ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance for Dilated cardiomyopathy 1JJ

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Total variants: 115
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1077+4C>T rs1192025877
NM_001105206.3(LAMA4):c.1082dup (p.Asn361fs) rs1562698762
NM_001105206.3(LAMA4):c.1105C>A (p.Leu369Ile) rs1291328403
NM_001105206.3(LAMA4):c.1166A>G (p.His389Arg)
NM_001105206.3(LAMA4):c.1275G>T (p.Lys425Asn) rs782618132
NM_001105206.3(LAMA4):c.1277T>C (p.Met426Thr) rs200112094
NM_001105206.3(LAMA4):c.1298G>A (p.Arg433His) rs369658574
NM_001105206.3(LAMA4):c.1327G>A (p.Val443Met) rs371650107
NM_001105206.3(LAMA4):c.1385G>A (p.Arg462Gln) rs781977997
NM_001105206.3(LAMA4):c.1390C>G (p.His464Asp) rs151119304
NM_001105206.3(LAMA4):c.1420G>A (p.Val474Ile) rs375981026
NM_001105206.3(LAMA4):c.1436A>T (p.Asp479Val) rs781939403
NM_001105206.3(LAMA4):c.1437_1442dup (p.Asp480_Tyr481dup) rs782294432
NM_001105206.3(LAMA4):c.1503T>A (p.Asp501Glu) rs370194991
NM_001105206.3(LAMA4):c.1522G>A (p.Ala508Thr)
NM_001105206.3(LAMA4):c.153C>A (p.Ser51Arg) rs782192817
NM_001105206.3(LAMA4):c.1541G>A (p.Arg514Gln) rs146358872
NM_001105206.3(LAMA4):c.1582G>A (p.Glu528Lys)
NM_001105206.3(LAMA4):c.1595T>C (p.Met532Thr)
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207
NM_001105206.3(LAMA4):c.167C>T (p.Ala56Val) rs372763422
NM_001105206.3(LAMA4):c.1788C>A (p.Asp596Glu) rs145986920
NM_001105206.3(LAMA4):c.1801G>A (p.Ala601Thr)
NM_001105206.3(LAMA4):c.1829G>A (p.Ser610Asn)
NM_001105206.3(LAMA4):c.1843G>A (p.Gly615Arg)
NM_001105206.3(LAMA4):c.1960-3T>C rs373682270
NM_001105206.3(LAMA4):c.1961C>T (p.Ala654Val) rs782806847
NM_001105206.3(LAMA4):c.2090G>A (p.Arg697His) rs397516723
NM_001105206.3(LAMA4):c.2143G>T (p.Ala715Ser) rs140710429
NM_001105206.3(LAMA4):c.2188C>T (p.Arg730Cys) rs782482395
NM_001105206.3(LAMA4):c.2203A>G (p.Arg735Gly) rs552625719
NM_001105206.3(LAMA4):c.2225A>G (p.Asn742Ser) rs374279330
NM_001105206.3(LAMA4):c.2231C>A (p.Thr744Lys)
NM_001105206.3(LAMA4):c.2305T>C (p.Phe769Leu) rs1554334959
NM_001105206.3(LAMA4):c.2398C>T (p.Arg800Cys) rs202184174
NM_001105206.3(LAMA4):c.2402C>T (p.Thr801Met) rs782325644
NM_001105206.3(LAMA4):c.2416C>G (p.Arg806Gly)
NM_001105206.3(LAMA4):c.2527G>C (p.Ala843Pro) rs536755553
NM_001105206.3(LAMA4):c.2576C>T (p.Thr859Met) rs730880121
NM_001105206.3(LAMA4):c.2611C>T (p.Arg871Trp)
NM_001105206.3(LAMA4):c.2747A>T (p.Glu916Val) rs1554333212
NM_001105206.3(LAMA4):c.2977-3T>C rs1391739831
NM_001105206.3(LAMA4):c.3073T>C (p.Tyr1025His) rs1554332595
NM_001105206.3(LAMA4):c.307C>T (p.Arg103Trp) rs138176093
NM_001105206.3(LAMA4):c.3086C>T (p.Pro1029Leu) rs797025921
NM_001105206.3(LAMA4):c.3153C>A (p.Phe1051Leu) rs1060500983
NM_001105206.3(LAMA4):c.3161G>A (p.Gly1054Asp) rs782592337
NM_001105206.3(LAMA4):c.3166G>A (p.Gly1056Ser) rs145321940
NM_001105206.3(LAMA4):c.3238C>T (p.Arg1080Ter) rs372615994
NM_001105206.3(LAMA4):c.3245C>T (p.Pro1082Leu) rs782040284
NM_001105206.3(LAMA4):c.3283-3C>G
NM_001105206.3(LAMA4):c.328T>G (p.Cys110Gly)
NM_001105206.3(LAMA4):c.343G>A (p.Asp115Asn) rs781919095
NM_001105206.3(LAMA4):c.3483G>A (p.Met1161Ile)
NM_001105206.3(LAMA4):c.3557+6G>C rs782019593
NM_001105206.3(LAMA4):c.355G>A (p.Gly119Arg) rs147016335
NM_001105206.3(LAMA4):c.3574C>T (p.Leu1192Phe) rs181787647
