ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 211
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579 0.00093
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819 0.00078
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811 0.00064
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862 0.00052
NM_001105206.3(LAMA4):c.2398C>T (p.Arg800Cys) rs202184174 0.00051
NM_001105206.3(LAMA4):c.3055T>C (p.Tyr1019His) rs73532636 0.00048
NM_001105206.3(LAMA4):c.254A>G (p.Asn85Ser) rs145301300 0.00043
NM_001105206.3(LAMA4):c.2614C>G (p.Pro872Ala) rs180931319 0.00028
NM_001105206.3(LAMA4):c.4436G>A (p.Arg1479His) rs140346737 0.00028
NM_001105206.3(LAMA4):c.503G>A (p.Arg168Lys) rs200368819 0.00023
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442 0.00022
NM_001105206.3(LAMA4):c.578C>T (p.Ser193Leu) rs147870828 0.00022
NM_001105206.3(LAMA4):c.4852C>T (p.Leu1618Phe) rs397516733 0.00020
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093 0.00016
NM_001105206.3(LAMA4):c.1298G>A (p.Arg433His) rs369658574 0.00015
NM_001105206.3(LAMA4):c.4792G>T (p.Ala1598Ser) rs202176359 0.00015
NM_001105206.3(LAMA4):c.1541G>A (p.Arg514Gln) rs146358872 0.00014
NM_001105206.3(LAMA4):c.4493G>A (p.Arg1498His) rs147556641 0.00014
NM_001105206.3(LAMA4):c.1277T>C (p.Met426Thr) rs200112094 0.00013
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207 0.00013
NM_001105206.3(LAMA4):c.3043G>C (p.Val1015Leu) rs730880122 0.00013
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320 0.00012
NM_001105206.3(LAMA4):c.1788C>A (p.Asp596Glu) rs145986920 0.00011
NM_001105206.3(LAMA4):c.3283-3C>G rs374159760 0.00011
NM_001105206.3(LAMA4):c.5345G>A (p.Arg1782His) rs782638314 0.00011
NM_001105206.3(LAMA4):c.952A>G (p.Ile318Val) rs141372605 0.00011
NM_001105206.3(LAMA4):c.3817T>C (p.Phe1273Leu) rs781966924 0.00009
NM_001105206.3(LAMA4):c.1522G>A (p.Ala508Thr) rs139730568 0.00008
NM_001105206.3(LAMA4):c.2599C>A (p.Pro867Thr) rs782162498 0.00008
NM_001105206.3(LAMA4):c.4199A>G (p.Tyr1400Cys) rs782041997 0.00008
NM_001105206.3(LAMA4):c.4715T>G (p.Leu1572Arg) rs782367093 0.00008
NM_001105206.3(LAMA4):c.163G>T (p.Val55Leu) rs377370824 0.00007
NM_001105206.3(LAMA4):c.1858G>A (p.Ala620Thr) rs374001056 0.00007
NM_001105206.3(LAMA4):c.2090G>A (p.Arg697His) rs397516723 0.00007
NM_001105206.3(LAMA4):c.5030G>A (p.Arg1677His) rs782174781 0.00007
NM_001105206.3(LAMA4):c.874G>A (p.Glu292Lys) rs781838464 0.00007
NM_001105206.3(LAMA4):c.889G>A (p.Gly297Arg) rs375305822 0.00007
NM_001105206.3(LAMA4):c.1318C>T (p.Arg440Trp) rs140911762 0.00006
NM_001105206.3(LAMA4):c.1420G>A (p.Val474Ile) rs375981026 0.00006
