ClinVar Miner

List of variants in gene LAMC3 reported by Genetic Services Laboratory, University of Chicago

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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_006059.4(LAMC3):c.3244A>G (p.Ser1082Gly) rs2275140 0.75621
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.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.4160C>T (p.Ala1387Val) rs141497885 0.00258
NM_006059.4(LAMC3):c.4130C>T (p.Thr1377Ile) rs144662546 0.00189
NM_006059.4(LAMC3):c.1520-6G>A rs192031352 0.00175
NM_006059.4(LAMC3):c.2066C>T (p.Pro689Leu) rs113443891 0.00123
NM_006059.4(LAMC3):c.558C>T (p.Arg186=) rs2275135 0.00105
NM_006059.4(LAMC3):c.2276G>A (p.Gly759Asp) rs150859618 0.00084
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.2238G>A (p.Ala746=) rs141918703 0.00044
NM_006059.4(LAMC3):c.4338G>A (p.Ala1446=) rs375730811 0.00041
NM_006059.4(LAMC3):c.514G>A (p.Gly172Ser) rs149767552 0.00039
NM_006059.4(LAMC3):c.2201A>T (p.Glu734Val) rs376100801 0.00021
NM_006059.4(LAMC3):c.2351G>A (p.Arg784Gln) rs371815223 0.00019
NM_006059.4(LAMC3):c.1330C>T (p.Arg444Cys) rs140066207 0.00016
NM_006059.4(LAMC3):c.538C>T (p.Arg180Cys) rs146609763 0.00016
NM_006059.4(LAMC3):c.1051C>T (p.Arg351Cys) rs201626968 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.2949C>T (p.Cys983=) rs373660982 0.00008
NM_006059.4(LAMC3):c.4540C>T (p.Arg1514Cys) rs145980204 0.00006
NM_006059.4(LAMC3):c.460G>A (p.Asp154Asn) rs200873204 0.00005
NM_006059.4(LAMC3):c.3192G>T (p.Gln1064His) rs373353612 0.00004
NM_006059.4(LAMC3):c.4614G>A (p.Gln1538=) rs754251028 0.00003
NM_006059.4(LAMC3):c.1907G>A (p.Arg636His) rs753991024 0.00002
NM_006059.4(LAMC3):c.1978C>T (p.Arg660Trp) rs374264939 0.00002
NM_006059.4(LAMC3):c.3019G>A (p.Gly1007Ser) rs141105450 0.00002
NM_006059.4(LAMC3):c.1915G>A (p.Val639Ile) rs370174192 0.00001
NM_006059.4(LAMC3):c.818G>A (p.Cys273Tyr) rs747699617 0.00001
NM_006059.4(LAMC3):c.1865C>G (p.Pro622Arg) rs142041428
NM_006059.4(LAMC3):c.1939G>A (p.Gly647Ser) rs144242690
NM_006059.4(LAMC3):c.2308C>G (p.Arg770Gly) rs3739510
NM_006059.4(LAMC3):c.2836_2853del (p.Ala946_Gln951del) rs2133318070
NM_006059.4(LAMC3):c.3064G>A (p.Glu1022Lys) rs954997195
NM_006059.4(LAMC3):c.3069+8G>T rs563444562
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.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.855A>G (p.Ala285=) rs2275132

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