ClinVar Miner

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

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Total variants: 63
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HGVS dbSNP
NM_001105206.2(LAMA4):c.196-12T>C rs78871662
NM_001105206.2(LAMA4):c.4287+15C>T rs116361180
NM_001105206.2(LAMA4):c.5207-14G>C rs112265545
NM_002290.4(LAMA4):c.1014G>A (p.Thr338=) rs147069572
NM_002290.4(LAMA4):c.1169-8C>G rs73538515
NM_002290.4(LAMA4):c.1305C>T (p.Leu435=) rs3752580
NM_002290.4(LAMA4):c.1336+4G>T rs6917763
NM_002290.4(LAMA4):c.1454T>A (p.Leu485His) rs3752579
NM_002290.4(LAMA4):c.1471T>C (p.Tyr491His) rs1050348
NM_002290.4(LAMA4):c.1530+8G>A rs782128294
NM_002290.4(LAMA4):c.1626A>C (p.Ser542=) rs149459643
NM_002290.4(LAMA4):c.1689T>C (p.Ser563=) rs3752577
NM_002290.4(LAMA4):c.1800G>A (p.Lys600=) rs374481199
NM_002290.4(LAMA4):c.1833G>A (p.Gln611=) rs587781014
NM_002290.4(LAMA4):c.1938T>C (p.Asp646=) rs143269044
NM_002290.4(LAMA4):c.196-15G>C rs371906362
NM_002290.4(LAMA4):c.196-9C>T rs144850734
NM_002290.4(LAMA4):c.2229G>A (p.Gln743=) rs112305543
NM_002290.4(LAMA4):c.228G>A (p.Ser76=) rs200589775
NM_002290.4(LAMA4):c.2472+15G>T rs77901141
NM_002290.4(LAMA4):c.2472+20A>T rs143397006
NM_002290.4(LAMA4):c.2634C>T (p.Leu878=) rs35772073
NM_002290.4(LAMA4):c.2789A>G (p.Glu930Gly) rs35605307
NM_002290.4(LAMA4):c.280G>A (p.Gly94Ser) rs35349917
NM_002290.4(LAMA4):c.297+2368G>A rs75992359
NM_002290.4(LAMA4):c.297+8G>A rs200595773
NM_002290.4(LAMA4):c.3154G>A (p.Val1052Met) rs373650093
NM_002290.4(LAMA4):c.3218G>A (p.Arg1073Gln) rs41289902
NM_002290.4(LAMA4):c.3262-15C>T rs2032568
NM_002290.4(LAMA4):c.3328G>A (p.Gly1110Ser) rs2032567
NM_002290.4(LAMA4):c.3335C>G (p.Pro1112Arg) rs1050349
NM_002290.4(LAMA4):c.3813+19C>G rs187178059
NM_002290.4(LAMA4):c.3813G>A (p.Gly1271=) rs141988342
NM_002290.4(LAMA4):c.3922G>A (p.Val1308Ile) rs70940811
NM_002290.4(LAMA4):c.4044C>T (p.Phe1348=) rs34753919
NM_002290.4(LAMA4):c.4152T>C (p.Tyr1384=) rs35042032
NM_002290.4(LAMA4):c.422+20G>T rs188820838
NM_002290.4(LAMA4):c.423-10C>T rs75058449
NM_002290.4(LAMA4):c.423-4T>G rs79008328
NM_002290.4(LAMA4):c.4293A>C (p.Ser1431=) rs77367833
NM_002290.4(LAMA4):c.456T>A (p.Ala152=) rs149106800
NM_002290.4(LAMA4):c.460C>T (p.Arg154Trp) rs11757455
NM_002290.4(LAMA4):c.4625A>G (p.Asn1542Ser) rs12110554
NM_002290.4(LAMA4):c.4644+15G>A rs377415750
NM_002290.4(LAMA4):c.4644+8G>T rs184220860
NM_002290.4(LAMA4):c.4657C>A (p.Arg1553=) rs150069819
NM_002290.4(LAMA4):c.4695C>T (p.Leu1565=) rs35679345
NM_002290.4(LAMA4):c.4995T>A (p.Ile1665=) rs148517180
NM_002290.4(LAMA4):c.5139T>A (p.Val1713=) rs1050353
NM_002290.4(LAMA4):c.5305+15A>C rs3734290
NM_002290.4(LAMA4):c.5305+6T>G rs3734289
NM_002290.4(LAMA4):c.5319A>G (p.Thr1773=) rs139241892
NM_002290.4(LAMA4):c.531C>T (p.Pro177=) rs61742228
NM_002290.4(LAMA4):c.5422G>A (p.Val1808Ile) rs3734292
NM_002290.4(LAMA4):c.5429T>C (p.Ile1810Thr) rs144482486
NM_002290.4(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_002290.4(LAMA4):c.651C>T (p.Thr217=) rs2072021
NM_002290.4(LAMA4):c.827A= (p.Asp276=) rs879974322
NM_002290.4(LAMA4):c.827_828AC= (p.Asp276=) rs71543223
NM_002290.4(LAMA4):c.828C= (p.Asp276=) rs9387061
NM_002290.4(LAMA4):c.867C>T (p.Ser289=) rs17073495
NM_002290.4(LAMA4):c.900T>G (p.Ala300=) rs186498011
NM_002290.4(LAMA4):c.903T>C (p.His301=) rs143580603

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