NM_001105206.3(LAMA4):c.3742A>G (p.Ile1248Val) rs547323858
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342
NM_001105206.3(LAMA4):c.4052A>G (p.Lys1351Arg) rs876657843
NM_001105206.3(LAMA4):c.4066G>C (p.Gly1356Arg)
NM_001105206.3(LAMA4):c.4078A>G (p.Ile1360Val) rs1219695312
NM_001105206.3(LAMA4):c.40T>C (p.Trp14Arg) rs782293373
NM_001105206.3(LAMA4):c.4111A>C (p.Ile1371Leu) rs974775253
NM_001105206.3(LAMA4):c.4168C>T (p.Arg1390Trp) rs200189282
NM_001105206.3(LAMA4):c.4223C>T (p.Pro1408Leu)
NM_001105206.3(LAMA4):c.4234C>T (p.Leu1412Phe)
NM_001105206.3(LAMA4):c.4235T>C (p.Leu1412Pro) rs376369192
NM_001105206.3(LAMA4):c.4287+4A>G
NM_001105206.3(LAMA4):c.4402C>T (p.His1468Tyr) rs1562631261
NM_001105206.3(LAMA4):c.4409A>T (p.Tyr1470Phe) rs1554326304
NM_001105206.3(LAMA4):c.4436G>A (p.Arg1479His) rs140346737
NM_001105206.3(LAMA4):c.4572G>C (p.Leu1524Phe) rs145315273
NM_001105206.3(LAMA4):c.4583G>A (p.Arg1528His) rs782805733
NM_001105206.3(LAMA4):c.4583G>T (p.Arg1528Leu) rs782805733
NM_001105206.3(LAMA4):c.4601A>G (p.Asn1534Ser) rs782057429
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442
NM_001105206.3(LAMA4):c.4681G>A (p.Glu1561Lys)
NM_001105206.3(LAMA4):c.4724T>C (p.Leu1575Pro)
NM_001105206.3(LAMA4):c.4786G>A (p.Gly1596Ser)
NM_001105206.3(LAMA4):c.4792G>T (p.Ala1598Ser) rs202176359
NM_001105206.3(LAMA4):c.4852C>T (p.Leu1618Phe) rs397516733
NM_001105206.3(LAMA4):c.4870A>C (p.Asn1624His) rs587693487
NM_001105206.3(LAMA4):c.4972G>A (p.Val1658Met) rs149555058
NM_001105206.3(LAMA4):c.5021T>G (p.Phe1674Cys) rs1209180229
NM_001105206.3(LAMA4):c.503G>A (p.Arg168Lys) rs200368819
NM_001105206.3(LAMA4):c.5129A>G (p.Asn1710Ser) rs1219557048
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320
NM_001105206.3(LAMA4):c.5237A>G (p.Asp1746Gly) rs1060500982
NM_001105206.3(LAMA4):c.5254A>G (p.Asn1752Asp)
NM_001105206.3(LAMA4):c.5270C>T (p.Pro1757Leu) rs200177134
NM_001105206.3(LAMA4):c.5393T>C (p.Ile1798Thr) rs377204776
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329
NM_001105206.3(LAMA4):c.5444dup (p.Ser1816fs) rs782327744
NM_001105206.3(LAMA4):c.5458T>C (p.Cys1820Arg) rs782706577
NM_001105206.3(LAMA4):c.547A>G (p.Thr183Ala) rs782667094
NM_001105206.3(LAMA4):c.550T>C (p.Cys184Arg)
NM_001105206.3(LAMA4):c.59C>T (p.Ala20Val) rs1060500981
NM_001105206.3(LAMA4):c.657C>A (p.Phe219Leu) rs1554349095
NM_001105206.3(LAMA4):c.668G>A (p.Arg223His) rs200017155
NM_001105206.3(LAMA4):c.673G>C (p.Ala225Pro)
NM_001105206.3(LAMA4):c.710A>T (p.Asn237Ile) rs1554349049
NM_001105206.3(LAMA4):c.730G>A (p.Gly244Arg) rs147078770
NM_001105206.3(LAMA4):c.829G>A (p.Val277Ile) rs146225813
NM_001105206.3(LAMA4):c.82_84GAC[1] (p.Asp29del) rs781840950
NM_001105206.3(LAMA4):c.874G>A (p.Glu292Lys) rs781838464
NM_001105206.3(LAMA4):c.909T>A (p.Ser303=)
NM_001105206.3(LAMA4):c.913G>A (p.Ala305Thr) rs782325733
NM_001105206.3(LAMA4):c.918C>A (p.Ala306=) rs962353764
NM_001105206.3(LAMA4):c.944A>G (p.Asn315Ser) rs1029188462
NM_001105206.3(LAMA4):c.952A>G (p.Ile318Val) rs141372605
NM_001105206.3(LAMA4):c.962T>C (p.Leu321Pro) rs1554347065
NM_001105206.3(LAMA4):c.964A>C (p.Lys322Gln) rs1375382054
NM_001105206.3(LAMA4):c.98C>G (p.Pro33Arg) rs782047461
NM_001105206.3(LAMA4):c.997G>A (p.Ala333Thr) rs576711704

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