ClinVar Miner

List of variants in gene DNM1 reported as likely benign for Lennox-Gastaut syndrome

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_004408.4(DNM1):c.1098C>T (p.Phe366=) rs532535557
NM_004408.4(DNM1):c.1146G>A (p.Lys382=) rs150617335
NM_004408.4(DNM1):c.1161G>A (p.Glu387=) rs998519750
NM_004408.4(DNM1):c.1176C>T (p.Ile392=) rs760314213
NM_004408.4(DNM1):c.1196+8T>C rs1588370851
NM_004408.4(DNM1):c.1197-6G>A rs767877912
NM_004408.4(DNM1):c.1200G>A (p.Thr400=) rs373198034
NM_004408.4(DNM1):c.1335+8G>A rs374438127
NM_004408.4(DNM1):c.1336-7T>C rs550764968
NM_004408.4(DNM1):c.1350G>T (p.Pro450=) rs147897973
NM_004408.4(DNM1):c.1386C>T (p.Thr462=) rs372666180
NM_004408.4(DNM1):c.1409G>A (p.Arg470His) rs763830358
NM_004408.4(DNM1):c.1422+7C>A rs761674210
NM_004408.4(DNM1):c.1443C>T (p.Ile481=) rs778321233
NM_004408.4(DNM1):c.1586A>G (p.Asn529Ser) rs150040014
NM_004408.4(DNM1):c.1707C>T (p.Asn569=) rs145318071
NM_004408.4(DNM1):c.1772C>T (p.Thr591Met) rs772239774
NM_004408.4(DNM1):c.1893+9C>A rs769121301
NM_004408.4(DNM1):c.1932C>T (p.Ser644=) rs750934085
NM_004408.4(DNM1):c.2009T>C (p.Met670Thr) rs1437208936
NM_004408.4(DNM1):c.2133G>A (p.Gln711=) rs1277551348
NM_004408.4(DNM1):c.216G>A (p.Gln72=) rs781185286
NM_004408.4(DNM1):c.2187G>A (p.Leu729=) rs749382749
NM_004408.4(DNM1):c.2322G>T (p.Ser774=) rs566718787
NM_004408.4(DNM1):c.235+8C>T rs370555560
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.2427G>T (p.Leu809=) rs897409469
NM_004408.4(DNM1):c.2430G>A (p.Gly810=) rs1007155416
NM_004408.4(DNM1):c.411G>T (p.Leu137=) rs1051766292
NM_004408.4(DNM1):c.414C>T (p.Pro138=) rs141748215
NM_004408.4(DNM1):c.599C>T (p.Thr200Ile)
NM_004408.4(DNM1):c.624C>T (p.Asp208=) rs1395270062
NM_004408.4(DNM1):c.766C>T (p.Arg256Ter)
NM_004408.4(DNM1):c.797G>A (p.Arg266His) rs200136679
NM_004408.4(DNM1):c.853C>T (p.Leu285=) rs546034278
NM_004408.4(DNM1):c.920T>C (p.Ile307Thr) rs1052613908

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