NM_001105206.3(LAMA4):c.1613C>T (p.Ala538Val) rs782569832 0.00006
NM_001105206.3(LAMA4):c.1634G>A (p.Arg545His) rs143937452 0.00006
NM_001105206.3(LAMA4):c.167C>T (p.Ala56Val) rs372763422 0.00006
NM_001105206.3(LAMA4):c.4168C>T (p.Arg1390Trp) rs200189282 0.00006
NM_001105206.3(LAMA4):c.4583G>T (p.Arg1528Leu) rs782805733 0.00006
NM_001105206.3(LAMA4):c.5393T>C (p.Ile1798Thr) rs377204776 0.00006
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329 0.00006
NM_001105206.3(LAMA4):c.547A>G (p.Thr183Ala) rs782667094 0.00006
NM_001105206.3(LAMA4):c.829G>A (p.Val277Ile) rs146225813 0.00006
NM_001105206.3(LAMA4):c.928C>G (p.His310Asp) rs374968791 0.00006
NM_001105206.3(LAMA4):c.1837A>G (p.Met613Val) rs371083384 0.00005
NM_001105206.3(LAMA4):c.2626G>A (p.Glu876Lys) rs147206383 0.00005
NM_001105206.3(LAMA4):c.4208C>T (p.Pro1403Leu) rs1255830395 0.00005
NM_001105206.3(LAMA4):c.4572G>C (p.Leu1524Phe) rs145315273 0.00005
NM_001105206.3(LAMA4):c.1385G>A (p.Arg462Gln) rs781977997 0.00004
NM_001105206.3(LAMA4):c.1769C>G (p.Ala590Gly) rs782394010 0.00004
NM_001105206.3(LAMA4):c.1843G>A (p.Gly615Arg) rs377499201 0.00004
NM_001105206.3(LAMA4):c.2143G>T (p.Ala715Ser) rs140710429 0.00004
NM_001105206.3(LAMA4):c.3165C>T (p.Ser1055=) rs782303510 0.00004
NM_001105206.3(LAMA4):c.3437A>G (p.Asp1146Gly) rs781842093 0.00004
NM_001105206.3(LAMA4):c.3921C>A (p.Tyr1307Ter) rs782630776 0.00004
NM_001105206.3(LAMA4):c.412C>T (p.His138Tyr) rs727503113 0.00004
NM_001105206.3(LAMA4):c.5005A>G (p.Lys1669Glu) rs782716382 0.00004
NM_001105206.3(LAMA4):c.667C>T (p.Arg223Cys) rs372074151 0.00004
NM_001105206.3(LAMA4):c.838C>A (p.Leu280Met) rs369332778 0.00004
NM_001105206.3(LAMA4):c.1275G>T (p.Lys425Asn) rs782618132 0.00003
NM_001105206.3(LAMA4):c.1411T>C (p.Phe471Leu) rs782067046 0.00003
NM_001105206.3(LAMA4):c.1444A>G (p.Asn482Asp) rs782319667 0.00003
NM_001105206.3(LAMA4):c.2096G>A (p.Gly699Asp) rs782786459 0.00003
NM_001105206.3(LAMA4):c.2302C>T (p.His768Tyr) rs140107576 0.00003
NM_001105206.3(LAMA4):c.3585T>A (p.Asp1195Glu) rs786205410 0.00003
NM_001105206.3(LAMA4):c.3697-3C>T rs536295629 0.00003
NM_001105206.3(LAMA4):c.40T>C (p.Trp14Arg) rs782293373 0.00003
NM_001105206.3(LAMA4):c.719-2A>G rs863223691 0.00003
NM_001105206.3(LAMA4):c.964A>C (p.Lys322Gln) rs1375382054 0.00003
NM_001105206.3(LAMA4):c.1559A>G (p.Gln520Arg) rs557735032 0.00002
NM_001105206.3(LAMA4):c.1813A>G (p.Ser605Gly) rs112884471 0.00002
NM_001105206.3(LAMA4):c.1961C>T (p.Ala654Val) rs782806847 0.00002
NM_001105206.3(LAMA4):c.2054C>T (p.Ser685Phe) rs369776441 0.00002
NM_001105206.3(LAMA4):c.3238C>T (p.Arg1080Ter) rs372615994 0.00002
