ClinVar Miner

List of variants in gene LAMA4 reported by Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 151
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HGVS dbSNP
NM_001105206.3(LAMA4):c.*1C>T rs148811960
NM_001105206.3(LAMA4):c.1035G>A (p.Thr345=) rs147069572
NM_001105206.3(LAMA4):c.106A>G (p.Ile36Val) rs727503116
NM_001105206.3(LAMA4):c.1077+8dup rs397516713
NM_001105206.3(LAMA4):c.1078-14C>T rs397516714
NM_001105206.3(LAMA4):c.1189+8T>C rs377133875
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515
NM_001105206.3(LAMA4):c.1209C>T (p.Leu403=) rs397516715
NM_001105206.3(LAMA4):c.1298G>A (p.Arg433His) rs369658574
NM_001105206.3(LAMA4):c.1326C>T (p.Leu442=) rs3752580
NM_001105206.3(LAMA4):c.1353C>T (p.Tyr451=) rs782546070
NM_001105206.3(LAMA4):c.1357+4G>T rs6917763
NM_001105206.3(LAMA4):c.1358-12A>G rs397516716
NM_001105206.3(LAMA4):c.1374G>A (p.Glu458=) rs397516717
NM_001105206.3(LAMA4):c.1390C>G (p.His464Asp) rs151119304
NM_001105206.3(LAMA4):c.140C>T (p.Pro47Leu) rs727503115
NM_001105206.3(LAMA4):c.141G>A (p.Pro47=) rs141926228
NM_001105206.3(LAMA4):c.1444A>G (p.Asn482Asp)
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579
NM_001105206.3(LAMA4):c.1492T>C (p.Tyr498His) rs1050348
NM_001105206.3(LAMA4):c.1503T>A (p.Asp501Glu) rs370194991
NM_001105206.3(LAMA4):c.1551+4C>T rs201209516
NM_001105206.3(LAMA4):c.1551+5A>G rs1554342189
NM_001105206.3(LAMA4):c.1614G>A (p.Ala538=) rs143587921
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075
NM_001105206.3(LAMA4):c.1647A>C (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1668+9G>A rs201457182
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207
NM_001105206.3(LAMA4):c.1674G>A (p.Ala558=) rs150809897
NM_001105206.3(LAMA4):c.1710T>C (p.Ser570=) rs3752577
NM_001105206.3(LAMA4):c.1922C>G (p.Ala641Gly) rs397516718
NM_001105206.3(LAMA4):c.195+131C>G rs138579810
NM_001105206.3(LAMA4):c.195+144T>C rs147118520
NM_001105206.3(LAMA4):c.195+4_195+5del rs397516719
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044
NM_001105206.3(LAMA4):c.196-12T>C rs78871662
NM_001105206.3(LAMA4):c.196-15G>C rs371906362
NM_001105206.3(LAMA4):c.196-9C>T rs144850734
NM_001105206.3(LAMA4):c.1988T>C (p.Ile663Thr) rs538726706
NM_001105206.3(LAMA4):c.1999G>T (p.Asp667Tyr) rs397516720
NM_001105206.3(LAMA4):c.2026G>A (p.Ala676Thr) rs397516721
NM_001105206.3(LAMA4):c.2056+12C>T rs397516722
NM_001105206.3(LAMA4):c.2090G>A (p.Arg697His) rs397516723
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2215G>A (p.Glu739Lys) rs727504935
NM_001105206.3(LAMA4):c.2225A>G (p.Asn742Ser) rs374279330
NM_001105206.3(LAMA4):c.228G>A (p.Ser76=) rs200589775
NM_001105206.3(LAMA4):c.2403G>A (p.Thr801=) rs142559688
NM_001105206.3(LAMA4):c.2493+15G>T rs77901141
NM_001105206.3(LAMA4):c.254A>G (p.Asn85Ser) rs145301300
NM_001105206.3(LAMA4):c.2569G>A (p.Ala857Thr) rs144123257
NM_001105206.3(LAMA4):c.2577G>A (p.Thr859=) rs397516724
NM_001105206.3(LAMA4):c.2640G>T (p.Gln880His) rs397516725
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073
NM_001105206.3(LAMA4):c.267C>T (p.Asn89=) rs727503114
NM_001105206.3(LAMA4):c.2758G>A (p.Asp920Asn) rs727503112
NM_001105206.3(LAMA4):c.2782C>A (p.Pro928Thr) rs727505130
NM_001105206.3(LAMA4):c.279C>T (p.Asp93=) rs397516726
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917
NM_001105206.3(LAMA4):c.2810A>G (p.Glu937Gly) rs35605307
NM_001105206.3(LAMA4):c.2940A>C (p.Thr980=) rs397516727
NM_001105206.3(LAMA4):c.2950G>A (p.Val984Ile) rs145648026
NM_001105206.3(LAMA4):c.297+8G>A rs200595773
NM_001105206.3(LAMA4):c.2977-5C>T rs1554332652
NM_001105206.3(LAMA4):c.3003C>T (p.Gly1001=) rs397516728
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
NM_001105206.3(LAMA4):c.3087C>T (p.Pro1029=) rs146880158
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902
NM_001105206.3(LAMA4):c.3283-15C>T rs2032568
NM_001105206.3(LAMA4):c.3349G>A (p.Gly1117Ser) rs2032567
NM_001105206.3(LAMA4):c.3356C>G (p.Pro1119Arg) rs1050349
NM_001105206.3(LAMA4):c.3357T>G (p.Pro1119=) rs782316528
NM_001105206.3(LAMA4):c.3375G>A (p.Thr1125=) rs143728627
NM_001105206.3(LAMA4):c.3434A>G (p.Asn1145Ser) rs377528058
