ClinVar Miner

List of variants in gene LAMC3 studied for Inborn genetic diseases

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Total variants: 118
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HGVS dbSNP gnomAD frequency
NM_006059.4(LAMC3):c.4561T>G (p.Ser1521Ala) rs117361076 0.01275
NM_006059.4(LAMC3):c.4130C>T (p.Thr1377Ile) rs144662546 0.00189
NM_006059.4(LAMC3):c.2066C>T (p.Pro689Leu) rs113443891 0.00123
NM_006059.4(LAMC3):c.2227A>G (p.Asn743Asp) rs36030184 0.00079
NM_006059.4(LAMC3):c.2987G>A (p.Arg996His) rs113785045 0.00063
NM_006059.4(LAMC3):c.3409G>C (p.Ala1137Pro) rs149766298 0.00041
NM_006059.4(LAMC3):c.4424G>A (p.Arg1475His) rs113354770 0.00033
NM_006059.4(LAMC3):c.1411C>A (p.Pro471Thr) rs150066772 0.00029
NM_006059.4(LAMC3):c.995G>A (p.Arg332His) rs149861552 0.00023
NM_006059.4(LAMC3):c.2468A>G (p.Asn823Ser) rs140325029 0.00017
NM_006059.4(LAMC3):c.1330C>T (p.Arg444Cys) rs140066207 0.00016
NM_006059.4(LAMC3):c.4541G>A (p.Arg1514His) rs148214465 0.00016
NM_006059.4(LAMC3):c.4414C>T (p.Arg1472Trp) rs145848963 0.00015
NM_006059.4(LAMC3):c.1051C>T (p.Arg351Cys) rs201626968 0.00014
NM_006059.4(LAMC3):c.2123C>T (p.Thr708Ile) rs781761519 0.00014
NM_006059.4(LAMC3):c.2230C>T (p.Pro744Ser) rs145508936 0.00014
NM_006059.4(LAMC3):c.236C>T (p.Ala79Val) rs772194826 0.00014
NM_006059.4(LAMC3):c.544G>A (p.Gly182Ser) rs141325432 0.00014
NM_006059.4(LAMC3):c.3124G>A (p.Asp1042Asn) rs147088114 0.00013
NM_006059.4(LAMC3):c.944G>A (p.Arg315Gln) rs45444592 0.00012
NM_006059.4(LAMC3):c.1031G>A (p.Arg344His) rs143795459 0.00009
NM_006059.4(LAMC3):c.4093G>A (p.Val1365Ile) rs148481163 0.00008
NM_006059.4(LAMC3):c.4565C>T (p.Pro1522Leu) rs749575160 0.00008
NM_006059.4(LAMC3):c.835G>A (p.Glu279Lys) rs776309232 0.00008
NM_006059.4(LAMC3):c.2353C>T (p.Arg785Cys) rs144930767 0.00007
NM_006059.4(LAMC3):c.3730G>A (p.Ala1244Thr) rs113975085 0.00007
NM_006059.4(LAMC3):c.2744G>A (p.Arg915Gln) rs749496192 0.00006
NM_006059.4(LAMC3):c.3862G>A (p.Glu1288Lys) rs369682316 0.00006
NM_006059.4(LAMC3):c.1241G>A (p.Arg414His) rs372564761 0.00005
NM_006059.4(LAMC3):c.460G>A (p.Asp154Asn) rs200873204 0.00005
NM_006059.4(LAMC3):c.847G>A (p.Asp283Asn) rs764097156 0.00005
NM_006059.4(LAMC3):c.1145C>T (p.Pro382Leu) rs780209733 0.00004
NM_006059.4(LAMC3):c.1913G>A (p.Arg638His) rs148563273 0.00004
NM_006059.4(LAMC3):c.2968G>A (p.Glu990Lys) rs762908602 0.00004
NM_006059.4(LAMC3):c.3767C>T (p.Pro1256Leu) rs774738544 0.00004
NM_006059.4(LAMC3):c.3848A>G (p.Gln1283Arg) rs1317788138 0.00004
NM_006059.4(LAMC3):c.4127A>C (p.Lys1376Thr) rs200336679 0.00004
NM_006059.4(LAMC3):c.686T>C (p.Val229Ala) rs149485800 0.00004
NM_006059.4(LAMC3):c.1160C>T (p.Ser387Leu) rs751314241 0.00003
NM_006059.4(LAMC3):c.3272G>A (p.Arg1091Gln) rs376158532 0.00003
NM_006059.4(LAMC3):c.3482C>T (p.Ala1161Val) rs537553919 0.00003
NM_006059.4(LAMC3):c.1919G>T (p.Ser640Ile) rs773662739 0.00002
NM_006059.4(LAMC3):c.1978C>T (p.Arg660Trp) rs374264939 0.00002
NM_006059.4(LAMC3):c.3691G>A (p.Glu1231Lys) rs781285633 0.00002
NM_006059.4(LAMC3):c.526G>A (p.Gly176Ser) rs373575232 0.00002
NM_006059.4(LAMC3):c.932G>A (p.Arg311His) rs767954158 0.00002
NM_006059.4(LAMC3):c.1033_1039del (p.Ser345fs) rs1426926688 0.00001
NM_006059.4(LAMC3):c.1186G>A (p.Asp396Asn) rs577338330 0.00001
NM_006059.4(LAMC3):c.1414C>A (p.His472Asn) rs145387373 0.00001
NM_006059.4(LAMC3):c.1915G>A (p.Val639Ile) rs370174192 0.00001
