ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance for Cardiomyopathy

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Total variants: 21
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HGVS dbSNP
NM_001105206.2(LAMA4):c.1455G>T (p.Leu485Phe)
NM_001105206.2(LAMA4):c.1507G>A (p.Glu503Lys)
NM_001105206.2(LAMA4):c.1726C>G (p.Leu576Val)
NM_001105206.2(LAMA4):c.2719G>A (p.Val907Ile)
NM_001105206.2(LAMA4):c.2762C>A (p.Ser921Tyr)
NM_001105206.2(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595
NM_001105206.2(LAMA4):c.4606G>C (p.Gly1536Arg)
NM_001105206.2(LAMA4):c.572G>A (p.Gly191Glu)
NM_001105206.2(LAMA4):c.652G>A (p.Gly218Arg)
NM_001105206.2(LAMA4):c.837C>T (p.Asp279=)
NM_002290.4(LAMA4):c.*1C>T rs148811960
NM_002290.4(LAMA4):c.1119C>T (p.His373=) rs782378476
NM_002290.4(LAMA4):c.1652C>T (p.Ala551Val) rs137893207
NM_002290.4(LAMA4):c.1938T>C (p.Asp646=) rs143269044
NM_002290.4(LAMA4):c.2150G>A (p.Arg717Lys) rs146868519
NM_002290.4(LAMA4):c.3033G>T (p.Leu1011Phe) rs183262122
NM_002290.4(LAMA4):c.3154G>A (p.Val1052Met) rs373650093
NM_002290.4(LAMA4):c.4624A>T (p.Asn1542Tyr) rs141261442
NM_002290.4(LAMA4):c.4831C>T (p.Leu1611Phe) rs397516733
NM_002290.4(LAMA4):c.5416G>A (p.Gly1806Ser) rs142048329
NM_002290.4(LAMA4):c.907C>G (p.His303Asp) rs374968791

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