ClinVar Miner

List of variants in gene LGI1 studied for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP
LGI1, 1-BP DEL, 835C
LGI1, 1320C-T
LGI1, 81-KB DEL
LGI1, IVS5DS, G-A, +1
NC_000010.11:g.(93704377_?)_(?_93785620)del
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.1013T>C (p.Phe338Ser) rs869025201
NM_005097.4(LGI1):c.1026C>G (p.Asn342Lys) rs1554907730
NM_005097.4(LGI1):c.1040T>C (p.Val347Ala)
NM_005097.4(LGI1):c.1125G>C (p.Ala375=) rs886047487
NM_005097.4(LGI1):c.1128G>A (p.Trp376Ter) rs1060502053
NM_005097.4(LGI1):c.1148A>C (p.Glu383Ala) rs28937874
NM_005097.4(LGI1):c.1155A>C (p.Leu385=) rs202148793
NM_005097.4(LGI1):c.1158_1168dup (p.Thr390delinsLysTer) rs1554907767
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.124T>C (p.Cys42Arg) rs797044996
NM_005097.4(LGI1):c.124T>G (p.Cys42Gly) rs797044996
NM_005097.4(LGI1):c.1256T>G (p.Leu419Ter) rs1554907787
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.136T>C (p.Cys46Arg) rs104894166
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.1418C>T (p.Ser473Leu) rs797044999
NM_005097.4(LGI1):c.1420C>T (p.Arg474Ter) rs797044998
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.1580_1581del (p.His527fs)
NM_005097.4(LGI1):c.1597C>T (p.Arg533Cys)
NM_005097.4(LGI1):c.1652T>C (p.Val551Ala)
NM_005097.4(LGI1):c.1668C>T (p.Ser556=) rs763654125
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.1A>G (p.Met1Val) rs202204627
NM_005097.4(LGI1):c.205G>A (p.Val69Ile)
NM_005097.4(LGI1):c.215+7C>T
NM_005097.4(LGI1):c.216-55T>C rs143132529
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.303C>T (p.Asn101=) rs762343857
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.360-3C>A
NM_005097.4(LGI1):c.365T>A (p.Ile122Lys) rs119488100
NM_005097.4(LGI1):c.386C>G (p.Ser129Ter) rs1564845068
NM_005097.4(LGI1):c.398A>G (p.His133Arg) rs376452111
NM_005097.4(LGI1):c.406C>T (p.Arg136Trp) rs119488099
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.504-1G>T rs1564851314
NM_005097.4(LGI1):c.600C>T (p.Cys200=) rs148862146
NM_005097.4(LGI1):c.618C>T (p.Tyr206=) rs1554907108
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.657= (p.Phe219=) rs1111820
NM_005097.4(LGI1):c.674-5dup rs1467827240
NM_005097.4(LGI1):c.688C>T (p.Gln230Ter) rs1060502054
NM_005097.4(LGI1):c.695T>C (p.Leu232Pro) rs104894167
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.758del (p.Ala253fs) rs797044997
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+10G>A rs756267808
NM_005097.4(LGI1):c.838+11C>T rs886047486
NM_005097.4(LGI1):c.882G>A (p.Gln294=) rs1554907709
NM_005097.4(LGI1):c.953T>G (p.Phe318Cys) rs28939075

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