ClinVar Miner

List of variants in gene LAMC3 reported as likely benign for not specified

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Gene type:
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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_006059.4(LAMC3):c.219T>G (p.His73Gln) rs3739512 0.56936
NM_006059.4(LAMC3):c.1932C>T (p.Ser644=) rs12349966 0.48282
NM_006059.4(LAMC3):c.963C>T (p.Ala321=) rs2275131 0.40359
NM_006059.4(LAMC3):c.4378-4A>G rs4740413 0.38051
NM_006059.4(LAMC3):c.3114C>G (p.Leu1038=) rs10901345 0.33677
NM_006059.4(LAMC3):c.3108G>A (p.Gly1036=) rs10901344 0.33663
NM_006059.4(LAMC3):c.521C>A (p.Pro174His) rs2275137 0.29468
NM_006059.4(LAMC3):c.4298C>T (p.Thr1433Met) rs7024108 0.28739
NM_006059.4(LAMC3):c.1564C>T (p.Pro522Ser) rs869457 0.28273
NM_006059.4(LAMC3):c.4231-10C>T rs4740411 0.20977
NM_006059.4(LAMC3):c.4376G>A (p.Arg1459Gln) rs4740412 0.20674
NM_006059.4(LAMC3):c.1218G>A (p.Thr406=) rs2293518 0.20549
NM_006059.4(LAMC3):c.3507C>T (p.Thr1169=) rs3818800 0.14515
NM_006059.4(LAMC3):c.75C>T (p.Cys25=) rs13286358 0.10217
NM_006059.4(LAMC3):c.1047C>T (p.Gly349=) rs45603838 0.06722
NM_006059.4(LAMC3):c.3790C>T (p.Arg1264Trp) rs11244275 0.04427
NM_006059.4(LAMC3):c.92G>T (p.Arg31Leu) rs116259120 0.02047
NM_006059.4(LAMC3):c.2559C>T (p.Ser853=) rs34652877 0.01902
NM_006059.4(LAMC3):c.-2C>T rs137883250 0.01424
NM_006059.4(LAMC3):c.4561T>G (p.Ser1521Ala) rs117361076 0.01275
NM_006059.4(LAMC3):c.454C>T (p.Arg152Cys) rs45628035 0.00975
NM_006059.4(LAMC3):c.3371C>T (p.Ser1124Phe) rs113259170 0.00738
NM_006059.4(LAMC3):c.2352G>A (p.Arg784=) rs35654564 0.00652
NM_006059.4(LAMC3):c.146A>G (p.Gln49Arg) rs201962705 0.00645
NM_006059.4(LAMC3):c.786G>A (p.Val262=) rs2275133 0.00543
NM_006059.4(LAMC3):c.-39G>A rs533170505 0.00439
NM_006059.4(LAMC3):c.517C>T (p.Arg173Trp) rs145775274 0.00378
NM_006059.4(LAMC3):c.4092C>T (p.Ser1364=) rs141724499 0.00360
NM_006059.4(LAMC3):c.2891-8C>T rs199535979 0.00339
NM_006059.4(LAMC3):c.3069+22C>T rs117621658 0.00303
NM_006059.4(LAMC3):c.2517G>A (p.Thr839=) rs140540789 0.00292
NM_006059.4(LAMC3):c.368G>T (p.Arg123Leu) rs140461419 0.00284
NM_006059.4(LAMC3):c.3927+8C>G rs148008251 0.00228
NM_006059.4(LAMC3):c.3347C>G (p.Ala1116Gly) rs36028197 0.00226
NM_006059.4(LAMC3):c.1520-6G>A rs192031352 0.00175
NM_006059.4(LAMC3):c.3131G>T (p.Gly1044Val) rs114605554 0.00170
NM_006059.4(LAMC3):c.4477+9G>T rs201360815 0.00141
NM_006059.4(LAMC3):c.558C>T (p.Arg186=) rs2275135 0.00105
NM_006059.4(LAMC3):c.4338G>A (p.Ala1446=) rs375730811 0.00041
NM_006059.4(LAMC3):c.1019G>A (p.Arg340Gln) rs149004188 0.00037
NM_006059.4(LAMC3):c.*19G>A rs199668023 0.00022
NM_006059.4(LAMC3):c.1940-10C>T rs373939366 0.00014
NM_006059.4(LAMC3):c.944G>A (p.Arg315Gln) rs45444592 0.00012
NM_006059.4(LAMC3):c.3765C>G (p.Ser1255=) rs148370295 0.00011
NM_006059.4(LAMC3):c.1884C>T (p.Leu628=) rs762552193 0.00009
NM_006059.4(LAMC3):c.2347+18C>T rs372898308 0.00007
NM_006059.4(LAMC3):c.4446C>T (p.Ile1482=) rs200452667 0.00006
NM_006059.3(LAMC3):c.-47C>G rs540983125 0.00005
NM_006059.4(LAMC3):c.1866C>G (p.Pro622=) rs537785027 0.00004
NM_006059.4(LAMC3):c.2718C>T (p.Phe906=) rs774628409 0.00003
NM_006059.4(LAMC3):c.3417+13A>T rs950070867 0.00003
NM_006059.4(LAMC3):c.4614G>A (p.Gln1538=) rs754251028 0.00003
NM_006059.4(LAMC3):c.3276G>A (p.Glu1092=) rs1054281893 0.00002
NM_006059.4(LAMC3):c.1414C>A (p.His472Asn) rs145387373 0.00001
NM_006059.4(LAMC3):c.2308C>A (p.Arg770=) rs3739510
NM_006059.4(LAMC3):c.2308C>G (p.Arg770Gly) rs3739510
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.3897G>C (p.Ala1299=) rs539911303
NM_006059.4(LAMC3):c.4146G>C (p.Arg1382Ser) rs147092908
NM_006059.4(LAMC3):c.4271G>A (p.Arg1424His) rs34724991
NM_006059.4(LAMC3):c.521_522delinsAG (p.Pro174Gln) rs386738954
NM_006059.4(LAMC3):c.522C>G (p.Pro174=) rs2275136
NM_006059.4(LAMC3):c.809+13_809+19del rs763259337
NM_006059.4(LAMC3):c.855A>G (p.Ala285=) rs2275132

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