NM_001105206.3(LAMA4):c.3506C>T (p.Pro1169Leu) rs730880123 0.00002
NM_001105206.3(LAMA4):c.3559G>A (p.Ala1187Thr) rs781943786 0.00002
NM_001105206.3(LAMA4):c.4274G>A (p.Ser1425Asn) rs782173105 0.00002
NM_001105206.3(LAMA4):c.475G>A (p.Glu159Lys) rs540626879 0.00002
NM_001105206.3(LAMA4):c.1297C>T (p.Arg433Cys) rs1405779338 0.00001
NM_001105206.3(LAMA4):c.1319G>A (p.Arg440Gln) rs1052880266 0.00001
NM_001105206.3(LAMA4):c.1331A>G (p.Asp444Gly) rs200337032 0.00001
NM_001105206.3(LAMA4):c.1357+1G>A rs1057524730 0.00001
NM_001105206.3(LAMA4):c.1408C>G (p.Leu470Val) rs782742484 0.00001
NM_001105206.3(LAMA4):c.1436A>T (p.Asp479Val) rs781939403 0.00001
NM_001105206.3(LAMA4):c.1455G>T (p.Leu485Phe) rs782305599 0.00001
NM_001105206.3(LAMA4):c.1778A>G (p.His593Arg) rs751004946 0.00001
NM_001105206.3(LAMA4):c.196-2A>C rs1784631494 0.00001
NM_001105206.3(LAMA4):c.1994A>C (p.His665Pro) rs781986112 0.00001
NM_001105206.3(LAMA4):c.203A>G (p.Asn68Ser) rs782428669 0.00001
NM_001105206.3(LAMA4):c.2057-2A>T rs1780342227 0.00001
NM_001105206.3(LAMA4):c.2141A>G (p.Asp714Gly) rs782705506 0.00001
NM_001105206.3(LAMA4):c.2146G>A (p.Val716Ile) rs141742906 0.00001
NM_001105206.3(LAMA4):c.2177A>T (p.Asp726Val) rs781823199 0.00001
NM_001105206.3(LAMA4):c.2188C>T (p.Arg730Cys) rs782482395 0.00001
NM_001105206.3(LAMA4):c.2203A>G (p.Arg735Gly) rs552625719 0.00001
NM_001105206.3(LAMA4):c.227C>T (p.Ser76Leu) rs1554358711 0.00001
NM_001105206.3(LAMA4):c.2283C>G (p.Asn761Lys) rs1554334972 0.00001
NM_001105206.3(LAMA4):c.2305T>C (p.Phe769Leu) rs1554334959 0.00001
NM_001105206.3(LAMA4):c.2309A>G (p.Asp770Gly) rs1179713276 0.00001
NM_001105206.3(LAMA4):c.2465T>C (p.Ile822Thr) rs369962703 0.00001
NM_001105206.3(LAMA4):c.2506A>G (p.Met836Val) rs184539670 0.00001
NM_001105206.3(LAMA4):c.2576C>T (p.Thr859Met) rs730880121 0.00001
NM_001105206.3(LAMA4):c.2620C>G (p.Leu874Val) rs782635471 0.00001
NM_001105206.3(LAMA4):c.3026C>A (p.Ala1009Asp) rs199618820 0.00001
NM_001105206.3(LAMA4):c.3074A>G (p.Tyr1025Cys) rs370557242 0.00001
NM_001105206.3(LAMA4):c.3109C>T (p.Arg1037Ter) rs782727584 0.00001
NM_001105206.3(LAMA4):c.3245C>T (p.Pro1082Leu) rs782040284 0.00001
NM_001105206.3(LAMA4):c.3308G>A (p.Arg1103His) rs782568532 0.00001
NM_001105206.3(LAMA4):c.3311A>G (p.Asn1104Ser) rs542157463 0.00001
NM_001105206.3(LAMA4):c.355G>A (p.Gly119Arg) rs147016335 0.00001
NM_001105206.3(LAMA4):c.370G>C (p.Gly124Arg) rs782530521 0.00001
NM_001105206.3(LAMA4):c.3793A>G (p.Thr1265Ala) rs1179163721 0.00001
NM_001105206.3(LAMA4):c.3986A>G (p.Asp1329Gly) rs1172546960 0.00001
