408.4(DNM1):c.1437C>T (p.Ile479=) rs141788807
NM_004408.4(DNM1):c.1443C>T (p.Ile481=) rs778321233
NM_004408.4(DNM1):c.1493+14del rs371426966
NM_004408.4(DNM1):c.1558-3C>T rs546517702
NM_004408.4(DNM1):c.1568A>G (p.Lys523Arg)
NM_004408.4(DNM1):c.1586A>G (p.Asn529Ser) rs150040014
NM_004408.4(DNM1):c.1615A>G (p.Lys539Glu) rs1554781553
NM_004408.4(DNM1):c.1662G>A (p.Lys554=)
NM_004408.4(DNM1):c.1707C>T (p.Asn569=) rs145318071
NM_004408.4(DNM1):c.1764C>T (p.Leu588=) rs111534551
NM_004408.4(DNM1):c.1772C>T (p.Thr591Met) rs772239774
NM_004408.4(DNM1):c.1782-9A>G rs201739236
NM_004408.4(DNM1):c.1786G>A (p.Val596Ile)
NM_004408.4(DNM1):c.1810G>A (p.Glu604Lys)
NM_004408.4(DNM1):c.1850A>G (p.Lys617Arg) rs1564352065
NM_004408.4(DNM1):c.1872C>T (p.Gly624=) rs1367619284
NM_004408.4(DNM1):c.1889T>C (p.Val630Ala)
NM_004408.4(DNM1):c.1891G>C (p.Gly631Arg)
NM_004408.4(DNM1):c.1893+9C>A rs769121301
NM_004408.4(DNM1):c.1906-6T>C rs138961089
NM_004408.4(DNM1):c.1932C>T (p.Ser644=)
NM_004408.4(DNM1):c.1933G>A (p.Asp645Asn)
NM_004408.4(DNM1):c.2009T>C (p.Met670Thr) rs1437208936
NM_004408.4(DNM1):c.2028C>G (p.Thr676=) rs1339784958
NM_004408.4(DNM1):c.2076+4C>T rs374379668
NM_004408.4(DNM1):c.2133G>A (p.Gln711=)
NM_004408.4(DNM1):c.2156C>G (p.Ala719Gly)
NM_004408.4(DNM1):c.2159A>G (p.Glu720Gly)
NM_004408.4(DNM1):c.216G>A (p.Gln72=)
NM_004408.4(DNM1):c.2171G>A (p.Arg724Gln)
NM_004408.4(DNM1):c.2187G>A (p.Leu729=)
NM_004408.4(DNM1):c.224A>G (p.Asn75Ser) rs551214260
NM_004408.4(DNM1):c.2253C>G (p.Ser751Arg)
NM_004408.4(DNM1):c.2318+10C>T
NM_004408.4(DNM1):c.2322G>T (p.Ser774=) rs566718787
NM_004408.4(DNM1):c.235+8C>T rs370555560
NM_004408.4(DNM1):c.2360C>T (p.Ala787Val) rs1363606775
NM_004408.4(DNM1):c.2361C>T (p.Ala787=) rs1041513039
NM_004408.4(DNM1):c.2364G>A (p.Val788=) rs904300233
NM_004408.4(DNM1):c.2418G>T (p.Gly806=) rs1413872976
NM_004408.4(DNM1):c.2420C>G (p.Ser807Cys) rs935756107
NM_004408.4(DNM1):c.2427G>T (p.Leu809=) rs897409469
NM_004408.4(DNM1):c.2429G>T (p.Gly810Val)
NM_004408.4(DNM1):c.2430G>A (p.Gly810=) rs1007155416
NM_004408.4(DNM1):c.2474C>T (p.Pro825Leu)
NM_004408.4(DNM1):c.2483C>T (p.Pro828Leu)
NM_004408.4(DNM1):c.2534G>A (p.Ser845Asn)
NM_004408.4(DNM1):c.2540C>T (p.Ser847Leu) rs199498658
NM_004408.4(DNM1):c.2541G>A (p.Ser847=) rs545142847
NM_004408.4(DNM1):c.332C>G (p.Thr111Ser) rs192913494
NM_004408.4(DNM1):c.357T>C (p.Pro119=) rs77325628
NM_004408.4(DNM1):c.383A>G (p.His128Arg) rs368475266
NM_004408.4(DNM1):c.402G>A (p.Leu134=)
NM_004408.4(DNM1):c.411G>T (p.Leu137=)
NM_004408.4(DNM1):c.414C>T (p.Pro138=) rs141748215
NM_004408.4(DNM1):c.431C>T (p.Pro144Leu)
NM_004408.4(DNM1):c.442C>A (p.Gln148Lys) rs1554772945
NM_004408.4(DNM1):c.443A>G (p.Gln148Arg) rs1554772959
NM_004408.4(DNM1):c.450C>G (p.Pro150=) rs143834670
NM_004408.4(DNM1):c.465_467dup (p.Ile156_Arg157insMet) rs1057518655
NM_004408.4(DNM1):c.529G>C (p.Ala177Pro) rs587777860
NM_004408.4(DNM1):c.588G>A (p.Gln196=)
NM_004408.4(DNM1):c.599C>T (p.Thr200Ile)
NM_004408.4(DNM1):c.604G>A (p.Gly202Arg) rs1057524561
NM_004408.4(DNM1):c.618G>C (p.Lys206Asn) rs587777861
NM_004408.4(DNM1):c.624C>T (p.Asp208=) rs1395270062
NM_004408.4(DNM1):c.643_646delinsA (p.Asp215_Ala216delinsThr)
NM_004408.4(DNM1):c.695T>C (p.Ile232Thr)
NM_004408.4(DNM1):c.709C>T (p.Arg237Trp) rs760270633
NM_004408.4(DNM1):c.747C>T (p.Thr249=) rs141651183
NM_004408.4(DNM1):c.766C>T (p.Arg256Ter)
NM_004408.4(DNM1):c.775T>C (p.Phe259Leu)
NM_004408.4(DNM1):c.796C>T (p.Arg266Cys)
NM_004408.4(DNM1):c.797G>A (p.Arg266His) rs200136679
NM_004408.4(DNM1):c.804G>A (p.Leu268=)
NM_004408.4(DNM1):c.824C>T (p.Pro275Leu)
NM_004408.4(DNM1):c.825C>G (p.Pro275=)
NM_004408.4(DNM1):c.849+6C>T rs527412689
NM_004408.4(DNM1):c.850C>T (p.Gln284Ter)
NM_004408.4(DNM1):c.853C>T (p.Leu285=)
NM_004408.4(DNM1):c.865A>T (p.Ile289Phe) rs1554774401
NM_004408.4(DNM1):c.882G>A (p.Pro294=) rs559572430
NM_004408.4(DNM1):c.905G>A (p.Ser302Asn) rs1564332436
NM_004408.4(DNM1):c.920T>C (p.Ile307Thr) rs1052613908
NM_004408.4(DNM1):c.985C>G (p.Leu329Val)

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