ClinVar Miner

List of variants reported as not provided for Generalized epilepsy with febrile seizures plus, type 1

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Total variants: 23
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HGVS dbSNP
NM_006920.6(SCN1A):c.1130G>A (p.Arg377Gln) rs121917957
NM_006920.6(SCN1A):c.1162T>C (p.Tyr388His) rs121918781
NM_006920.6(SCN1A):c.220T>C (p.Ser74Pro) rs121917931
NM_006920.6(SCN1A):c.2336A>G (p.Tyr779Cys) rs121918782
NM_006920.6(SCN1A):c.2542C>T (p.Arg848Cys) rs121918784
NM_006920.6(SCN1A):c.2591C>T (p.Thr864Met) rs121918623
NM_006920.6(SCN1A):c.3577T>C (p.Trp1193Arg) rs121917930
NM_006920.6(SCN1A):c.3776A>C (p.Lys1259Thr) rs121918626
NM_006920.6(SCN1A):c.3892C>T (p.Leu1298Phe) rs121918801
NM_006920.6(SCN1A):c.4024G>C (p.Val1342Leu) rs121917954
NM_006920.6(SCN1A):c.4063G>A (p.Val1355Ile) rs121918805
NM_006920.6(SCN1A):c.4250T>C (p.Val1417Ala) rs121918627
NM_006920.6(SCN1A):c.4935C>G (p.Ile1645Met) rs121917955
NM_006920.6(SCN1A):c.4936C>T (p.Arg1646Cys) rs121918811
NM_006920.6(SCN1A):c.5021C>T (p.Ala1674Val) rs121918744
NM_006920.6(SCN1A):c.5027T>C (p.Phe1676Ser) rs121917932
NM_006920.6(SCN1A):c.5192A>G (p.Asp1731Gly) rs121918812
NM_006920.6(SCN1A):c.5350G>A (p.Glu1784Lys) rs121918813
NM_006920.6(SCN1A):c.5522T>C (p.Met1841Thr) rs121918783
NM_006920.6(SCN1A):c.5536G>T (p.Val1846Leu) rs121918814
NM_006920.6(SCN1A):c.5563G>T (p.Asp1855Tyr) rs121918815
NM_006920.6(SCN1A):c.563A>T (p.Asp188Val) rs121917953
NM_006920.6(SCN1A):c.80G>C (p.Arg27Thr) rs121917906

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