ClinVar Miner

List of variants studied for Epilepsy, lateral temporal lobe, autosomal dominant by Illumina Clinical Services Laboratory,Illumina

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Total variants: 17
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HGVS dbSNP
NM_001308275.1(LGI1):c.-227T>C rs150194814
NM_001308275.1(LGI1):c.-280G>C rs74150339
NM_001308275.1(LGI1):c.-304C>T rs886047484
NM_005097.4(LGI1):c.*215T>C rs17502662
NM_005097.4(LGI1):c.*323A>C rs767119123
NM_005097.4(LGI1):c.*338G>C rs182654305
NM_005097.4(LGI1):c.*59T>A rs886047488
NM_005097.4(LGI1):c.-168G>A rs879390887
NM_005097.4(LGI1):c.-66G>C rs886047485
NM_005097.4(LGI1):c.1125G>C (p.Ala375=) rs886047487
NM_005097.4(LGI1):c.1155A>C (p.Leu385=) rs202148793
NM_005097.4(LGI1):c.1336A>C (p.Ile446Leu) rs769204967
NM_005097.4(LGI1):c.135G>C (p.Val45=) rs768003944
NM_005097.4(LGI1):c.1392G>A (p.Ser464=) rs148804268
NM_005097.4(LGI1):c.345A>G (p.Pro115=) rs151104648
NM_005097.4(LGI1):c.818G>A (p.Arg273Gln) rs750249658
NM_005097.4(LGI1):c.838+11C>T rs886047486

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