ClinVar Miner

List of variants in gene LAMA4 studied for Cardiomyopathy

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Total variants: 45
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HGVS dbSNP
NM_001105206.3(LAMA4):c.*1C>T rs148811960
NM_001105206.3(LAMA4):c.1140C>T (p.His380=) rs782378476
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515
NM_001105206.3(LAMA4):c.1455G>T (p.Leu485Phe) rs782305599
NM_001105206.3(LAMA4):c.1507G>A (p.Glu503Lys) rs782568868
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.1673C>T (p.Ala558Val) rs137893207
NM_001105206.3(LAMA4):c.1726C>G (p.Leu576Val) rs782074007
NM_001105206.3(LAMA4):c.1821G>A (p.Lys607=) rs374481199
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2226C>T (p.Asn742=) rs530906240
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2719G>A (p.Val907Ile) rs138030555
NM_001105206.3(LAMA4):c.2745G>A (p.Val915=) rs1554333214
NM_001105206.3(LAMA4):c.2762C>A (p.Ser921Tyr) rs782424587
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917
NM_001105206.3(LAMA4):c.2917C>T (p.Leu973=) rs1554332949
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
NM_001105206.3(LAMA4):c.3147T>C (p.Ser1049=) rs149203646
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.4065C>T (p.Phe1355=) rs34753919
NM_001105206.3(LAMA4):c.4173T>C (p.Tyr1391=) rs35042032
NM_001105206.3(LAMA4):c.423-10C>T rs75058449
NM_001105206.3(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595
NM_001105206.3(LAMA4):c.4606G>C (p.Gly1536Arg) rs1378834238
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442
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.4914C>T (p.Thr1638=) rs1554324464
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180
NM_001105206.3(LAMA4):c.513C>T (p.Pro171=) rs140249081
NM_001105206.3(LAMA4):c.531C>T (p.Pro177=) rs61742228
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292
NM_001105206.3(LAMA4):c.572G>A (p.Gly191Glu) rs782010849
NM_001105206.3(LAMA4):c.633T>C (p.Asn211=) rs782555068
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_001105206.3(LAMA4):c.652G>A (p.Gly218Arg) rs781829741
NM_001105206.3(LAMA4):c.738C>T (p.Gly246=) rs782462144
NM_001105206.3(LAMA4):c.837C>T (p.Asp279=) rs782335744
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603
NM_001105206.3(LAMA4):c.928C>G (p.His310Asp) rs374968791

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