ClinVar Miner

List of variants in gene LAMA4 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 136
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HGVS dbSNP
NC_000006.12:g.112150420_112150423del
NC_000006.12:g.112154657del
NC_000006.12:g.112158541_112158544del
NC_000006.12:g.112159133del
NM_001105206.3(LAMA4):c.1035G>A (p.Thr345=) rs147069572
NM_001105206.3(LAMA4):c.1077+64C>T
NM_001105206.3(LAMA4):c.1078-195T>A
NM_001105206.3(LAMA4):c.1078-201A>T
NM_001105206.3(LAMA4):c.1078-222C>A
NM_001105206.3(LAMA4):c.1189+78C>T
NM_001105206.3(LAMA4):c.1190-165C>T
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515
NM_001105206.3(LAMA4):c.1357+4G>T rs6917763
NM_001105206.3(LAMA4):c.141G>A (p.Pro47=) rs141926228
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579
NM_001105206.3(LAMA4):c.1492T>C (p.Tyr498His) rs1050348
NM_001105206.3(LAMA4):c.1551+8G>A rs782128294
NM_001105206.3(LAMA4):c.1647A>C (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1669-286_1669-285del
NM_001105206.3(LAMA4):c.1710T>C (p.Ser570=) rs3752577
NM_001105206.3(LAMA4):c.1817+42G>A
NM_001105206.3(LAMA4):c.1818-231C>G
NM_001105206.3(LAMA4):c.1821G>A (p.Lys607=) rs374481199
NM_001105206.3(LAMA4):c.1854G>A (p.Gln618=) rs587781014
NM_001105206.3(LAMA4):c.195+144T>C rs147118520
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044
NM_001105206.3(LAMA4):c.196-12T>C rs78871662
NM_001105206.3(LAMA4):c.196-15G>C rs371906362
NM_001105206.3(LAMA4):c.196-191T>C
NM_001105206.3(LAMA4):c.196-304A>G
NM_001105206.3(LAMA4):c.196-9C>T rs144850734
NM_001105206.3(LAMA4):c.1960-61A>G
NM_001105206.3(LAMA4):c.2056+196G>A
NM_001105206.3(LAMA4):c.2056+40G>T
NM_001105206.3(LAMA4):c.2057-176T>C
NM_001105206.3(LAMA4):c.2173+251C>G
NM_001105206.3(LAMA4):c.2173+25C>G
NM_001105206.3(LAMA4):c.2174-180A>T
NM_001105206.3(LAMA4):c.2174-28A>C
NM_001105206.3(LAMA4):c.2250G>A (p.Gln750=) rs112305543
NM_001105206.3(LAMA4):c.228G>A (p.Ser76=) rs200589775
NM_001105206.3(LAMA4):c.2353+180A>G
NM_001105206.3(LAMA4):c.2354-323A>G
NM_001105206.3(LAMA4):c.2493+20A>T rs143397006
NM_001105206.3(LAMA4):c.2494-199C>T
NM_001105206.3(LAMA4):c.2494-209dup
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073
NM_001105206.3(LAMA4):c.2667+245A>G
NM_001105206.3(LAMA4):c.2668-177C>T
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917
NM_001105206.3(LAMA4):c.2810A>G (p.Glu937Gly) rs35605307
NM_001105206.3(LAMA4):c.297+72T>C
NM_001105206.3(LAMA4):c.298-104T>C
NM_001105206.3(LAMA4):c.298-135T>C
NM_001105206.3(LAMA4):c.298-179C>A
NM_001105206.3(LAMA4):c.298-213A>T
NM_001105206.3(LAMA4):c.298-247T>G
NM_001105206.3(LAMA4):c.298-267T>C
NM_001105206.3(LAMA4):c.3111-155C>T
NM_001105206.3(LAMA4):c.3111-48C>T
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902
NM_001105206.3(LAMA4):c.3283-15C>T rs2032568
NM_001105206.3(LAMA4):c.3349G>A (p.Gly1117Ser) rs2032567
NM_001105206.3(LAMA4):c.3356C>G (p.Pro1119Arg) rs1050349
NM_001105206.3(LAMA4):c.3414+169A>G
NM_001105206.3(LAMA4):c.3414+180T>A
NM_001105206.3(LAMA4):c.3415-316_3415-313del
