ClinVar Miner

List of variants in gene LAMA4 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.3283-15C>T rs2032568 0.77184
NM_001105206.3(LAMA4):c.3349G>A (p.Gly1117Ser) rs2032567 0.77036
NM_001105206.3(LAMA4):c.1492T>C (p.Tyr498His) rs1050348 0.66129
NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=) rs1050353 0.29327
NM_001105206.3(LAMA4):c.651C>T (p.Thr217=) rs2072021 0.26664
NM_001105206.3(LAMA4):c.5326+6T>G rs3734289 0.24973
NM_001105206.3(LAMA4):c.5326+15A>C rs3734290 0.24942
NM_001105206.3(LAMA4):c.3356C>G (p.Pro1119Arg) rs1050349 0.21500
NM_001105206.3(LAMA4):c.1710T>C (p.Ser570=) rs3752577 0.08618
NM_001105206.3(LAMA4):c.1357+4G>T rs6917763 0.07821
NM_001105206.3(LAMA4):c.4716C>T (p.Leu1572=) rs35679345 0.06874
NM_001105206.3(LAMA4):c.460C>T (p.Arg154Trp) rs11757455 0.04245
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515 0.03405
NM_001105206.3(LAMA4):c.195+144T>C rs147118520 0.01345
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902 0.01045
NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr) rs144482486 0.00228
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603 0.00205
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488 0.00091
NM_001105206.3(LAMA4):c.2403G>A (p.Thr801=) rs142559688 0.00078
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819 0.00078
NM_001105206.3(LAMA4):c.297+8G>A rs200595773 0.00075
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.5344C>T (p.Arg1782Cys) rs145897390 0.00046
NM_001105206.3(LAMA4):c.863C>G (p.Ala288Gly) rs150084275 0.00039
NM_001105206.3(LAMA4):c.141G>A (p.Pro47=) rs141926228 0.00035
NM_001105206.3(LAMA4):c.4436G>A (p.Arg1479His) rs140346737 0.00028
NM_001105206.3(LAMA4):c.1158G>A (p.Glu386=) rs147894075 0.00027
NM_001105206.3(LAMA4):c.4852C>T (p.Leu1618Phe) rs397516733 0.00020
NM_001105206.3(LAMA4):c.354C>T (p.Ile118=) rs144933976 0.00015
NM_001105206.3(LAMA4):c.3558-7T>C rs200864778 0.00014
NM_001105206.3(LAMA4):c.873C>T (p.Ile291=) rs141611768 0.00014
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.1551+4C>T rs201209516 0.00010
NM_001105206.3(LAMA4):c.3817T>C (p.Phe1273Leu) rs781966924 0.00009
NM_001105206.3(LAMA4):c.5442C>T (p.Ala1814=) rs200300118 0.00009
NM_001105206.3(LAMA4):c.1020C>T (p.Asn340=) rs147822567 0.00006
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342 0.00006
NM_001105206.3(LAMA4):c.3246A>G (p.Pro1082=) rs782387031 0.00004
NM_001105206.3(LAMA4):c.4171T>C (p.Tyr1391His) rs201094782 0.00004
NM_001105206.3(LAMA4):c.3559G>A (p.Ala1187Thr) rs781943786 0.00002
NM_001105206.3(LAMA4):c.2577G>A (p.Thr859=) rs397516724 0.00001
NM_001105206.3(LAMA4):c.2667C>T (p.Asn889=) rs112224872 0.00001
NM_001105206.3(LAMA4):c.4223C>T (p.Pro1408Leu) rs148968696 0.00001
NM_001105206.3(LAMA4):c.1194CAA[2] (p.Asn400del)
NM_001105206.3(LAMA4):c.1647A>C (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1669-7del rs531072297
NM_001105206.3(LAMA4):c.195+120C>G
NM_001105206.3(LAMA4):c.195+39T>A
NM_001105206.3(LAMA4):c.3166G>A (p.Gly1056Ser) rs145321940
NM_001105206.3(LAMA4):c.4066G>A (p.Gly1356Ser)
NM_001105206.3(LAMA4):c.4562C>T (p.Thr1521Ile)
NM_001105206.3(LAMA4):c.5067_5068del (p.His1689fs)
NM_001105206.3(LAMA4):c.605G>A (p.Cys202Tyr)
NM_001105206.3(LAMA4):c.730G>C (p.Gly244Arg) rs147078770
NM_001105206.3(LAMA4):c.859G>T (p.Ala287Ser) rs1782763341

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