ClinVar Miner

List of variants in gene LGI1 reported as uncertain significance by Ambry Genetics

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Total variants: 24
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HGVS dbSNP gnomAD frequency
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.837A>G (p.Thr279=) rs755068491 0.00004
NM_005097.4(LGI1):c.1318G>A (p.Val440Met) rs144400448 0.00003
NM_005097.4(LGI1):c.626G>A (p.Arg209His) rs370151711 0.00002
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.61T>C (p.Tyr21His) rs1485010492 0.00001
NM_005097.4(LGI1):c.680C>T (p.Ala227Val) rs750984349 0.00001
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.43C>T (p.Pro15Ser)
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.869T>G (p.Val290Gly)
NM_005097.4(LGI1):c.925T>A (p.Tyr309Asn) rs1564852896

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