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: 142
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HGVS dbSNP
NM_001105206.2(LAMA4):c.196-12T>C rs78871662
NM_001105206.2(LAMA4):c.2569G>A (p.Ala857Thr) rs144123257
NM_001105206.2(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.2(LAMA4):c.4287+15C>T rs116361180
NM_001105206.2(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595
NM_001105206.2(LAMA4):c.5207-14G>C rs112265545
NM_002290.4(LAMA4):c.*1C>T rs148811960
NM_002290.4(LAMA4):c.1014G>A (p.Thr338=) rs147069572
NM_002290.4(LAMA4):c.1056+8dup rs397516713
NM_002290.4(LAMA4):c.1057-14C>T rs397516714
NM_002290.4(LAMA4):c.1168+8T>C rs377133875
NM_002290.4(LAMA4):c.1169-8C>G rs73538515
NM_002290.4(LAMA4):c.1188C>T (p.Leu396=) rs397516715
NM_002290.4(LAMA4):c.1277G>A (p.Arg426His) rs369658574
NM_002290.4(LAMA4):c.1305C>T (p.Leu435=) rs3752580
NM_002290.4(LAMA4):c.1332C>T (p.Tyr444=) rs782546070
NM_002290.4(LAMA4):c.1336+4G>T rs6917763
NM_002290.4(LAMA4):c.1337-12A>G rs397516716
NM_002290.4(LAMA4):c.1353G>A (p.Glu451=) rs397516717
NM_002290.4(LAMA4):c.1369C>G (p.His457Asp) rs151119304
NM_002290.4(LAMA4):c.1454T>A (p.Leu485His) rs3752579
NM_002290.4(LAMA4):c.1471T>C (p.Tyr491His) rs1050348
NM_002290.4(LAMA4):c.1482T>A (p.Asp494Glu) rs370194991
NM_002290.4(LAMA4):c.1530+4C>T rs201209516
NM_002290.4(LAMA4):c.1530+5A>G rs1554342189
NM_002290.4(LAMA4):c.1593G>A (p.Ala531=) rs143587921
NM_002290.4(LAMA4):c.1612C>T (p.Arg538Cys) rs138153075
NM_002290.4(LAMA4):c.1626A>C (p.Ser542=) rs149459643
NM_002290.4(LAMA4):c.1647+9G>A rs201457182
NM_002290.4(LAMA4):c.1652C>T (p.Ala551Val) rs137893207
NM_002290.4(LAMA4):c.1653G>A (p.Ala551=) rs150809897
NM_002290.4(LAMA4):c.1689T>C (p.Ser563=) rs3752577
NM_002290.4(LAMA4):c.1901C>G (p.Ala634Gly) rs397516718
NM_002290.4(LAMA4):c.1938T>C (p.Asp646=) rs143269044
NM_002290.4(LAMA4):c.196-15G>C rs371906362
NM_002290.4(LAMA4):c.196-9C>T rs144850734
NM_002290.4(LAMA4):c.1967T>C (p.Ile656Thr) rs538726706
NM_002290.4(LAMA4):c.1978G>T (p.Asp660Tyr) rs397516720
NM_002290.4(LAMA4):c.2005G>A (p.Ala669Thr) rs397516721
NM_002290.4(LAMA4):c.2035+12C>T rs397516722
NM_002290.4(LAMA4):c.2069G>A (p.Arg690His) rs397516723
NM_002290.4(LAMA4):c.2150G>A (p.Arg717Lys) rs146868519
NM_002290.4(LAMA4):c.2194G>A (p.Glu732Lys) rs727504935
NM_002290.4(LAMA4):c.2204A>G (p.Asn735Ser) rs374279330
NM_002290.4(LAMA4):c.228G>A (p.Ser76=) rs200589775
NM_002290.4(LAMA4):c.2382G>A (p.Thr794=) rs142559688
NM_002290.4(LAMA4):c.2472+15G>T rs77901141
