ClinVar Miner

List of variants in gene LAMA4 reported as likely benign by Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen

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Total variants: 24
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1035G>A (p.Thr345=) rs147069572
NM_001105206.3(LAMA4):c.1158G>A (p.Glu386=) rs147894075
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075
NM_001105206.3(LAMA4):c.1669-6C>G rs561096787
NM_001105206.3(LAMA4):c.1674G>A (p.Ala558=) rs150809897
NM_001105206.3(LAMA4):c.195+144T>C rs147118520
NM_001105206.3(LAMA4):c.196-12T>C rs78871662
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2214C>T (p.Thr738=) rs782058486
NM_001105206.3(LAMA4):c.2232G>A (p.Thr744=) rs145489423
NM_001105206.3(LAMA4):c.225G>A (p.Leu75=) rs137948709
NM_001105206.3(LAMA4):c.2403G>A (p.Thr801=) rs142559688
NM_001105206.3(LAMA4):c.2569G>A (p.Ala857Thr) rs144123257
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
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.456T>A (p.Ala152=) rs149106800
NM_001105206.3(LAMA4):c.863C>G (p.Ala288Gly) rs150084275
NM_001105206.3(LAMA4):c.888C>T (p.Ser296=) rs17073495
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603

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