NM_001105206.3(LAMA4):c.4111A>C (p.Ile1371Leu) rs974775253 0.00001
NM_001105206.3(LAMA4):c.4328C>T (p.Ala1443Val) rs782696599 0.00001
NM_001105206.3(LAMA4):c.4513C>T (p.His1505Tyr) rs1554325797 0.00001
NM_001105206.3(LAMA4):c.4607G>T (p.Gly1536Val) rs368316926 0.00001
NM_001105206.3(LAMA4):c.4708G>T (p.Asp1570Tyr) rs199938033 0.00001
NM_001105206.3(LAMA4):c.4724T>C (p.Leu1575Pro) rs372502180 0.00001
NM_001105206.3(LAMA4):c.4786G>A (p.Gly1596Ser) rs373949918 0.00001
NM_001105206.3(LAMA4):c.4883T>G (p.Ile1628Ser) rs145001856 0.00001
NM_001105206.3(LAMA4):c.5206+1G>A rs368035482 0.00001
NM_001105206.3(LAMA4):c.59C>T (p.Ala20Val) rs1060500981 0.00001
NM_001105206.3(LAMA4):c.640C>T (p.Arg214Cys) rs148801194 0.00001
NM_001105206.3(LAMA4):c.676C>T (p.Pro226Ser) rs201820268 0.00001
NM_001105206.3(LAMA4):c.757G>A (p.Gly253Arg) rs377633183 0.00001
NM_001105206.3(LAMA4):c.832T>C (p.Trp278Arg) rs201486893 0.00001
NM_001105206.3(LAMA4):c.944A>G (p.Asn315Ser) rs1029188462 0.00001
NM_001105206.3(LAMA4):c.106A>G (p.Ile36Val) rs727503116
NM_001105206.3(LAMA4):c.1077+11A>G rs782302045
NM_001105206.3(LAMA4):c.1077+5G>A
NM_001105206.3(LAMA4):c.1087G>C (p.Ala363Pro) rs201431982
NM_001105206.3(LAMA4):c.1127A>G (p.Asp376Gly) rs782061102
NM_001105206.3(LAMA4):c.1131del (p.Ile378fs) rs863223693
NM_001105206.3(LAMA4):c.1163C>A (p.Ala388Asp) rs1355664776
NM_001105206.3(LAMA4):c.1176_1177insT (p.Asp393Ter) rs2114895179
NM_001105206.3(LAMA4):c.1227T>G (p.His409Gln) rs1554343372
NM_001105206.3(LAMA4):c.1313C>G (p.Thr438Ser) rs781963976
NM_001105206.3(LAMA4):c.1318C>G (p.Arg440Gly) rs140911762
NM_001105206.3(LAMA4):c.1357+5G>A
NM_001105206.3(LAMA4):c.1384C>T (p.Arg462Trp)
NM_001105206.3(LAMA4):c.1437_1442dup (p.Asp480_Tyr481dup) rs782294432
NM_001105206.3(LAMA4):c.1540C>T (p.Arg514Trp)
NM_001105206.3(LAMA4):c.157C>A (p.Pro53Thr) rs782656592
NM_001105206.3(LAMA4):c.1621_1622del (p.Leu541fs)
NM_001105206.3(LAMA4):c.1777C>T (p.His593Tyr)
NM_001105206.3(LAMA4):c.195+71_195+73del rs786205414
NM_001105206.3(LAMA4):c.200G>A (p.Cys67Tyr) rs1239642838
NM_001105206.3(LAMA4):c.2105_2106dup (p.Ala703Ter) rs1562665452
NM_001105206.3(LAMA4):c.2172_2173del (p.Asp726fs)
NM_001105206.3(LAMA4):c.2174G>C (p.Gly725Ala)
NM_001105206.3(LAMA4):c.2231C>T (p.Thr744Met)
NM_001105206.3(LAMA4):c.22C>T (p.Arg8Cys)
NM_001105206.3(LAMA4):c.2342C>A (p.Ala781Asp) rs863223685
NM_001105206.3(LAMA4):c.2384T>C (p.Leu795Pro) rs2114722043
NM_001105206.3(LAMA4):c.2417G>A (p.Arg806Gln) rs1554334150
NM_001105206.3(LAMA4):c.2932G>A (p.Glu978Lys) rs2114700242
NM_001105206.3(LAMA4):c.3029C>T (p.Thr1010Ile) rs201431614
NM_001105206.3(LAMA4):c.307C>T (p.Arg103Trp) rs138176093
