ClinVar Miner

List of variants in gene LAMA4 reported as likely benign for Dilated cardiomyopathy 1JJ

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Total variants: 58
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1035G>A (p.Thr345=) rs147069572
NM_001105206.3(LAMA4):c.1104A>G (p.Gln368=) rs782501242
NM_001105206.3(LAMA4):c.1158G>A (p.Glu386=) rs147894075
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515
NM_001105206.3(LAMA4):c.150G>A (p.Thr50=) rs538596272
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.1821G>A (p.Lys607=) rs374481199
NM_001105206.3(LAMA4):c.195+144T>C rs147118520
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044
NM_001105206.3(LAMA4):c.196-12T>C rs78871662
NM_001105206.3(LAMA4):c.1962G>A (p.Ala654=) rs140246538
NM_001105206.3(LAMA4):c.2097T>C (p.Gly699=) rs1271082359
NM_001105206.3(LAMA4):c.2146G>A (p.Val716Ile) rs141742906
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.2385C>T (p.Leu795=) rs1469242521
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.2769C>T (p.Pro923=) rs782151816
NM_001105206.3(LAMA4):c.279C>T (p.Asp93=) rs397516726
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
NM_001105206.3(LAMA4):c.3055T>C (p.Tyr1019His) rs73532636
NM_001105206.3(LAMA4):c.3087C>T (p.Pro1029=) rs146880158
NM_001105206.3(LAMA4):c.3165C>T (p.Ser1055=) rs782303510
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902
NM_001105206.3(LAMA4):c.3246A>G (p.Pro1082=) rs782387031
NM_001105206.3(LAMA4):c.36T>C (p.Pro12=) rs782309477
NM_001105206.3(LAMA4):c.393G>A (p.Pro131=) rs782691713
NM_001105206.3(LAMA4):c.4065C>T (p.Phe1355=) rs34753919
NM_001105206.3(LAMA4):c.4077A>G (p.Pro1359=) rs1060504123
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.4626T>C (p.Ile1542=) rs150791451
NM_001105206.3(LAMA4):c.4665+8G>T rs184220860
NM_001105206.3(LAMA4):c.4691G>T (p.Ser1564Ile) rs369887291
NM_001105206.3(LAMA4):c.4852C>T (p.Leu1618Phe) rs397516733
NM_001105206.3(LAMA4):c.4872T>C (p.Asn1624=) rs781829296
NM_001105206.3(LAMA4):c.4878C>A (p.Ala1626=) rs1554324481
NM_001105206.3(LAMA4):c.4914C>T (p.Thr1638=) rs1554324464
NM_001105206.3(LAMA4):c.4953T>C (p.Phe1651=) rs1554324452
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488
NM_001105206.3(LAMA4):c.5184T>C (p.Asp1728=) rs782595382
NM_001105206.3(LAMA4):c.5364C>A (p.Pro1788=) rs370510960
NM_001105206.3(LAMA4):c.5442C>T (p.Ala1814=) rs200300118
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862
NM_001105206.3(LAMA4):c.720G>A (p.Val240=) rs781915056
NM_001105206.3(LAMA4):c.730G>C (p.Gly244Arg) rs147078770
NM_001105206.3(LAMA4):c.824A>G (p.Lys275Arg) rs183711657
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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