ClinVar Miner

List of variants in gene LAMA4 reported as likely benign for not specified

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Gene type:
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Total variants: 117
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.3356C>G (p.Pro1119Arg) rs1050349 0.21500
NM_001105206.3(LAMA4):c.460C>T (p.Arg154Trp) rs11757455 0.04245
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917 0.01717
NM_001105206.3(LAMA4):c.4646A>G (p.Asn1549Ser) rs12110554 0.01544
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.5207-14G>C rs112265545 0.00214
NM_001105206.3(LAMA4):c.196-9C>T rs144850734 0.00174
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292 0.00174
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048 0.00151
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075 0.00135
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.2950G>A (p.Val984Ile) rs145648026 0.00072
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519 0.00067
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862 0.00052
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073 0.00051
NM_001105206.3(LAMA4):c.1668+9G>A rs201457182 0.00049
NM_001105206.3(LAMA4):c.4665+15G>A rs377415750 0.00049
NM_001105206.3(LAMA4):c.5344C>T (p.Arg1782Cys) rs145897390 0.00046
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419 0.00044
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.4626T>C (p.Ile1542=) rs150791451 0.00031
NM_001105206.3(LAMA4):c.1614G>A (p.Ala538=) rs143587921 0.00027
NM_001105206.3(LAMA4):c.456T>A (p.Ala152=) rs149106800 0.00022
NM_001105206.3(LAMA4):c.4691G>T (p.Ser1564Ile) rs369887291 0.00018
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093 0.00016
NM_001105206.3(LAMA4):c.3087C>T (p.Pro1029=) rs146880158 0.00015
NM_001105206.3(LAMA4):c.1674G>A (p.Ala558=) rs150809897 0.00014
NM_001105206.3(LAMA4):c.873C>T (p.Ile291=) rs141611768 0.00014
NM_001105206.3(LAMA4):c.1999G>T (p.Asp667Tyr) rs397516720 0.00011
NM_001105206.3(LAMA4):c.3819C>T (p.Phe1273=) rs138232283 0.00010
NM_001105206.3(LAMA4):c.5442C>T (p.Ala1814=) rs200300118 0.00009
NM_001105206.3(LAMA4):c.4305T>C (p.Asp1435=) rs147800037 0.00008
NM_001105206.3(LAMA4):c.1077+8dup rs397516713 0.00007
NM_001105206.3(LAMA4):c.2090G>A (p.Arg697His) rs397516723 0.00007
NM_001105206.3(LAMA4):c.1020C>T (p.Asn340=) rs147822567 0.00006
NM_001105206.3(LAMA4):c.1189+8T>C rs377133875 0.00006
NM_001105206.3(LAMA4):c.122C>T (p.Ala41Val) rs553474007 0.00006
NM_001105206.3(LAMA4):c.1353C>T (p.Tyr451=) rs782546070 0.00006
NM_001105206.3(LAMA4):c.1960-3T>C rs373682270 0.00006
NM_001105206.3(LAMA4):c.228G>A (p.Ser76=) rs200589775 0.00006
NM_001105206.3(LAMA4):c.2569G>A (p.Ala857Thr) rs144123257 0.00006
NM_001105206.3(LAMA4):c.279C>T (p.Asp93=) rs397516726 0.00006
NM_001105206.3(LAMA4):c.2940A>C (p.Thr980=) rs397516727 0.00006
NM_001105206.3(LAMA4):c.3897A>G (p.Lys1299=) rs876657482 0.00006
NM_001105206.3(LAMA4):c.5393T>C (p.Ile1798Thr) rs377204776 0.00006
NM_001105206.3(LAMA4):c.967-13C>T rs782148493 0.00006
NM_001105206.3(LAMA4):c.2354-18A>T rs781939034 0.00005
NM_001105206.3(LAMA4):c.5364C>A (p.Pro1788=) rs370510960 0.00005
NM_001105206.3(LAMA4):c.1357+15C>G rs782734095 0.00004
NM_001105206.3(LAMA4):c.2056+12C>T rs397516722 0.00004
NM_001105206.3(LAMA4):c.3246A>G (p.Pro1082=) rs782387031 0.00004
NM_001105206.3(LAMA4):c.412C>T (p.His138Tyr) rs727503113 0.00004