NM_001105206.3(LAMA4):c.308G>A (p.Arg103Gln) rs782029414
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.3126_3140delinsT (p.Thr1043fs) rs2114691399
NM_001105206.3(LAMA4):c.3136C>G (p.Arg1046Gly) rs863223688
NM_001105206.3(LAMA4):c.328T>G (p.Cys110Gly) rs1583890498
NM_001105206.3(LAMA4):c.3322C>T (p.His1108Tyr) rs201660110
NM_001105206.3(LAMA4):c.3343T>C (p.Phe1115Leu) rs1459931996
NM_001105206.3(LAMA4):c.3356C>A (p.Pro1119His) rs1050349
NM_001105206.3(LAMA4):c.3415-3C>A rs2114666342
NM_001105206.3(LAMA4):c.3517A>G (p.Ile1173Val)
NM_001105206.3(LAMA4):c.3558-2A>T rs1583672356
NM_001105206.3(LAMA4):c.371G>A (p.Gly124Glu) rs1562733361
NM_001105206.3(LAMA4):c.3794C>T (p.Thr1265Ile) rs2114656127
NM_001105206.3(LAMA4):c.3819C>A (p.Phe1273Leu) rs138232283
NM_001105206.3(LAMA4):c.3854C>T (p.Ser1285Leu) rs2114646926
NM_001105206.3(LAMA4):c.406del (p.Leu136fs) rs782372455
NM_001105206.3(LAMA4):c.4150G>A (p.Glu1384Lys) rs863223689
NM_001105206.3(LAMA4):c.4169G>A (p.Arg1390Gln) rs200468893
NM_001105206.3(LAMA4):c.4181A>C (p.Lys1394Thr) rs2114635144
NM_001105206.3(LAMA4):c.4226T>C (p.Leu1409Ser) rs1778863428
NM_001105206.3(LAMA4):c.4234C>T (p.Leu1412Phe) rs868967763
NM_001105206.3(LAMA4):c.4275del (p.Gln1426fs) rs2114634490
NM_001105206.3(LAMA4):c.4292G>A (p.Gly1431Glu)
NM_001105206.3(LAMA4):c.4466T>C (p.Phe1489Ser)
NM_001105206.3(LAMA4):c.452G>A (p.Gly151Glu) rs1338209774
NM_001105206.3(LAMA4):c.4582C>T (p.Arg1528Cys)
NM_001105206.3(LAMA4):c.4583G>A (p.Arg1528His) rs782805733
NM_001105206.3(LAMA4):c.4683_4684del (p.Arg1562fs) rs1554325284
NM_001105206.3(LAMA4):c.4967G>A (p.Gly1656Glu) rs41289900
NM_001105206.3(LAMA4):c.4968A>G (p.Gly1656=) rs1778106910
NM_001105206.3(LAMA4):c.5126T>C (p.Val1709Ala) rs1777912190
NM_001105206.3(LAMA4):c.5172G>T (p.Gln1724His) rs2114556816
NM_001105206.3(LAMA4):c.5230C>T (p.Gln1744Ter) rs1554322478
NM_001105206.3(LAMA4):c.528C>G (p.Asn176Lys)
NM_001105206.3(LAMA4):c.5309T>C (p.Phe1770Ser) rs782498118
NM_001105206.3(LAMA4):c.5342C>T (p.Pro1781Leu) rs2114528955
NM_001105206.3(LAMA4):c.5369C>T (p.Thr1790Ile) rs786205409
NM_001105206.3(LAMA4):c.56C>T (p.Ala19Val)
NM_001105206.3(LAMA4):c.673G>A (p.Ala225Thr) rs782121531
NM_001105206.3(LAMA4):c.710A>T (p.Asn237Ile) rs1554349049
NM_001105206.3(LAMA4):c.795C>A (p.Gly265=) rs1484189768
NM_001105206.3(LAMA4):c.815-2A>G rs782687805
NM_001105206.3(LAMA4):c.82G>A (p.Asp28Asn)
NM_001105206.3(LAMA4):c.962T>C (p.Leu321Pro) rs1554347065
NM_001105206.3(LAMA4):c.967-5T>G rs863223692
NM_001105206.3(LAMA4):c.97C>G (p.Pro33Ala)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.