NM_002290.4(LAMA4):c.254A>G (p.Asn85Ser) rs145301300
NM_002290.4(LAMA4):c.2556G>A (p.Thr852=) rs397516724
NM_002290.4(LAMA4):c.2619G>T (p.Gln873His) rs397516725
NM_002290.4(LAMA4):c.2634C>T (p.Leu878=) rs35772073
NM_002290.4(LAMA4):c.267C>T (p.Asn89=) rs727503114
NM_002290.4(LAMA4):c.2737G>A (p.Asp913Asn) rs727503112
NM_002290.4(LAMA4):c.2761C>A (p.Pro921Thr) rs727505130
NM_002290.4(LAMA4):c.2789A>G (p.Glu930Gly) rs35605307
NM_002290.4(LAMA4):c.279C>T (p.Asp93=) rs397516726
NM_002290.4(LAMA4):c.280G>A (p.Gly94Ser) rs35349917
NM_002290.4(LAMA4):c.2919A>C (p.Thr973=) rs397516727
NM_002290.4(LAMA4):c.2929G>A (p.Val977Ile) rs145648026
NM_002290.4(LAMA4):c.2956-5C>T rs1554332652
NM_002290.4(LAMA4):c.297+8G>A rs200595773
NM_002290.4(LAMA4):c.2982C>T (p.Gly994=) rs397516728
NM_002290.4(LAMA4):c.3033G>T (p.Leu1011Phe) rs183262122
NM_002290.4(LAMA4):c.3066C>T (p.Pro1022=) rs146880158
NM_002290.4(LAMA4):c.3154G>A (p.Val1052Met) rs373650093
NM_002290.4(LAMA4):c.3218G>A (p.Arg1073Gln) rs41289902
NM_002290.4(LAMA4):c.3262-15C>T rs2032568
NM_002290.4(LAMA4):c.3328G>A (p.Gly1110Ser) rs2032567
NM_002290.4(LAMA4):c.3335C>G (p.Pro1112Arg) rs1050349
NM_002290.4(LAMA4):c.3336T>G (p.Pro1112=) rs782316528
NM_002290.4(LAMA4):c.3354G>A (p.Thr1118=) rs143728627
NM_002290.4(LAMA4):c.3413A>G (p.Asn1138Ser) rs377528058
NM_002290.4(LAMA4):c.343G>A (p.Asp115Asn) rs781919095
NM_002290.4(LAMA4):c.3494A>G (p.Asp1165Gly) rs1554330855
NM_002290.4(LAMA4):c.3537-7T>C rs200864778
NM_002290.4(LAMA4):c.3798C>T (p.Phe1266=) rs138232283
NM_002290.4(LAMA4):c.3813G>A (p.Gly1271=) rs141988342
NM_002290.4(LAMA4):c.3876A>G (p.Lys1292=) rs876657482
NM_002290.4(LAMA4):c.3922G>A (p.Val1308Ile) rs70940811
NM_002290.4(LAMA4):c.392C>T (p.Pro131Leu) rs374273620
NM_002290.4(LAMA4):c.398C>G (p.Pro133Arg) rs876657842
NM_002290.4(LAMA4):c.4031A>G (p.Lys1344Arg) rs876657843
NM_002290.4(LAMA4):c.4044C>T (p.Phe1348=) rs34753919
NM_002290.4(LAMA4):c.412C>T (p.His138Tyr) rs727503113
NM_002290.4(LAMA4):c.4147C>T (p.Arg1383Trp) rs200189282
NM_002290.4(LAMA4):c.4152T>C (p.Tyr1384=) rs35042032
NM_002290.4(LAMA4):c.423-10C>T rs75058449
NM_002290.4(LAMA4):c.423-4T>G rs79008328
NM_002290.4(LAMA4):c.4284T>C (p.Asp1428=) rs147800037
NM_002290.4(LAMA4):c.4293A>C (p.Ser1431=) rs77367833
NM_002290.4(LAMA4):c.4365C>T (p.Ser1455=) rs397516729
NM_002290.4(LAMA4):c.4415G>A (p.Arg1472His) rs140346737
NM_002290.4(LAMA4):c.4425T>G (p.Phe1475Leu) rs397516730
NM_002290.4(LAMA4):c.4434A>C (p.Leu1478Phe) rs1554326282
NM_002290.4(LAMA4):c.4455-3C>A rs397516731
