ClinVar Miner

List of variants in gene LAMA4 reported as likely benign by GeneDx

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Gene type:
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Total variants: 116
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HGVS dbSNP
NC_000006.12:g.112141152del
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+286C>T
NM_001105206.3(LAMA4):c.1140C>T (p.His380=) rs782378476
NM_001105206.3(LAMA4):c.1190-132C>T
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.1357+312T>A
NM_001105206.3(LAMA4):c.141G>T (p.Pro47=) rs141926228
NM_001105206.3(LAMA4):c.1551+279G>A
NM_001105206.3(LAMA4):c.1551+4C>T rs201209516
NM_001105206.3(LAMA4):c.1552-184A>G
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+155A>T
NM_001105206.3(LAMA4):c.1674G>A (p.Ala558=) rs150809897
NM_001105206.3(LAMA4):c.1677A>G (p.Ser559=)
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.1817+111G>A
NM_001105206.3(LAMA4):c.1818-16G>A rs1417950801
NM_001105206.3(LAMA4):c.196-11G>A rs374364713
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.2056+70G>A
NM_001105206.3(LAMA4):c.2057-129A>G
NM_001105206.3(LAMA4):c.2057-210T>C
NM_001105206.3(LAMA4):c.225G>A (p.Leu75=) rs137948709
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.2354-114dup
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+125del
NM_001105206.3(LAMA4):c.2493+15G>T rs77901141
NM_001105206.3(LAMA4):c.2493+214A>G
NM_001105206.3(LAMA4):c.2494-115A>G
NM_001105206.3(LAMA4):c.2494-13T>C rs576422943
NM_001105206.3(LAMA4):c.2667+118A>G
NM_001105206.3(LAMA4):c.2667C>T (p.Asn889=) rs112224872
NM_001105206.3(LAMA4):c.2668-153A>C
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.2813+70C>T
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+260T>C
NM_001105206.3(LAMA4):c.297+8G>A rs200595773
NM_001105206.3(LAMA4):c.2977-16T>A
NM_001105206.3(LAMA4):c.3110+116A>C
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.3414+7A>C rs992517796
NM_001105206.3(LAMA4):c.3415-7C>G rs1554330943
NM_001105206.3(LAMA4):c.3558-14A>C
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+13C>T
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.3933G>A (p.Leu1311=) rs1554329558
NM_001105206.3(LAMA4):c.3969-312T>A
NM_001105206.3(LAMA4):c.4475+114T>C
NM_001105206.3(LAMA4):c.4475+14C>T rs782489593
NM_001105206.3(LAMA4):c.4475+74G>T
NM_001105206.3(LAMA4):c.4691G>T (p.Ser1564Ile) rs369887291
NM_001105206.3(LAMA4):c.4821+37T>G
NM_001105206.3(LAMA4):c.4822-192A>G
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048
NM_001105206.3(LAMA4):c.4839T>C (p.Ser1613=) rs782331970
NM_001105206.3(LAMA4):c.4981+9A>G rs1057524450
NM_001105206.3(LAMA4):c.503+49C>A
NM_001105206.3(LAMA4):c.503+71C>G
NM_001105206.3(LAMA4):c.503+88A>C
NM_001105206.3(LAMA4):c.5046C>T (p.Ser1682=) rs782783070
NM_001105206.3(LAMA4):c.5113-137C>T
NM_001105206.3(LAMA4):c.5113-16G>A rs371620356
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488
NM_001105206.3(LAMA4):c.5327-178T>C
NM_001105206.3(LAMA4):c.5327-301C>A
NM_001105206.3(LAMA4):c.5400A>G (p.Gly1800=) rs782106622
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.815-13G>C
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.945C>T (p.Asn315=) rs782772720
NM_001105206.3(LAMA4):c.966+308C>T
NM_001105206.3(LAMA4):c.967-228C>A
NM_001105206.3(LAMA4):c.967-57A>G
NM_001105206.3(LAMA4):c.996C>T (p.Tyr332=) rs188272639
NM_002290.4(LAMA4):c.1648-7delT rs531072297

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