ClinVar Miner

List of variants in gene LAMA3 reported as likely benign

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Total variants: 124
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HGVS dbSNP
NM_000227.5(LAMA3):c.1038T>C (p.Asp346=) rs151037092
NM_000227.5(LAMA3):c.1096C>T (p.Arg366Cys) rs141645580
NM_000227.5(LAMA3):c.1097G>A (p.Arg366His) rs149809232
NM_000227.5(LAMA3):c.1114C>T (p.Arg372Trp) rs34381515
NM_000227.5(LAMA3):c.1173G>A (p.Gln391=) rs1599038560
NM_000227.5(LAMA3):c.1197C>T (p.Thr399=) rs543980622
NM_000227.5(LAMA3):c.1227T>C (p.Asn409=) rs1599043125
NM_000227.5(LAMA3):c.123C>T (p.Pro41=) rs905847075
NM_000227.5(LAMA3):c.1266C>T (p.Tyr422=) rs752860014
NM_000227.5(LAMA3):c.1449G>A (p.Leu483=) rs1599048277
NM_000227.5(LAMA3):c.1562C>T (p.Ser521Phe) rs199684626
NM_000227.5(LAMA3):c.1567T>G (p.Ser523Ala) rs34590975
NM_000227.5(LAMA3):c.1608C>T (p.His536=) rs769711853
NM_000227.5(LAMA3):c.1609G>A (p.Ala537Thr) rs146005577
NM_000227.5(LAMA3):c.1611G>A (p.Ala537=) rs369554046
NM_000227.5(LAMA3):c.1627C>T (p.Leu543=) rs1599051119
NM_000227.5(LAMA3):c.1639C>T (p.Leu547=) rs1348713944
NM_000227.5(LAMA3):c.1659C>T (p.Asn553=) rs185563091
NM_000227.5(LAMA3):c.1698C>T (p.Ala566=) rs199949401
NM_000227.5(LAMA3):c.1710C>T (p.Tyr570=) rs544976035
NM_000227.5(LAMA3):c.1788+10T>C rs1599053919
NM_000227.5(LAMA3):c.1806T>C (p.Asp602=) rs1172061860
NM_000227.5(LAMA3):c.1978C>G (p.Leu660Val) rs138591939
NM_000227.5(LAMA3):c.2009-36_2009-16del rs1555734493
NM_000227.5(LAMA3):c.2040G>A (p.Lys680=) rs199663037
NM_000227.5(LAMA3):c.222G>A (p.Arg74=) rs151202077
NM_000227.5(LAMA3):c.2334T>C (p.Val778=) rs930568261
NM_000227.5(LAMA3):c.2403G>A (p.Leu801=) rs1599077059
NM_000227.5(LAMA3):c.2483T>C (p.Met828Thr) rs150804730
NM_000227.5(LAMA3):c.2625G>A (p.Glu875=) rs751418316
NM_000227.5(LAMA3):c.2654+5A>G rs142723653
NM_000227.5(LAMA3):c.2654+7G>C rs749770794
NM_000227.5(LAMA3):c.2654+9C>G rs867212066
NM_000227.5(LAMA3):c.2793T>C (p.Val931=) rs1599084162
NM_000227.5(LAMA3):c.2896T>C (p.Tyr966His) rs377097479
NM_000227.5(LAMA3):c.2913A>G (p.Thr971=) rs145848988
NM_000227.5(LAMA3):c.293A>G (p.Gln98Arg) rs138168899
NM_000227.5(LAMA3):c.2940G>A (p.Glu980=) rs1599086175
NM_000227.5(LAMA3):c.3201C>T (p.Asn1067=) rs35737354
NM_000227.5(LAMA3):c.3237A>G (p.Lys1079=) rs1599104164
NM_000227.5(LAMA3):c.3242A>G (p.Gln1081Arg) rs147208526
NM_000227.5(LAMA3):c.3327A>C (p.Gly1109=) rs149789872
NM_000227.5(LAMA3):c.3453C>T (p.Cys1151=) rs1599121723
NM_000227.5(LAMA3):c.3516T>A (p.Thr1172=) rs1362535126
NM_000227.5(LAMA3):c.3609+8G>A rs776398819
NM_000227.5(LAMA3):c.3609+8G>C rs776398819
NM_000227.5(LAMA3):c.363C>T (p.Ser121=) rs145159456
NM_000227.5(LAMA3):c.3669C>T (p.Ser1223=) rs777874539
NM_000227.5(LAMA3):c.3699G>A (p.Thr1233=) rs546328935
NM_000227.5(LAMA3):c.3729T>C (p.Ser1243=) rs756235025
NM_000227.5(LAMA3):c.3750A>T (p.Gly1250=) rs140184530
NM_000227.5(LAMA3):c.3765C>T (p.Ile1255=) rs779758375
NM_000227.5(LAMA3):c.3909T>C (p.Asp1303=) rs1599135954
NM_000227.5(LAMA3):c.4152C>A (p.Pro1384=) rs539066696
NM_000227.5(LAMA3):c.4167A>C (p.Leu1389=) rs566439275
NM_000227.5(LAMA3):c.4263T>C (p.Thr1421=) rs1379162353
NM_000227.5(LAMA3):c.429C>T (p.Asp143=) rs201107968
NM_000227.5(LAMA3):c.4382C>T (p.Thr1461Met) rs117056996
NM_000227.5(LAMA3):c.4383+7G>C rs756197658
NM_000227.5(LAMA3):c.4384-21C>T rs2288592
