ClinVar Miner

List of variants in gene LGI1 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_005097.4(LGI1):c.345A>G (p.Pro115=) rs151104648 0.00113
NM_005097.4(LGI1):c.600C>T (p.Cys200=) rs148862146 0.00075
NM_005097.4(LGI1):c.717A>C (p.Ile239=) rs146425212 0.00043
NM_005097.4(LGI1):c.1155A>C (p.Leu385=) rs202148793 0.00026
NM_005097.4(LGI1):c.270G>A (p.Thr90=) rs139862877 0.00020
NM_005097.4(LGI1):c.191C>T (p.Thr64Ile) rs373616721 0.00011
NM_005097.4(LGI1):c.1106C>T (p.Ser369Phe) rs150357603 0.00010
NM_005097.4(LGI1):c.812C>T (p.Thr271Ile) rs140752487 0.00009
NM_005097.4(LGI1):c.1122C>T (p.His374=) rs150515718 0.00006
NM_005097.4(LGI1):c.1290G>A (p.Glu430=) rs139879036 0.00006
NM_005097.4(LGI1):c.1668C>T (p.Ser556=) rs763654125 0.00006
NM_005097.4(LGI1):c.205G>A (p.Val69Ile) rs147469708 0.00006
NM_005097.4(LGI1):c.1392G>A (p.Ser464=) rs148804268 0.00005
NM_005097.4(LGI1):c.310G>A (p.Asp104Asn) rs145675377 0.00005
NM_005097.4(LGI1):c.1368A>G (p.Lys456=) rs369166517 0.00004
NM_005097.4(LGI1):c.1578A>C (p.Thr526=) rs776735038 0.00004
NM_005097.4(LGI1):c.837A>G (p.Thr279=) rs755068491 0.00004
NM_005097.4(LGI1):c.1318G>A (p.Val440Met) rs144400448 0.00003
NM_005097.4(LGI1):c.132C>T (p.Ala44=) rs751847276 0.00003
NM_005097.4(LGI1):c.1459T>C (p.Tyr487His) rs748991956 0.00003
NM_005097.4(LGI1):c.1471A>G (p.Ile491Val) rs756891254 0.00003
NM_005097.4(LGI1):c.1075A>G (p.Ile359Val) rs148263562 0.00002
NM_005097.4(LGI1):c.1220G>A (p.Arg407His) rs201376381 0.00002
NM_005097.4(LGI1):c.626G>A (p.Arg209His) rs370151711 0.00002
NM_005097.4(LGI1):c.1095C>T (p.Asn365=) rs934556455 0.00001
NM_005097.4(LGI1):c.1391C>T (p.Ser464Leu) rs747229730 0.00001
NM_005097.4(LGI1):c.299C>T (p.Ser100Leu) rs1263918669 0.00001
NM_005097.4(LGI1):c.46C>G (p.Leu16Val) rs777973395 0.00001
NM_005097.4(LGI1):c.61T>C (p.Tyr21His) rs1485010492 0.00001
NM_005097.4(LGI1):c.673+5T>C rs1162193591 0.00001
NM_005097.4(LGI1):c.680C>T (p.Ala227Val) rs750984349 0.00001
NM_005097.4(LGI1):c.1014C>T (p.Phe338=)
NM_005097.4(LGI1):c.1097G>C (p.Gly366Ala) rs2059988287
NM_005097.4(LGI1):c.1123G>A (p.Ala375Thr) rs757480776
NM_005097.4(LGI1):c.1169C>T (p.Thr390Ile)
NM_005097.4(LGI1):c.1172C>T (p.Pro391Leu)
NM_005097.4(LGI1):c.1219C>G (p.Arg407Gly) rs759897282
NM_005097.4(LGI1):c.1439_1442del (p.Gln480fs) rs1554907835
NM_005097.4(LGI1):c.288G>T (p.Leu96Phe)
NM_005097.4(LGI1):c.34G>A (p.Ala12Thr)
NM_005097.4(LGI1):c.390T>G (p.Ile130Met)
NM_005097.4(LGI1):c.432-5del rs61662431
NM_005097.4(LGI1):c.432-5dup rs61662431
NM_005097.4(LGI1):c.432-6_432-5del
NM_005097.4(LGI1):c.432-6_432-5dup rs61662431
NM_005097.4(LGI1):c.43C>T (p.Pro15Ser)
NM_005097.4(LGI1):c.504-1G>T rs1564851314
NM_005097.4(LGI1):c.53G>A (p.Arg18Lys)
NM_005097.4(LGI1):c.53G>C (p.Arg18Thr)
NM_005097.4(LGI1):c.602A>C (p.Glu201Ala)
NM_005097.4(LGI1):c.606C>T (p.Gly202=)
NM_005097.4(LGI1):c.673+2T>C
NM_005097.4(LGI1):c.741T>C (p.Asp247=)
NM_005097.4(LGI1):c.869T>G (p.Val290Gly)
NM_005097.4(LGI1):c.925T>A (p.Tyr309Asn) rs1564852896

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