NM_006059.4(LAMC3):c.208G>T (p.Ala70Ser) rs947443865 0.00001
NM_006059.4(LAMC3):c.2236G>A (p.Ala746Thr) rs900991986 0.00001
NM_006059.4(LAMC3):c.2309G>A (p.Arg770Gln) rs755627961 0.00001
NM_006059.4(LAMC3):c.2675A>G (p.His892Arg) rs756250342 0.00001
NM_006059.4(LAMC3):c.3106G>C (p.Gly1036Arg) rs375429576 0.00001
NM_006059.4(LAMC3):c.3199C>T (p.His1067Tyr) rs373548512 0.00001
NM_006059.4(LAMC3):c.4319C>T (p.Ala1440Val) rs779499766 0.00001
NM_006059.4(LAMC3):c.4633G>A (p.Gly1545Ser) rs1057207177 0.00001
NM_006059.4(LAMC3):c.1043A>G (p.His348Arg)
NM_006059.4(LAMC3):c.1054T>C (p.Cys352Arg)
NM_006059.4(LAMC3):c.1262C>A (p.Ser421Ter)
NM_006059.4(LAMC3):c.1262C>T (p.Ser421Leu) rs376262461
NM_006059.4(LAMC3):c.1292C>G (p.Thr431Ser) rs776500074
NM_006059.4(LAMC3):c.1326C>A (p.Asp442Glu)
NM_006059.4(LAMC3):c.1327C>G (p.Pro443Ala)
NM_006059.4(LAMC3):c.1416C>A (p.His472Gln)
NM_006059.4(LAMC3):c.1846G>A (p.Val616Met)
NM_006059.4(LAMC3):c.1865C>G (p.Pro622Arg) rs142041428
NM_006059.4(LAMC3):c.1883T>A (p.Leu628His)
NM_006059.4(LAMC3):c.1964G>A (p.Arg655Gln)
NM_006059.4(LAMC3):c.2260C>A (p.Pro754Thr) rs371563171
NM_006059.4(LAMC3):c.2328C>G (p.His776Gln)
NM_006059.4(LAMC3):c.2381T>C (p.Phe794Ser)
NM_006059.4(LAMC3):c.2388C>A (p.Asp796Glu)
NM_006059.4(LAMC3):c.2451C>A (p.Asp817Glu) rs1829949479
NM_006059.4(LAMC3):c.247C>G (p.Gln83Glu)
NM_006059.4(LAMC3):c.2615G>A (p.Gly872Asp)
NM_006059.4(LAMC3):c.2882G>T (p.Gly961Val)
NM_006059.4(LAMC3):c.2903C>T (p.Ser968Phe)
NM_006059.4(LAMC3):c.2921C>T (p.Ser974Leu)
NM_006059.4(LAMC3):c.2975A>G (p.Tyr992Cys)
NM_006059.4(LAMC3):c.297G>C (p.Glu99Asp)
NM_006059.4(LAMC3):c.3011C>T (p.Thr1004Met) rs367843721
NM_006059.4(LAMC3):c.3143G>A (p.Gly1048Glu)
NM_006059.4(LAMC3):c.3181del (p.Asp1061fs) rs1554789671
NM_006059.4(LAMC3):c.3202C>A (p.Leu1068Met)
NM_006059.4(LAMC3):c.3214G>T (p.Ala1072Ser)
NM_006059.4(LAMC3):c.3250G>A (p.Glu1084Lys) rs146221263
NM_006059.4(LAMC3):c.3250G>C (p.Glu1084Gln) rs146221263
NM_006059.4(LAMC3):c.3379G>A (p.Glu1127Lys) rs140955110
NM_006059.4(LAMC3):c.3393T>G (p.His1131Gln)
NM_006059.4(LAMC3):c.3409G>A (p.Ala1137Thr) rs149766298
NM_006059.4(LAMC3):c.3494G>A (p.Ser1165Asn)
NM_006059.4(LAMC3):c.3613C>T (p.Arg1205Trp) rs1199242853
NM_006059.4(LAMC3):c.3941C>G (p.Ala1314Gly)
NM_006059.4(LAMC3):c.4147A>T (p.Met1383Leu)
NM_006059.4(LAMC3):c.4207G>A (p.Val1403Met) rs1830319598
NM_006059.4(LAMC3):c.4240G>A (p.Ala1414Thr)
NM_006059.4(LAMC3):c.4288A>G (p.Thr1430Ala)
NM_006059.4(LAMC3):c.4295A>G (p.Gln1432Arg)
NM_006059.4(LAMC3):c.4298C>A (p.Thr1433Lys)
NM_006059.4(LAMC3):c.4349G>A (p.Arg1450His)
NM_006059.4(LAMC3):c.4430C>T (p.Ser1477Leu)
NM_006059.4(LAMC3):c.4447G>A (p.Glu1483Lys)
NM_006059.4(LAMC3):c.4497A>C (p.Gln1499His)
NM_006059.4(LAMC3):c.4561T>A (p.Ser1521Thr)
NM_006059.4(LAMC3):c.4562C>A (p.Ser1521Tyr)
NM_006059.4(LAMC3):c.4639G>A (p.Glu1547Lys) rs780728013
NM_006059.4(LAMC3):c.464G>A (p.Gly155Asp)
NM_006059.4(LAMC3):c.671G>T (p.Gly224Val)
NM_006059.4(LAMC3):c.697G>A (p.Glu233Lys) rs1161249325
NM_006059.4(LAMC3):c.763C>T (p.Leu255Phe)
NM_006059.4(LAMC3):c.793T>G (p.Phe265Val)
NM_006059.4(LAMC3):c.848A>T (p.Asp283Val)
NM_006059.4(LAMC3):c.853G>A (p.Ala285Thr)
NM_006059.4(LAMC3):c.958G>A (p.Ala320Thr)
NM_006059.4(LAMC3):c.984C>G (p.Asn328Lys)
NM_006059.4(LAMC3):c.98A>C (p.Gln33Pro)

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