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: 119
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HGVS dbSNP
NC_000006.12:g.112185360G>A
NM_001105206.3(LAMA4):c.*1C>T rs148811960
NM_001105206.3(LAMA4):c.-147C>T rs1554190701
NM_001105206.3(LAMA4):c.-37G>A rs1057524135
NM_001105206.3(LAMA4):c.1020C>T (p.Asn340=) rs147822567
NM_001105206.3(LAMA4):c.106A>G (p.Ile36Val) rs727503116
NM_001105206.3(LAMA4):c.1077+8dup rs397516713
NM_001105206.3(LAMA4):c.1140C>T (p.His380=) rs782378476
NM_001105206.3(LAMA4):c.1189+8T>C rs377133875
NM_001105206.3(LAMA4):c.1209C>T (p.Leu403=) rs397516715
NM_001105206.3(LAMA4):c.122C>T (p.Ala41Val) rs553474007
NM_001105206.3(LAMA4):c.1326C>T (p.Leu442=) rs3752580
NM_001105206.3(LAMA4):c.1353C>T (p.Tyr451=) rs782546070
NM_001105206.3(LAMA4):c.1357+15C>G rs782734095
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>A (p.Pro47=) rs141926228
NM_001105206.3(LAMA4):c.141G>T (p.Pro47=) rs141926228
NM_001105206.3(LAMA4):c.1551+4C>T rs201209516
NM_001105206.3(LAMA4):c.1613C>T (p.Ala538Val) rs782569832
NM_001105206.3(LAMA4):c.1614G>A (p.Ala538=) rs143587921
NM_001105206.3(LAMA4):c.1614G>T (p.Ala538=) rs143587921
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075
NM_001105206.3(LAMA4):c.1668+9G>A rs201457182
NM_001105206.3(LAMA4):c.1674G>A (p.Ala558=) rs150809897
NM_001105206.3(LAMA4):c.1716A>G (p.Leu572=) rs1057524660
NM_001105206.3(LAMA4):c.1719A>G (p.Gln573=) rs782237472
NM_001105206.3(LAMA4):c.1761C>T (p.Val587=) rs1554337616
NM_001105206.3(LAMA4):c.1818-16G>A rs1417950801
NM_001105206.3(LAMA4):c.196-11G>A rs374364713
NM_001105206.3(LAMA4):c.196-9C>T rs144850734
NM_001105206.3(LAMA4):c.1960-3T>C rs373682270
NM_001105206.3(LAMA4):c.1988T>C (p.Ile663Thr) rs538726706
NM_001105206.3(LAMA4):c.1999G>T (p.Asp667Tyr) rs397516720
NM_001105206.3(LAMA4):c.2056+12C>T rs397516722
NM_001105206.3(LAMA4):c.2090G>A (p.Arg697His) rs397516723
NM_001105206.3(LAMA4):c.225G>A (p.Leu75=) rs137948709
NM_001105206.3(LAMA4):c.228G>A (p.Ser76=) rs200589775
NM_001105206.3(LAMA4):c.2331A>C (p.Ala777=) rs1057524524
NM_001105206.3(LAMA4):c.2334G>A (p.Val778=) rs559504162
NM_001105206.3(LAMA4):c.2354-18A>T rs781939034
NM_001105206.3(LAMA4):c.2354-19T>C rs192622568
NM_001105206.3(LAMA4):c.2403G>A (p.Thr801=) rs142559688
NM_001105206.3(LAMA4):c.2493+15G>T rs77901141
NM_001105206.3(LAMA4):c.2494-13T>C rs576422943
NM_001105206.3(LAMA4):c.2569G>A (p.Ala857Thr) rs144123257
NM_001105206.3(LAMA4):c.2577G>A (p.Thr859=) rs397516724
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073
NM_001105206.3(LAMA4):c.2667C>T (p.Asn889=) rs112224872
NM_001105206.3(LAMA4):c.267C>T (p.Asn89=) rs727503114
NM_001105206.3(LAMA4):c.2734A>T (p.Thr912Ser) rs863223684
NM_001105206.3(LAMA4):c.279C>T (p.Asp93=) rs397516726
NM_001105206.3(LAMA4):c.2810A>G (p.Glu937Gly) rs35605307
NM_001105206.3(LAMA4):c.2850G>A (p.Pro950=) rs368741631
NM_001105206.3(LAMA4):c.2940A>C (p.Thr980=) rs397516727
NM_001105206.3(LAMA4):c.2950G>A (p.Val984Ile) rs145648026
NM_001105206.3(LAMA4):c.297+8G>A rs200595773
NM_001105206.3(LAMA4):c.2977-5C>T rs1554332652
NM_001105206.3(LAMA4):c.3003C>T (p.Gly1001=) rs397516728
NM_001105206.3(LAMA4):c.3087C>T (p.Pro1029=) rs146880158
