ClinVar Miner

List of variants in gene LAMC3 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_006059.4(LAMC3):c.4130C>T (p.Thr1377Ile) rs144662546 0.00189
NM_006059.4(LAMC3):c.2227A>G (p.Asn743Asp) rs36030184 0.00079
NM_006059.4(LAMC3):c.3374C>T (p.Ser1125Leu) rs151213335 0.00078
NM_006059.4(LAMC3):c.1547T>G (p.Val516Gly) rs549607103 0.00054
NM_006059.4(LAMC3):c.3101C>T (p.Thr1034Met) rs149131135 0.00052
NM_006059.4(LAMC3):c.3409G>C (p.Ala1137Pro) rs149766298 0.00041
NM_006059.4(LAMC3):c.514G>A (p.Gly172Ser) rs149767552 0.00039
NM_006059.4(LAMC3):c.290A>G (p.Gln97Arg) rs141758463 0.00031
NM_006059.4(LAMC3):c.1066C>T (p.Arg356Cys) rs138713603 0.00030
NM_006059.4(LAMC3):c.4415G>A (p.Arg1472Gln) rs137894550 0.00029
NM_006059.4(LAMC3):c.340T>G (p.Tyr114Asp) rs764924966 0.00023
NM_006059.4(LAMC3):c.995G>A (p.Arg332His) rs149861552 0.00023
NM_006059.4(LAMC3):c.2390C>T (p.Pro797Leu) rs150965854 0.00018
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.538C>T (p.Arg180Cys) rs146609763 0.00016
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.3743C>T (p.Pro1248Leu) rs143410330 0.00013
NM_006059.4(LAMC3):c.944G>A (p.Arg315Gln) rs45444592 0.00012
NM_006059.4(LAMC3):c.4571C>A (p.Ser1524Tyr) rs139127207 0.00011
NM_006059.4(LAMC3):c.2282C>T (p.Ser761Leu) rs376240028 0.00010
NM_006059.4(LAMC3):c.2546G>T (p.Gly849Val) rs143654398 0.00010
NM_006059.4(LAMC3):c.58G>T (p.Ala20Ser) rs1052741862 0.00010
NM_006059.4(LAMC3):c.908G>A (p.Arg303His) rs775368834 0.00008
NM_006059.4(LAMC3):c.1303G>A (p.Ala435Thr) rs371299880 0.00006
NM_006059.4(LAMC3):c.2350C>T (p.Arg784Trp) rs765925947 0.00006
NM_006059.4(LAMC3):c.2744G>A (p.Arg915Gln) rs749496192 0.00006
NM_006059.4(LAMC3):c.4660C>T (p.Arg1554Cys) rs375971925 0.00006
NM_006059.4(LAMC3):c.871C>T (p.Arg291Trp) rs376335879 0.00006
NM_006059.4(LAMC3):c.1339C>T (p.Arg447Cys) rs777086759 0.00005
NM_006059.4(LAMC3):c.1145C>T (p.Pro382Leu) rs780209733 0.00004
NM_006059.4(LAMC3):c.14C>T (p.Ala5Val) rs1131691691 0.00004
NM_006059.4(LAMC3):c.1963C>T (p.Arg655Trp) rs773028028 0.00004
NM_006059.4(LAMC3):c.2714T>G (p.Phe905Cys) rs149470853 0.00004
NM_006059.4(LAMC3):c.2888G>A (p.Arg963Gln) rs151159947 0.00004
NM_006059.4(LAMC3):c.3566C>T (p.Ala1189Val) rs369839636 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.748A>G (p.Lys250Glu) rs768143050 0.00004
NM_006059.4(LAMC3):c.3272G>A (p.Arg1091Gln) rs376158532 0.00003
NM_006059.4(LAMC3):c.4348C>T (p.Arg1450Cys) rs201785610 0.00003
NM_006059.4(LAMC3):c.4477+3A>G rs202112145 0.00003
NM_006059.4(LAMC3):c.4048C>T (p.Pro1350Ser) rs1176016078 0.00002
NM_006059.4(LAMC3):c.4677C>G (p.Asn1559Lys) rs1216451660 0.00002
NM_006059.4(LAMC3):c.1852C>T (p.Pro618Ser) rs749305389 0.00001
NM_006059.4(LAMC3):c.2675A>G (p.His892Arg) rs756250342 0.00001
NM_006059.4(LAMC3):c.2698C>T (p.Arg900Cys) rs757253079 0.00001
NM_006059.4(LAMC3):c.3041C>T (p.Pro1014Leu) rs774083353 0.00001
NM_006059.4(LAMC3):c.3184G>A (p.Val1062Ile) rs150681325 0.00001
NM_006059.4(LAMC3):c.3499A>G (p.Arg1167Gly) rs561097705 0.00001
NM_006059.4(LAMC3):c.4031-10G>A rs555619019 0.00001
NM_006059.4(LAMC3):c.4319C>T (p.Ala1440Val) rs779499766 0.00001
NM_006059.4(LAMC3):c.4480T>C (p.Ser1494Pro) rs1436078297 0.00001
NM_006059.4(LAMC3):c.557G>A (p.Arg186His) rs145176060 0.00001
NM_006059.4(LAMC3):c.1126C>T (p.Pro376Ser) rs1064796412
NM_006059.4(LAMC3):c.1193C>G (p.Thr398Arg) rs1387535460
NM_006059.4(LAMC3):c.1387C>T (p.Arg463Cys) rs139333395
NM_006059.4(LAMC3):c.142G>T (p.Ala48Ser) rs1195853230
NM_006059.4(LAMC3):c.1567C>T (p.Pro523Ser)
NM_006059.4(LAMC3):c.1865C>T (p.Pro622Leu) rs142041428
NM_006059.4(LAMC3):c.1939G>C (p.Gly647Arg) rs144242690
NM_006059.4(LAMC3):c.231C>G (p.Cys77Trp) rs1833367465
NM_006059.4(LAMC3):c.2407C>T (p.His803Tyr) rs2133312243
NM_006059.4(LAMC3):c.2846G>A (p.Arg949Lys) rs1829992999
NM_006059.4(LAMC3):c.3011C>G (p.Thr1004Arg) rs367843721
NM_006059.4(LAMC3):c.3011C>T (p.Thr1004Met) rs367843721
NM_006059.4(LAMC3):c.3027C>G (p.His1009Gln) rs886041210
NM_006059.4(LAMC3):c.3247C>A (p.Leu1083Ile) rs1170788243
NM_006059.4(LAMC3):c.3361G>A (p.Val1121Met)
NM_006059.4(LAMC3):c.3508_3525dup (p.Ala1170_Ala1175dup) rs767643127
NM_006059.4(LAMC3):c.3764C>T (p.Ser1255Phe)
NM_006059.4(LAMC3):c.4052G>A (p.Arg1351Gln) rs199770640
NM_006059.4(LAMC3):c.42_50dup (p.Pro15_Ala17dup) rs1057520165
NM_006059.4(LAMC3):c.457G>A (p.Ala153Thr)
NM_006059.4(LAMC3):c.463G>A (p.Gly155Ser)
NM_006059.4(LAMC3):c.514G>C (p.Gly172Arg)
NM_006059.4(LAMC3):c.638G>A (p.Arg213Gln)
NM_006059.4(LAMC3):c.658G>C (p.Glu220Gln)
NM_006059.4(LAMC3):c.797C>G (p.Ser266Cys) rs1833836345

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