NM_001105206.3(LAMA4):c.343G>A (p.Asp115Asn) rs781919095
NM_001105206.3(LAMA4):c.3515A>G (p.Asp1172Gly) rs1554330855
NM_001105206.3(LAMA4):c.3558-7T>C rs200864778
NM_001105206.3(LAMA4):c.3819C>T (p.Phe1273=) rs138232283
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342
NM_001105206.3(LAMA4):c.3897A>G (p.Lys1299=) rs876657482
NM_001105206.3(LAMA4):c.392C>T (p.Pro131Leu) rs374273620
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811
NM_001105206.3(LAMA4):c.398C>G (p.Pro133Arg) rs876657842
NM_001105206.3(LAMA4):c.4052A>G (p.Lys1351Arg) rs876657843
NM_001105206.3(LAMA4):c.4065C>T (p.Phe1355=) rs34753919
NM_001105206.3(LAMA4):c.412C>T (p.His138Tyr) rs727503113
NM_001105206.3(LAMA4):c.4168C>T (p.Arg1390Trp) rs200189282
NM_001105206.3(LAMA4):c.4173T>C (p.Tyr1391=) rs35042032
NM_001105206.3(LAMA4):c.423-10C>T rs75058449
NM_001105206.3(LAMA4):c.423-4T>G rs79008328
NM_001105206.3(LAMA4):c.4287+15C>T rs116361180
NM_001105206.3(LAMA4):c.4305T>C (p.Asp1435=) rs147800037
NM_001105206.3(LAMA4):c.4314A>C (p.Ser1438=) rs77367833
NM_001105206.3(LAMA4):c.4386C>T (p.Ser1462=) rs397516729
NM_001105206.3(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595
NM_001105206.3(LAMA4):c.4436G>A (p.Arg1479His) rs140346737
NM_001105206.3(LAMA4):c.4446T>G (p.Phe1482Leu) rs397516730
NM_001105206.3(LAMA4):c.4455A>C (p.Leu1485Phe) rs1554326282
NM_001105206.3(LAMA4):c.4476-3C>A rs397516731
NM_001105206.3(LAMA4):c.4476-4C>A rs727505042
NM_001105206.3(LAMA4):c.456T>A (p.Ala152=) rs149106800
NM_001105206.3(LAMA4):c.460C>T (p.Arg154Trp) rs11757455
NM_001105206.3(LAMA4):c.4626T>C (p.Ile1542=) rs150791451
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442
NM_001105206.3(LAMA4):c.4646A>G (p.Asn1549Ser) rs12110554
NM_001105206.3(LAMA4):c.465C>T (p.Cys155=) rs150354594
NM_001105206.3(LAMA4):c.4665+15G>A rs377415750
NM_001105206.3(LAMA4):c.4665+8G>T rs184220860
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819
NM_001105206.3(LAMA4):c.4679G>A (p.Arg1560Gln) rs397516732
NM_001105206.3(LAMA4):c.4683_4684del (p.Arg1562fs) rs1554325284
NM_001105206.3(LAMA4):c.4691G>T (p.Ser1564Ile) rs369887291
NM_001105206.3(LAMA4):c.4696C>T (p.Arg1566Ter) rs1554325261
NM_001105206.3(LAMA4):c.4716C>T (p.Leu1572=) rs35679345
NM_001105206.3(LAMA4):c.4792G>T (p.Ala1598Ser) rs202176359
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048
NM_001105206.3(LAMA4):c.4852C>T (p.Leu1618Phe) rs397516733
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734
NM_001105206.3(LAMA4):c.4982-3del rs727505356
NM_001105206.3(LAMA4):c.5002T>C (p.Leu1668=) rs369799390
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488
NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=) rs1050353
NM_001105206.3(LAMA4):c.5207-14G>C rs112265545
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320
NM_001105206.3(LAMA4):c.5241G>A (p.Val1747=) rs375447272
NM_001105206.3(LAMA4):c.5267G>A (p.Gly1756Glu) rs782244308
NM_001105206.3(LAMA4):c.5270C>T (p.Pro1757Leu) rs200177134
NM_001105206.3(LAMA4):c.531C>T (p.Pro177=) rs61742228
NM_001105206.3(LAMA4):c.5326+15A>C rs3734290
NM_001105206.3(LAMA4):c.5326+6T>G rs3734289
NM_001105206.3(LAMA4):c.5344C>T (p.Arg1782Cys) rs145897390
NM_001105206.3(LAMA4):c.5380C>T (p.Arg1794Cys) rs781802725
NM_001105206.3(LAMA4):c.5442C>T (p.Ala1814=) rs200300118
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292
NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr) rs144482486
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_001105206.3(LAMA4):c.651C>T (p.Thr217=) rs2072021
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862
NM_001105206.3(LAMA4):c.848_849= (p.Asp283=) rs71543223
NM_001105206.3(LAMA4):c.849= (p.Asp283=) rs9387061
NM_001105206.3(LAMA4):c.863C>G (p.Ala288Gly) rs150084275
NM_001105206.3(LAMA4):c.888C>T (p.Ser296=) rs17073495
NM_001105206.3(LAMA4):c.90C>T (p.Asn30=) rs542554847
NM_001105206.3(LAMA4):c.921T>G (p.Ala307=) rs186498011
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603
NM_001105206.3(LAMA4):c.967-13C>T rs782148493
NM_001105206.3(LAMA4):c.967-15C>G rs375041786
NM_001105206.3(LAMA4):c.997G>A (p.Ala333Thr) rs576711704

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