ClinVar Miner

List of variants reported as likely benign for Epilepsy, lateral temporal lobe, autosomal dominant

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Total variants: 13
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NM_001308275.1(LGI1):c.-280G>C rs74150339
NM_005097.4(LGI1):c.*215T>C rs17502662
NM_005097.4(LGI1):c.1026C>G (p.Asn342Lys) rs1554907730
NM_005097.4(LGI1):c.1155A>C (p.Leu385=) rs202148793
NM_005097.4(LGI1):c.1668C>T (p.Ser556=) rs763654125
NM_005097.4(LGI1):c.303C>T (p.Asn101=) rs762343857
NM_005097.4(LGI1):c.618C>T (p.Tyr206=) rs1554907108
NM_005097.4(LGI1):c.657= (p.Phe219=) rs1111820
NM_005097.4(LGI1):c.674-5dup rs1467827240
NM_005097.4(LGI1):c.717A>C (p.Ile239=) rs146425212
NM_005097.4(LGI1):c.738T>A (p.Asn246Lys) rs781404129
NM_005097.4(LGI1):c.838+10G>A rs756267808
NM_005097.4(LGI1):c.882G>A (p.Gln294=) rs1554907709

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