ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance for not specified

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.195+131C>G rs138579810 0.00210
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579 0.00093
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044 0.00074
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519 0.00067
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811 0.00064
NM_001105206.3(LAMA4):c.196-15G>C rs371906362 0.00060
NM_001105206.3(LAMA4):c.5344C>T (p.Arg1782Cys) rs145897390 0.00046
NM_001105206.3(LAMA4):c.254A>G (p.Asn85Ser) rs145301300 0.00043
NM_001105206.3(LAMA4):c.967-15C>G rs375041786 0.00043
NM_001105206.3(LAMA4):c.863C>G (p.Ala288Gly) rs150084275 0.00039
NM_001105206.3(LAMA4):c.4436G>A (p.Arg1479His) rs140346737 0.00028
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442 0.00022
NM_001105206.3(LAMA4):c.4852C>T (p.Leu1618Phe) rs397516733 0.00020
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093 0.00016
NM_001105206.3(LAMA4):c.1298G>A (p.Arg433His) rs369658574 0.00015
NM_001105206.3(LAMA4):c.4792G>T (p.Ala1598Ser) rs202176359 0.00015
NM_001105206.3(LAMA4):c.3558-7T>C rs200864778 0.00014
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207 0.00013
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320 0.00012
NM_001105206.3(LAMA4):c.5270C>T (p.Pro1757Leu) rs200177134 0.00012
NM_001105206.3(LAMA4):c.1390C>G (p.His464Asp) rs151119304 0.00010
NM_001105206.3(LAMA4):c.1551+4C>T rs201209516 0.00010
NM_001105206.3(LAMA4):c.4405G>A (p.Ala1469Thr) rs727504595 0.00008
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342 0.00006
NM_001105206.3(LAMA4):c.4168C>T (p.Arg1390Trp) rs200189282 0.00006
NM_001105206.3(LAMA4):c.4679G>A (p.Arg1560Gln) rs397516732 0.00006
NM_001105206.3(LAMA4):c.5444dup (p.Ser1816fs) rs782327744 0.00006
NM_001105206.3(LAMA4):c.5380C>T (p.Arg1794Cys) rs781802725 0.00005
NM_001105206.3(LAMA4):c.1503T>A (p.Asp501Glu) rs370194991 0.00004
NM_001105206.3(LAMA4):c.1358-12A>G rs397516716 0.00003
NM_001105206.3(LAMA4):c.2225A>G (p.Asn742Ser) rs374279330 0.00002
NM_001105206.3(LAMA4):c.1078-14C>T rs397516714 0.00001
NM_001105206.3(LAMA4):c.153C>A (p.Ser51Arg) rs782192817 0.00001
NM_001105206.3(LAMA4):c.1643T>C (p.Leu548Pro) rs1562683086 0.00001
NM_001105206.3(LAMA4):c.1867G>A (p.Ala623Thr) rs782574915 0.00001
NM_001105206.3(LAMA4):c.2026G>A (p.Ala676Thr) rs397516721 0.00001
NM_001105206.3(LAMA4):c.2215G>A (p.Glu739Lys) rs727504935 0.00001
NM_001105206.3(LAMA4):c.398C>G (p.Pro133Arg) rs876657842 0.00001
NM_001105206.3(LAMA4):c.4052A>G (p.Lys1351Arg) rs876657843 0.00001
NM_001105206.3(LAMA4):c.4476-3C>A rs397516731 0.00001
NM_001105206.3(LAMA4):c.4476-4C>A rs727505042 0.00001
NM_001105206.3(LAMA4):c.4708G>T (p.Asp1570Tyr) rs199938033 0.00001
NM_001105206.3(LAMA4):c.4982-3del rs727505356 0.00001
NM_001105206.3(LAMA4):c.1077+13G>C
NM_001105206.3(LAMA4):c.1083T>A (p.Asn361Lys) rs1057518612
NM_001105206.3(LAMA4):c.1551+5A>G rs1554342189
NM_001105206.3(LAMA4):c.1598C>A (p.Ser533Tyr) rs782202196
NM_001105206.3(LAMA4):c.1922C>G (p.Ala641Gly) rs397516718
NM_001105206.3(LAMA4):c.195+4_195+5del rs397516719
NM_001105206.3(LAMA4):c.2640G>T (p.Gln880His) rs397516725
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.4446T>G (p.Phe1482Leu) rs397516730
NM_001105206.3(LAMA4):c.4455A>C (p.Leu1485Phe) rs1554326282
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.5066A>T (p.His1689Leu)
NM_001105206.3(LAMA4):c.5267G>A (p.Gly1756Glu) rs782244308

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