NM_001105206.3(LAMA4):c.1444A>G (p.Asn482Asp) rs782319667 0.00003
NM_001105206.3(LAMA4):c.3696+8C>T rs782714768 0.00003
NM_001105206.3(LAMA4):c.4475+14C>T rs782489593 0.00003
NM_001105206.3(LAMA4):c.945C>T (p.Asn315=) rs782772720 0.00003
NM_001105206.3(LAMA4):c.996C>T (p.Tyr332=) rs188272639 0.00003
NM_001105206.3(LAMA4):c.997G>A (p.Ala333Thr) rs576711704 0.00003
NM_001105206.3(LAMA4):c.1988T>C (p.Ile663Thr) rs538726706 0.00002
NM_001105206.3(LAMA4):c.2494-13T>C rs576422943 0.00002
NM_001105206.3(LAMA4):c.3357T>G (p.Pro1119=) rs782316528 0.00002
NM_001105206.3(LAMA4):c.3375G>A (p.Thr1125=) rs143728627 0.00002
NM_001105206.3(LAMA4):c.392C>T (p.Pro131Leu) rs374273620 0.00002
NM_001105206.3(LAMA4):c.465C>T (p.Cys155=) rs150354594 0.00002
NM_001105206.3(LAMA4):c.-37G>A rs1057524135 0.00001
NM_001105206.3(LAMA4):c.1209C>T (p.Leu403=) rs397516715 0.00001
NM_001105206.3(LAMA4):c.1719A>G (p.Gln573=) rs782237472 0.00001
NM_001105206.3(LAMA4):c.1818-16G>A rs1417950801 0.00001
NM_001105206.3(LAMA4):c.2354-19T>C rs192622568 0.00001
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.267C>T (p.Asn89=) rs727503114 0.00001
NM_001105206.3(LAMA4):c.3003C>T (p.Gly1001=) rs397516728 0.00001
NM_001105206.3(LAMA4):c.3414+7A>C rs992517796 0.00001
NM_001105206.3(LAMA4):c.343G>A (p.Asp115Asn) rs781919095 0.00001
NM_001105206.3(LAMA4):c.3561C>T (p.Ala1187=) rs782306969 0.00001
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734 0.00001
NM_001105206.3(LAMA4):c.5046C>T (p.Ser1682=) rs782783070 0.00001
NM_001105206.3(LAMA4):c.5113-16G>A rs371620356 0.00001
NM_001105206.3(LAMA4):c.5241G>A (p.Val1747=) rs375447272 0.00001
NM_001105206.3(LAMA4):c.753A>C (p.Val251=) rs782296410 0.00001
NM_001105206.3(LAMA4):c.90C>T (p.Asn30=) rs542554847 0.00001
NM_001105206.3(LAMA4):c.-147C>T rs1554190701
NM_001105206.3(LAMA4):c.106A>G (p.Ile36Val) rs727503116
NM_001105206.3(LAMA4):c.1140C>T (p.His380=) rs782378476
NM_001105206.3(LAMA4):c.1374G>A (p.Glu458=) rs397516717
NM_001105206.3(LAMA4):c.140C>T (p.Pro47Leu) rs727503115
NM_001105206.3(LAMA4):c.141G>T (p.Pro47=) rs141926228
NM_001105206.3(LAMA4):c.1614G>T (p.Ala538=) rs143587921
NM_001105206.3(LAMA4):c.1716A>G (p.Leu572=) rs1057524660
NM_001105206.3(LAMA4):c.1761C>T (p.Val587=) rs1554337616
NM_001105206.3(LAMA4):c.1779T>C (p.His593=)
NM_001105206.3(LAMA4):c.2331A>C (p.Ala777=) rs1057524524
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2977-5C>T rs1554332652
NM_001105206.3(LAMA4):c.3111-18G>A rs80168443
NM_001105206.3(LAMA4):c.3111-18G>T rs80168443
NM_001105206.3(LAMA4):c.3282+7A>C rs782506211
NM_001105206.3(LAMA4):c.3415-7C>G rs1554330943
NM_001105206.3(LAMA4):c.381A>G (p.Gln127=) rs782751372
NM_001105206.3(LAMA4):c.3846C>T (p.Phe1282=) rs1057523170
NM_001105206.3(LAMA4):c.3933G>A (p.Leu1311=) rs1554329558
NM_001105206.3(LAMA4):c.4170G>A (p.Arg1390=)
NM_001105206.3(LAMA4):c.4386C>T (p.Ser1462=) rs397516729
NM_001105206.3(LAMA4):c.4967G>T (p.Gly1656Val) rs41289900
NM_001105206.3(LAMA4):c.4981+9A>G rs1057524450
NM_001105206.3(LAMA4):c.5002T>C (p.Leu1668=) rs369799390
NM_001105206.3(LAMA4):c.5113-11A>G
NM_001105206.3(LAMA4):c.5400A>G (p.Gly1800=) rs782106622
NM_001105206.3(LAMA4):c.66C>T (p.Ser22=) rs782600342
NM_001105206.3(LAMA4):c.85G>A (p.Asp29Asn) rs150662822
NM_001105206.3(LAMA4):c.85G>C (p.Asp29His) rs150662822

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