ClinVar Miner

List of variants in gene LAMA4 studied for Cardiomyopathy

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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515 0.03405
NM_001105206.3(LAMA4):c.4173T>C (p.Tyr1391=) rs35042032 0.01889
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917 0.01717
NM_001105206.3(LAMA4):c.423-10C>T rs75058449 0.01596
NM_001105206.3(LAMA4):c.531C>T (p.Pro177=) rs61742228 0.01462
NM_001105206.3(LAMA4):c.4065C>T (p.Phe1355=) rs34753919 0.01154
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902 0.01045
NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr) rs144482486 0.00228
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180 0.00210
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603 0.00205
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292 0.00174
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075 0.00135
NM_001105206.3(LAMA4):c.4665+8G>T rs184220860 0.00112
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044 0.00074
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519 0.00067
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.2655C>T (p.Leu885=) rs35772073 0.00051
NM_001105206.3(LAMA4):c.*1C>T rs148811960 0.00048
NM_001105206.3(LAMA4):c.921T>G (p.Ala307=) rs186498011 0.00045
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419 0.00044
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122 0.00040
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442 0.00022
NM_001105206.3(LAMA4):c.4852C>T (p.Leu1618Phe) rs397516733 0.00020
NM_001105206.3(LAMA4):c.668G>A (p.Arg223His) rs200017155 0.00019
NM_001105206.3(LAMA4):c.4691G>T (p.Ser1564Ile) rs369887291 0.00018
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093 0.00016
NM_001105206.3(LAMA4):c.3147T>C (p.Ser1049=) rs149203646 0.00015
NM_001105206.3(LAMA4):c.4493G>A (p.Arg1498His) rs147556641 0.00014
NM_001105206.3(LAMA4):c.873C>T (p.Ile291=) rs141611768 0.00014
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207 0.00013
NM_001105206.3(LAMA4):c.3283-3C>G rs374159760 0.00011
NM_001105206.3(LAMA4):c.1390C>G (p.His464Asp) rs151119304 0.00010
NM_001105206.3(LAMA4):c.1821G>A (p.Lys607=) rs374481199 0.00010
NM_001105206.3(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595 0.00008
NM_001105206.3(LAMA4):c.167C>T (p.Ala56Val) rs372763422 0.00006
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342 0.00006
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329 0.00006
NM_001105206.3(LAMA4):c.928C>G (p.His310Asp) rs374968791 0.00006
NM_001105206.3(LAMA4):c.1385G>A (p.Arg462Gln) rs781977997 0.00004
NM_001105206.3(LAMA4):c.2226C>T (p.Asn742=) rs530906240 0.00004
NM_001105206.3(LAMA4):c.513C>T (p.Pro171=) rs140249081 0.00004
NM_001105206.3(LAMA4):c.572G>A (p.Gly191Glu) rs782010849 0.00003
NM_001105206.3(LAMA4):c.652G>A (p.Gly218Arg) rs781829741 0.00003
NM_001105206.3(LAMA4):c.1507G>A (p.Glu503Lys) rs782568868 0.00002
NM_001105206.3(LAMA4):c.1455G>T (p.Leu485Phe) rs782305599 0.00001
NM_001105206.3(LAMA4):c.1726C>G (p.Leu576Val) rs782074007 0.00001
NM_001105206.3(LAMA4):c.1854G>A (p.Gln618=) rs587781014 0.00001
NM_001105206.3(LAMA4):c.2195G>A (p.Gly732Glu) rs781889038 0.00001
NM_001105206.3(LAMA4):c.222C>G (p.Thr74=) rs1784629877 0.00001
NM_001105206.3(LAMA4):c.4111A>C (p.Ile1371Leu) rs974775253 0.00001
NM_001105206.3(LAMA4):c.4476-10C>A rs899288475 0.00001
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734 0.00001
NM_001105206.3(LAMA4):c.5004G>A (p.Leu1668=) rs781868926 0.00001
NM_001105206.3(LAMA4):c.633T>C (p.Asn211=) rs782555068 0.00001
NM_001105206.3(LAMA4):c.837C>T (p.Asp279=) rs782335744 0.00001
NM_001105206.3(LAMA4):c.1140C>T (p.His380=) rs782378476
NM_001105206.3(LAMA4):c.1647A>C (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1842C>G (p.Asn614Lys) rs782388698
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.3095_3103del (p.Ser1032_Pro1034del) rs1779575645
NM_001105206.3(LAMA4):c.3110+10A>C rs1554332565
NM_001105206.3(LAMA4):c.3234A>G (p.Glu1078=) rs1779530897
NM_001105206.3(LAMA4):c.373G>T (p.Ala125Ser) rs529185662
NM_001105206.3(LAMA4):c.4606G>C (p.Gly1536Arg) rs1378834238
NM_001105206.3(LAMA4):c.4914C>T (p.Thr1638=) rs1554324464
NM_001105206.3(LAMA4):c.5269C>T (p.Pro1757Ser) rs782001026
NM_001105206.3(LAMA4):c.738C>T (p.Gly246=) rs782462144

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