ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 50
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1078-14C>T rs397516714
NM_001105206.3(LAMA4):c.1298G>A (p.Arg433His) rs369658574
NM_001105206.3(LAMA4):c.1358-12A>G rs397516716
NM_001105206.3(LAMA4):c.1390C>G (p.His464Asp) rs151119304
NM_001105206.3(LAMA4):c.1503T>A (p.Asp501Glu) rs370194991
NM_001105206.3(LAMA4):c.1551+4C>T rs201209516
NM_001105206.3(LAMA4):c.1551+5A>G rs1554342189
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207
NM_001105206.3(LAMA4):c.1922C>G (p.Ala641Gly) rs397516718
NM_001105206.3(LAMA4):c.195+131C>G rs138579810
NM_001105206.3(LAMA4):c.195+4_195+5del rs397516719
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044
NM_001105206.3(LAMA4):c.196-15G>C rs371906362
NM_001105206.3(LAMA4):c.2026G>A (p.Ala676Thr) rs397516721
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2215G>A (p.Glu739Lys) rs727504935
NM_001105206.3(LAMA4):c.2225A>G (p.Asn742Ser) rs374279330
NM_001105206.3(LAMA4):c.254A>G (p.Asn85Ser) rs145301300
NM_001105206.3(LAMA4):c.2640G>T (p.Gln880His) rs397516725
NM_001105206.3(LAMA4):c.2758G>A (p.Asp920Asn) rs727503112
NM_001105206.3(LAMA4):c.2782C>A (p.Pro928Thr) rs727505130
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093
NM_001105206.3(LAMA4):c.3434A>G (p.Asn1145Ser) rs377528058
NM_001105206.3(LAMA4):c.3515A>G (p.Asp1172Gly) rs1554330855
NM_001105206.3(LAMA4):c.3558-7T>C rs200864778
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811
NM_001105206.3(LAMA4):c.398C>G (p.Pro133Arg) rs876657842
NM_001105206.3(LAMA4):c.4052A>G (p.Lys1351Arg) rs876657843
NM_001105206.3(LAMA4):c.4168C>T (p.Arg1390Trp) rs200189282
NM_001105206.3(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595
NM_001105206.3(LAMA4):c.4436G>A (p.Arg1479His) rs140346737
NM_001105206.3(LAMA4):c.4446T>G (p.Phe1482Leu) rs397516730
NM_001105206.3(LAMA4):c.4455A>C (p.Leu1485Phe) rs1554326282
NM_001105206.3(LAMA4):c.4476-3C>A rs397516731
NM_001105206.3(LAMA4):c.4476-4C>A rs727505042
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442
NM_001105206.3(LAMA4):c.4679G>A (p.Arg1560Gln) rs397516732
NM_001105206.3(LAMA4):c.4683_4684del (p.Arg1562fs) rs1554325284
NM_001105206.3(LAMA4):c.4696C>T (p.Arg1566Ter) rs1554325261
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.4982-3del rs727505356
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320
NM_001105206.3(LAMA4):c.5267G>A (p.Gly1756Glu) rs782244308
NM_001105206.3(LAMA4):c.5270C>T (p.Pro1757Leu) rs200177134
NM_001105206.3(LAMA4):c.5344C>T (p.Arg1782Cys) rs145897390
NM_001105206.3(LAMA4):c.5380C>T (p.Arg1794Cys) rs781802725
NM_001105206.3(LAMA4):c.863C>G (p.Ala288Gly) rs150084275
NM_001105206.3(LAMA4):c.967-15C>G rs375041786

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