NM_001105206.3(LAMA4):c.3111-18G>A rs80168443
NM_001105206.3(LAMA4):c.3111-18G>T rs80168443
NM_001105206.3(LAMA4):c.3246A>G (p.Pro1082=) rs782387031
NM_001105206.3(LAMA4):c.3282+7A>C rs782506211
NM_001105206.3(LAMA4):c.3311A>G (p.Asn1104Ser) rs542157463
NM_001105206.3(LAMA4):c.3357T>G (p.Pro1119=) rs782316528
NM_001105206.3(LAMA4):c.3375G>A (p.Thr1125=) rs143728627
NM_001105206.3(LAMA4):c.3414+7A>C rs992517796
NM_001105206.3(LAMA4):c.3415-7C>G rs1554330943
NM_001105206.3(LAMA4):c.343G>A (p.Asp115Asn) rs781919095
NM_001105206.3(LAMA4):c.3561C>T (p.Ala1187=) rs782306969
NM_001105206.3(LAMA4):c.3684A>G (p.Pro1228=) rs144541357
NM_001105206.3(LAMA4):c.3696+8C>T rs782714768
NM_001105206.3(LAMA4):c.3819C>T (p.Phe1273=) rs138232283
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.3897A>G (p.Lys1299=) rs876657482
NM_001105206.3(LAMA4):c.392C>T (p.Pro131Leu) rs374273620
NM_001105206.3(LAMA4):c.3933G>A (p.Leu1311=) rs1554329558
NM_001105206.3(LAMA4):c.412C>T (p.His138Tyr) rs727503113
NM_001105206.3(LAMA4):c.4305T>C (p.Asp1435=) rs147800037
NM_001105206.3(LAMA4):c.4386C>T (p.Ser1462=) rs397516729
NM_001105206.3(LAMA4):c.4475+14C>T rs782489593
NM_001105206.3(LAMA4):c.456T>A (p.Ala152=) rs149106800
NM_001105206.3(LAMA4):c.4626T>C (p.Ile1542=) rs150791451
NM_001105206.3(LAMA4):c.465C>T (p.Cys155=) rs150354594
NM_001105206.3(LAMA4):c.4665+15G>A rs377415750
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819
NM_001105206.3(LAMA4):c.4691G>T (p.Ser1564Ile) rs369887291
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048
NM_001105206.3(LAMA4):c.4839T>C (p.Ser1613=) rs782331970
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734
NM_001105206.3(LAMA4):c.4981+9A>G rs1057524450
NM_001105206.3(LAMA4):c.5002T>C (p.Leu1668=) rs369799390
NM_001105206.3(LAMA4):c.5046C>T (p.Ser1682=) rs782783070
NM_001105206.3(LAMA4):c.5113-16G>A rs371620356
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488
NM_001105206.3(LAMA4):c.5207-14G>C rs112265545
NM_001105206.3(LAMA4):c.5241G>A (p.Val1747=) rs375447272
NM_001105206.3(LAMA4):c.5400A>G (p.Gly1800=) rs782106622
NM_001105206.3(LAMA4):c.5442C>T (p.Ala1814=) rs200300118
NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr) rs144482486
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_001105206.3(LAMA4):c.668G>A (p.Arg223His) rs200017155
NM_001105206.3(LAMA4):c.66C>T (p.Ser22=) rs782600342
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862
NM_001105206.3(LAMA4):c.730G>C (p.Gly244Arg) rs147078770
NM_001105206.3(LAMA4):c.753A>C (p.Val251=) rs782296410
NM_001105206.3(LAMA4):c.828C>T (p.Cys276=) rs782380339
NM_001105206.3(LAMA4):c.85G>A (p.Asp29Asn) rs150662822
NM_001105206.3(LAMA4):c.85G>C (p.Asp29His) rs150662822
NM_001105206.3(LAMA4):c.863C>G (p.Ala288Gly) rs150084275
NM_001105206.3(LAMA4):c.873C>T (p.Ile291=) rs141611768
NM_001105206.3(LAMA4):c.90C>T (p.Asn30=) rs542554847
NM_001105206.3(LAMA4):c.945C>T (p.Asn315=) rs782772720
NM_001105206.3(LAMA4):c.996C>T (p.Tyr332=) rs188272639
NM_001105206.3(LAMA4):c.997G>A (p.Ala333Thr) rs576711704
NM_002290.4(LAMA4):c.1648-7delT rs531072297

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