ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance for not provided

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Total variants: 86
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1087G>C (p.Ala363Pro) rs201431982
NM_001105206.3(LAMA4):c.1131del (p.Ile378fs) rs863223693
NM_001105206.3(LAMA4):c.1277T>C (p.Met426Thr) rs200112094
NM_001105206.3(LAMA4):c.1298G>A (p.Arg433His) rs369658574
NM_001105206.3(LAMA4):c.1318C>T (p.Arg440Trp) rs140911762
NM_001105206.3(LAMA4):c.1319G>A (p.Arg440Gln) rs1052880266
NM_001105206.3(LAMA4):c.1357+1G>A rs1057524730
NM_001105206.3(LAMA4):c.1385G>A (p.Arg462Gln) rs781977997
NM_001105206.3(LAMA4):c.1420G>A (p.Val474Ile) rs375981026
NM_001105206.3(LAMA4):c.1436A>T (p.Asp479Val) rs781939403
NM_001105206.3(LAMA4):c.1437_1442dup (p.Asp480_Tyr481dup) rs782294432
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579
NM_001105206.3(LAMA4):c.157C>A (p.Pro53Thr) rs782656592
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207
NM_001105206.3(LAMA4):c.1788C>A (p.Asp596Glu) rs145986920
NM_001105206.3(LAMA4):c.1858G>A (p.Ala620Thr) rs374001056
NM_001105206.3(LAMA4):c.195+71_195+73del rs786205414
NM_001105206.3(LAMA4):c.1961C>T (p.Ala654Val) rs782806847
NM_001105206.3(LAMA4):c.203A>G (p.Asn68Ser) rs782428669
NM_001105206.3(LAMA4):c.2141A>G (p.Asp714Gly) rs782705506
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2177A>T (p.Asp726Val) rs781823199
NM_001105206.3(LAMA4):c.2188C>T (p.Arg730Cys) rs782482395
NM_001105206.3(LAMA4):c.2342C>A (p.Ala781Asp) rs863223685
NM_001105206.3(LAMA4):c.2417G>A (p.Arg806Gln) rs1554334150
NM_001105206.3(LAMA4):c.2506A>G (p.Met836Val) rs184539670
NM_001105206.3(LAMA4):c.2599C>A (p.Pro867Thr) rs782162498
NM_001105206.3(LAMA4):c.2614C>G (p.Pro872Ala) rs180931319
NM_001105206.3(LAMA4):c.2620C>G (p.Leu874Val) rs782635471
NM_001105206.3(LAMA4):c.2671A>G (p.Lys891Glu) rs1554333239
NM_001105206.3(LAMA4):c.2779T>G (p.Trp927Gly) rs863223686
NM_001105206.3(LAMA4):c.2840dup (p.Leu947fs) rs886044794
NM_001105206.3(LAMA4):c.2912C>T (p.Ser971Phe) rs781856644
NM_001105206.3(LAMA4):c.3026C>A (p.Ala1009Asp) rs199618820
NM_001105206.3(LAMA4):c.3029C>T (p.Thr1010Ile) rs201431614
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
NM_001105206.3(LAMA4):c.3055T>C (p.Tyr1019His) rs73532636
NM_001105206.3(LAMA4):c.3074A>G (p.Tyr1025Cys) rs370557242
NM_001105206.3(LAMA4):c.307C>T (p.Arg103Trp) rs138176093
NM_001105206.3(LAMA4):c.3122C>A (p.Ala1041Asp) rs863223687
NM_001105206.3(LAMA4):c.3122C>G (p.Ala1041Gly) rs863223687
NM_001105206.3(LAMA4):c.3136C>G (p.Arg1046Gly) rs863223688
NM_001105206.3(LAMA4):c.3165C>T (p.Ser1055=) rs782303510
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093
NM_001105206.3(LAMA4):c.3245C>T (p.Pro1082Leu) rs782040284
NM_001105206.3(LAMA4):c.3322C>T (p.His1108Tyr) rs201660110
NM_001105206.3(LAMA4):c.355G>A (p.Gly119Arg) rs147016335
NM_001105206.3(LAMA4):c.3585T>A (p.Asp1195Glu) rs786205410
NM_001105206.3(LAMA4):c.370G>C (p.Gly124Arg) rs782530521
NM_001105206.3(LAMA4):c.371G>A (p.Gly124Glu) rs1562733361
NM_001105206.3(LAMA4):c.3817T>C (p.Phe1273Leu) rs781966924
NM_001105206.3(LAMA4):c.3819C>A (p.Phe1273Leu) rs138232283
NM_001105206.3(LAMA4):c.3921C>A (p.Tyr1307Ter) rs782630776
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811
NM_001105206.3(LAMA4):c.3986A>G (p.Asp1329Gly) rs1172546960
NM_001105206.3(LAMA4):c.4111A>C (p.Ile1371Leu) rs974775253
NM_001105206.3(LAMA4):c.4150G>A (p.Glu1384Lys) rs863223689
NM_001105206.3(LAMA4):c.4168C>T (p.Arg1390Trp) rs200189282
NM_001105206.3(LAMA4):c.4328C>T (p.Ala1443Val) rs782696599
NM_001105206.3(LAMA4):c.4583G>A (p.Arg1528His) rs782805733
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819
NM_001105206.3(LAMA4):c.4708G>T (p.Asp1570Tyr) rs199938033
NM_001105206.3(LAMA4):c.5005A>G (p.Lys1669Glu) rs782716382
NM_001105206.3(LAMA4):c.5030G>A (p.Arg1677His) rs782174781
NM_001105206.3(LAMA4):c.503G>A (p.Arg168Lys) rs200368819
NM_001105206.3(LAMA4):c.5206+1G>A rs368035482
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320
NM_001105206.3(LAMA4):c.5230C>T (p.Gln1744Ter) rs1554322478
NM_001105206.3(LAMA4):c.5309T>C (p.Phe1770Ser) rs782498118
NM_001105206.3(LAMA4):c.5344C>T (p.Arg1782Cys) rs145897390
NM_001105206.3(LAMA4):c.5345G>A (p.Arg1782His) rs782638314
NM_001105206.3(LAMA4):c.5369C>T (p.Thr1790Ile) rs786205409
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329
NM_001105206.3(LAMA4):c.59C>T (p.Ala20Val) rs1060500981
NM_001105206.3(LAMA4):c.640C>T (p.Arg214Cys) rs148801194
NM_001105206.3(LAMA4):c.676C>T (p.Pro226Ser) rs201820268
NM_001105206.3(LAMA4):c.719-2A>G rs863223691
NM_001105206.3(LAMA4):c.829G>A (p.Val277Ile) rs146225813
NM_001105206.3(LAMA4):c.832T>C (p.Trp278Arg) rs201486893
NM_001105206.3(LAMA4):c.874G>A (p.Glu292Lys) rs781838464
NM_001105206.3(LAMA4):c.889G>A (p.Gly297Arg) rs375305822
NM_001105206.3(LAMA4):c.928C>G (p.His310Asp) rs374968791
NM_001105206.3(LAMA4):c.962T>C (p.Leu321Pro) rs1554347065
NM_001105206.3(LAMA4):c.964A>C (p.Lys322Gln) rs1375382054
NM_001105206.3(LAMA4):c.967-5T>G rs863223692

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