NM_000227.5(LAMA3):c.4446G>A (p.Glu1482=) rs146163295
NM_000227.5(LAMA3):c.4485G>A (p.Ala1495=) rs759662848
NM_000227.5(LAMA3):c.4608C>T (p.Phe1536=) rs372697000
NM_000227.5(LAMA3):c.4609G>A (p.Gly1537Arg) rs78615698
NM_000227.5(LAMA3):c.4686T>C (p.Ala1562=) rs370241931
NM_000227.5(LAMA3):c.4695A>G (p.Val1565=) rs752284879
NM_000227.5(LAMA3):c.4696T>C (p.Leu1566=) rs538133914
NM_000227.5(LAMA3):c.4747A>T (p.Thr1583Ser) rs115991457
NM_000227.5(LAMA3):c.4822G>A (p.Ala1608Thr) rs141992173
NM_000227.5(LAMA3):c.4836T>C (p.Ser1612=) rs1599188677
NM_000227.5(LAMA3):c.4890A>G (p.Gly1630=) rs753060873
NM_000227.5(LAMA3):c.4902G>A (p.Ser1634=) rs141464226
NM_000227.5(LAMA3):c.5013C>T (p.His1671=) rs575174453
NM_000227.5(LAMA3):c.5023G>T (p.Ala1675Ser) rs563708367
NM_000227.5(LAMA3):c.513C>T (p.Phe171=) rs138524783
NM_000227.5(LAMA3):c.583+8C>T rs377137540
NM_000227.5(LAMA3):c.609T>C (p.Asp203=) rs775135907
NM_000227.5(LAMA3):c.635-10G>A rs750901851
NM_000227.5(LAMA3):c.744G>A (p.Leu248=) rs546675242
NM_000227.5(LAMA3):c.76C>A (p.Leu26Met) rs148634422
NM_000227.5(LAMA3):c.831A>G (p.Ser277=) rs780825151
NM_000227.5(LAMA3):c.960C>T (p.Ser320=) rs76309383
NM_000227.5(LAMA3):c.972G>A (p.Leu324=) rs370165389
NM_198129.3(LAMA3):c.4998+1533T>C rs770960237
NM_198129.3(LAMA3):c.5169T>C (p.Tyr1723=) rs140561492
NM_198129.3(LAMA3):c.5493C>T (p.Asn1831=) rs199982757
NM_198129.3(LAMA3):c.5522G>A (p.Arg1841His) rs144475991
NM_198129.3(LAMA3):c.7218C>T (p.Asp2406=) rs62093184
NM_198129.3(LAMA3):c.7482-5A>C rs780657629
NM_198129.3(LAMA3):c.7545C>T (p.Pro2515=) rs145460785
NM_198129.3(LAMA3):c.7727A>G (p.Asn2576Ser) rs781529313
NM_198129.3(LAMA3):c.7797C>T (p.Asp2599=) rs61751706
NM_198129.3(LAMA3):c.7928G>T (p.Arg2643Leu) rs45516998
NM_198129.3(LAMA3):c.8193G>C (p.Thr2731=) rs762861196
NM_198129.3(LAMA3):c.8241C>T (p.Val2747=) rs371174542
NM_198129.3(LAMA3):c.8282C>T (p.Ser2761Leu) rs144549206
NM_198129.3(LAMA3):c.8283G>A (p.Ser2761=) rs146634036
NM_198129.3(LAMA3):c.8576+7G>T rs1258107
NM_198129.3(LAMA3):c.8629C>T (p.His2877Tyr) rs35153125
NM_198129.3(LAMA3):c.9241C>T (p.Arg3081Cys) rs35762515
NM_198129.3(LAMA3):c.9559C>T (p.Arg3187Cys) rs150956802
NM_198129.4(LAMA3):c.1032C>T (p.Pro344=) rs774453548
NM_198129.4(LAMA3):c.1130G>A (p.Ser377Asn) rs370710933
NM_198129.4(LAMA3):c.1154C>A (p.Ala385Asp) rs772044341
NM_198129.4(LAMA3):c.1158T>C (p.Gly386=) rs200033487
NM_198129.4(LAMA3):c.1283G>C (p.Cys428Ser) rs180795245
NM_198129.4(LAMA3):c.1571G>A (p.Arg524His) rs201845068
NM_198129.4(LAMA3):c.1889-9T>C rs533251361
NM_198129.4(LAMA3):c.1989C>T (p.Cys663=) rs558629621
NM_198129.4(LAMA3):c.2205C>T (p.Asp735=) rs376350919
NM_198129.4(LAMA3):c.2415T>C (p.Ile805=) rs371968250
NM_198129.4(LAMA3):c.2670-7G>A rs778249170
NM_198129.4(LAMA3):c.2874T>G (p.Val958=) rs61751702
NM_198129.4(LAMA3):c.2937C>T (p.Ser979=) rs148470606
NM_198129.4(LAMA3):c.3027C>T (p.Ile1009=) rs372276274
NM_198129.4(LAMA3):c.3279C>T (p.Pro1093=) rs774235779
NM_198129.4(LAMA3):c.3381C>T (p.Tyr1127=) rs767385840
NM_198129.4(LAMA3):c.4160G>A (p.Arg1387Gln) rs112861599
NM_198129.4(LAMA3):c.4246G>A (p.Val1416Met) rs77331026
NM_198129.4(LAMA3):c.4758C>T (p.His1586=) rs770614208
NM_198129.4(LAMA3):c.4782T>C (p.His1594=) rs1598964989
NM_198129.4(LAMA3):c.4998+1367G>A
NM_198129.4(LAMA3):c.744C>T (p.Thr248=) rs750401726
NM_198129.4(LAMA3):c.856-5T>C rs565368053

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