ClinVar Miner

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

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Total variants: 48
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HGVS dbSNP
NM_001308275.1(LGI1):c.-227T>C rs150194814
NM_001308275.1(LGI1):c.-304C>T rs886047484
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.1040T>C (p.Val347Ala)
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.1210A>T (p.Ser404Cys) rs1564853070
NM_005097.4(LGI1):c.1220G>A (p.Arg407His) rs201376381
NM_005097.4(LGI1):c.1283A>G (p.Asn428Ser)
NM_005097.4(LGI1):c.1290G>A (p.Glu430=)
NM_005097.4(LGI1):c.1318G>A (p.Val440Met)
NM_005097.4(LGI1):c.1331T>A (p.Val444Glu)
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.1370T>C (p.Val457Ala) rs1554907821
NM_005097.4(LGI1):c.1392G>A (p.Ser464=) rs148804268
NM_005097.4(LGI1):c.1439_1442del (p.Gln480fs) rs1554907835
NM_005097.4(LGI1):c.143G>A (p.Cys48Tyr) rs1554901937
NM_005097.4(LGI1):c.1465del (p.Tyr489fs)
NM_005097.4(LGI1):c.1471A>G (p.Ile491Val)
NM_005097.4(LGI1):c.1597C>T (p.Arg533Cys)
NM_005097.4(LGI1):c.1652T>C (p.Val551Ala)
NM_005097.4(LGI1):c.1669G>A (p.Ala557Thr) rs370955995
NM_005097.4(LGI1):c.191C>T (p.Thr64Ile) rs373616721
NM_005097.4(LGI1):c.205G>A (p.Val69Ile)
NM_005097.4(LGI1):c.215+7C>T
NM_005097.4(LGI1):c.269C>T (p.Thr90Met) rs796052692
NM_005097.4(LGI1):c.272C>T (p.Pro91Leu) rs796052693
NM_005097.4(LGI1):c.299C>T (p.Ser100Leu) rs1263918669
NM_005097.4(LGI1):c.310G>A (p.Asp104Asn) rs145675377
NM_005097.4(LGI1):c.345A>G (p.Pro115=) rs151104648
NM_005097.4(LGI1):c.398A>G (p.His133Arg) rs376452111
NM_005097.4(LGI1):c.407G>A (p.Arg136Gln) rs767254591
NM_005097.4(LGI1):c.464C>T (p.Pro155Leu)
NM_005097.4(LGI1):c.46C>G (p.Leu16Val) rs777973395
NM_005097.4(LGI1):c.625C>T (p.Arg209Cys)
NM_005097.4(LGI1):c.626G>A (p.Arg209His)
NM_005097.4(LGI1):c.634A>G (p.Asn212Asp) rs757629755
NM_005097.4(LGI1):c.647C>T (p.Ser216Leu)
NM_005097.4(LGI1):c.812C>T (p.Thr271Ile) rs140752487
NM_005097.4(LGI1):c.818G>A (p.Arg273Gln) rs750249658
NM_005097.4(LGI1):c.836C>G (p.Thr279Arg) rs1159639109
NM_005097.4(LGI1):c.837A>G (p.Thr279=) rs755068491
NM_005097.4(LGI1):c.838+11C>T rs886047486

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