ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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Total variants: 21
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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.1455G>T (p.Leu485Phe) rs782305599
NM_001105206.3(LAMA4):c.1507G>A (p.Glu503Lys) rs782568868
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.1959T>C (p.Asp653=) rs143269044
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2719G>A (p.Val907Ile) rs138030555
NM_001105206.3(LAMA4):c.2762C>A (p.Ser921Tyr) rs782424587
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093
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.5437G>A (p.Gly1813Ser) rs142048329
NM_001105206.3(LAMA4):c.572G>A (p.Gly191Glu) rs782010849
NM_001105206.3(LAMA4):c.652G>A (p.Gly218Arg) rs781829741
NM_001105206.3(LAMA4):c.837C>T (p.Asp279=) rs782335744
NM_001105206.3(LAMA4):c.928C>G (p.His310Asp) rs374968791

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