ClinVar Miner

List of variants in gene DNM1 reported as uncertain significance for Lennox-Gastaut syndrome

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP
NC_000009.12:g.(?_128234001)_(128234127_?)del
NM_004408.4(DNM1):c.1196+5G>A
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.1358G>A (p.Arg453Gln) rs750296552
NM_004408.4(DNM1):c.1390A>G (p.Ile464Val) rs992608425
NM_004408.4(DNM1):c.1401C>T (p.Arg467=)
NM_004408.4(DNM1):c.1422+6C>T
NM_004408.4(DNM1):c.1568A>G (p.Lys523Arg)
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.1891G>C (p.Gly631Arg)
NM_004408.4(DNM1):c.2028C>G (p.Thr676=) rs1339784958
NM_004408.4(DNM1):c.2076+4C>T rs374379668
NM_004408.4(DNM1):c.2159A>G (p.Glu720Gly)
NM_004408.4(DNM1):c.2171G>A (p.Arg724Gln)
NM_004408.4(DNM1):c.224A>G (p.Asn75Ser) rs551214260
NM_004408.4(DNM1):c.2253C>G (p.Ser751Arg)
NM_004408.4(DNM1):c.2429G>T (p.Gly810Val)
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.383A>G (p.His128Arg) rs368475266
NM_004408.4(DNM1):c.402G>A (p.Leu134=)
NM_004408.4(DNM1):c.588G>A (p.Gln196=)
NM_004408.4(DNM1):c.604G>A (p.Gly202Arg) rs1057524561
NM_004408.4(DNM1):c.643_646delinsA (p.Asp215_Ala216delinsThr)
NM_004408.4(DNM1):c.695T>C (p.Ile232Thr)
NM_004408.4(DNM1):c.775T>C (p.Phe259Leu)
NM_004408.4(DNM1):c.796C>T (p.Arg266Cys)
NM_004408.4(DNM1):c.804G>A (p.Leu268=)
NM_004408.4(DNM1):c.824C>T (p.Pro275Leu)
NM_004408.4(DNM1):c.849+6C>T rs527412689
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.985C>G (p.Leu329Val)

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