NM_002290.4(LAMA4):c.4455-4C>A rs727505042
NM_002290.4(LAMA4):c.456T>A (p.Ala152=) rs149106800
NM_002290.4(LAMA4):c.4605T>C (p.Ile1535=) rs150791451
NM_002290.4(LAMA4):c.460C>T (p.Arg154Trp) rs11757455
NM_002290.4(LAMA4):c.4624A>T (p.Asn1542Tyr) rs141261442
NM_002290.4(LAMA4):c.4625A>G (p.Asn1542Ser) rs12110554
NM_002290.4(LAMA4):c.4644+15G>A rs377415750
NM_002290.4(LAMA4):c.4644+8G>T rs184220860
NM_002290.4(LAMA4):c.4657C>A (p.Arg1553=) rs150069819
NM_002290.4(LAMA4):c.4658G>A (p.Arg1553Gln) rs397516732
NM_002290.4(LAMA4):c.465C>T (p.Cys155=) rs150354594
NM_002290.4(LAMA4):c.4662_4663delAA (p.Arg1555Glufs) rs1554325284
NM_002290.4(LAMA4):c.4670G>T (p.Ser1557Ile) rs369887291
NM_002290.4(LAMA4):c.4675C>T (p.Arg1559Ter) rs1554325261
NM_002290.4(LAMA4):c.4695C>T (p.Leu1565=) rs35679345
NM_002290.4(LAMA4):c.4771G>T (p.Ala1591Ser) rs202176359
NM_002290.4(LAMA4):c.4801-3C>T rs191447048
NM_002290.4(LAMA4):c.4831C>T (p.Leu1611Phe) rs397516733
NM_002290.4(LAMA4):c.486T>C (p.Ala162=) rs397516734
NM_002290.4(LAMA4):c.4961-3del rs727505356
NM_002290.4(LAMA4):c.4981T>C (p.Leu1661=) rs369799390
NM_002290.4(LAMA4):c.4995T>A (p.Ile1665=) rs148517180
NM_002290.4(LAMA4):c.5139T>A (p.Val1713=) rs1050353
NM_002290.4(LAMA4):c.514G>A (p.Gly172Ser) rs147695488
NM_002290.4(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320
NM_002290.4(LAMA4):c.5220G>A (p.Val1740=) rs375447272
NM_002290.4(LAMA4):c.5246G>A (p.Gly1749Glu) rs782244308
NM_002290.4(LAMA4):c.5249C>T (p.Pro1750Leu) rs200177134
NM_002290.4(LAMA4):c.5305+15A>C rs3734290
NM_002290.4(LAMA4):c.5305+6T>G rs3734289
NM_002290.4(LAMA4):c.531C>T (p.Pro177=) rs61742228
NM_002290.4(LAMA4):c.5323C>T (p.Arg1775Cys) rs145897390
NM_002290.4(LAMA4):c.5359C>T (p.Arg1787Cys) rs781802725
NM_002290.4(LAMA4):c.5421C>T (p.Ala1807=) rs200300118
NM_002290.4(LAMA4):c.5422G>A (p.Val1808Ile) rs3734292
NM_002290.4(LAMA4):c.5429T>C (p.Ile1810Thr) rs144482486
NM_002290.4(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_002290.4(LAMA4):c.651C>T (p.Thr217=) rs2072021
NM_002290.4(LAMA4):c.674C>T (p.Ala225Val) rs149615862
NM_002290.4(LAMA4):c.827_828AC= (p.Asp276=) rs71543223
NM_002290.4(LAMA4):c.828C= (p.Asp276=) rs9387061
NM_002290.4(LAMA4):c.842C>G (p.Ala281Gly) rs150084275
NM_002290.4(LAMA4):c.867C>T (p.Ser289=) rs17073495
NM_002290.4(LAMA4):c.900T>G (p.Ala300=) rs186498011
NM_002290.4(LAMA4):c.903T>C (p.His301=) rs143580603
NM_002290.4(LAMA4):c.946-15C>G rs375041786
NM_002290.4(LAMA4):c.976G>A (p.Ala326Thr) rs576711704

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