List of variants in gene LGI1 reported as likely benign for Epilepsy, lateral temporal lobe, autosomal dominant

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 13

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HGVS	dbSNP
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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