NM_001105206.3(LAMA4):c.3696+109C>T
NM_001105206.3(LAMA4):c.3834+19C>G rs187178059
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342
NM_001105206.3(LAMA4):c.3835-258C>T
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811
NM_001105206.3(LAMA4):c.4065C>T (p.Phe1355=) rs34753919
NM_001105206.3(LAMA4):c.4134-243A>G
NM_001105206.3(LAMA4):c.4134-74C>G
NM_001105206.3(LAMA4):c.4173T>C (p.Tyr1391=) rs35042032
NM_001105206.3(LAMA4):c.422+20G>T rs188820838
NM_001105206.3(LAMA4):c.422+210G>C
NM_001105206.3(LAMA4):c.422+312C>T
NM_001105206.3(LAMA4):c.422+313A>G
NM_001105206.3(LAMA4):c.423-10C>T rs75058449
NM_001105206.3(LAMA4):c.423-202C>T
NM_001105206.3(LAMA4):c.423-4T>G rs79008328
NM_001105206.3(LAMA4):c.4287+15C>T rs116361180
NM_001105206.3(LAMA4):c.4287+211G>A
NM_001105206.3(LAMA4):c.4314A>C (p.Ser1438=) rs77367833
NM_001105206.3(LAMA4):c.4475+125C>T
NM_001105206.3(LAMA4):c.4475+83C>T
NM_001105206.3(LAMA4):c.4476-153T>C
NM_001105206.3(LAMA4):c.4476-80del
NM_001105206.3(LAMA4):c.456T>A (p.Ala152=) rs149106800
NM_001105206.3(LAMA4):c.460C>T (p.Arg154Trp) rs11757455
NM_001105206.3(LAMA4):c.4646A>G (p.Asn1549Ser) rs12110554
NM_001105206.3(LAMA4):c.4665+15G>A rs377415750
NM_001105206.3(LAMA4):c.4665+8G>T rs184220860
NM_001105206.3(LAMA4):c.4666-277G>A
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819
NM_001105206.3(LAMA4):c.4716C>T (p.Leu1572=) rs35679345
NM_001105206.3(LAMA4):c.4821+160C>A
NM_001105206.3(LAMA4):c.4821+219C>G
NM_001105206.3(LAMA4):c.4821+245A>G
NM_001105206.3(LAMA4):c.4822-156G>C
NM_001105206.3(LAMA4):c.4981+29del
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180
NM_001105206.3(LAMA4):c.503+93G>T
NM_001105206.3(LAMA4):c.5112+245C>T
NM_001105206.3(LAMA4):c.5113-111_5113-110del
NM_001105206.3(LAMA4):c.5113-166G>A
NM_001105206.3(LAMA4):c.5113-239C>A
NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=) rs1050353
NM_001105206.3(LAMA4):c.5206+184C>T
NM_001105206.3(LAMA4):c.5206+59C>A
NM_001105206.3(LAMA4):c.5206+70C>G
NM_001105206.3(LAMA4):c.5207-14G>C rs112265545
NM_001105206.3(LAMA4):c.5207-49_5207-47dup
NM_001105206.3(LAMA4):c.531C>T (p.Pro177=) rs61742228
NM_001105206.3(LAMA4):c.5326+15A>C rs3734290
NM_001105206.3(LAMA4):c.5326+6T>G rs3734289
NM_001105206.3(LAMA4):c.5327-101A>G
NM_001105206.3(LAMA4):c.5340A>G (p.Thr1780=) rs139241892
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292
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.651C>T (p.Thr217=) rs2072021
NM_001105206.3(LAMA4):c.815-36T>C
NM_001105206.3(LAMA4):c.848= (p.Asp283=) rs879974322
NM_001105206.3(LAMA4):c.848_849= (p.Asp283=) rs71543223
NM_001105206.3(LAMA4):c.849= (p.Asp283=) rs9387061
NM_001105206.3(LAMA4):c.888C>T (p.Ser296=) rs17073495
NM_001105206.3(LAMA4):c.921T>G (p.Ala307=) rs186498011
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603
NM_001105206.3(LAMA4):c.966+135A>G
NM_001105206.3(LAMA4):c.966+144A>T
NM_001105206.3(LAMA4):c.966+78C>G
NM_001105206.3(LAMA4):c.967-34C>A

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