ClinVar Miner

List of variants in gene LAMA4 reported by Fulgent Genetics, Fulgent Genetics

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Gene type:
ClinVar version:
Total variants: 125
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.531C>T (p.Pro177=) rs61742228 0.01462
NM_001105206.3(LAMA4):c.4287+15C>T rs116361180 0.01137
NM_001105206.3(LAMA4):c.422+20G>T rs188820838 0.00271
NM_001105206.3(LAMA4):c.4314A>C (p.Ser1438=) rs77367833 0.00251
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180 0.00210
NM_001105206.3(LAMA4):c.2493+15G>T rs77901141 0.00178
NM_001105206.3(LAMA4):c.196-9C>T rs144850734 0.00174
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048 0.00151
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488 0.00091
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862 0.00052
NM_001105206.3(LAMA4):c.5340A>G (p.Thr1780=) rs139241892 0.00050
NM_001105206.3(LAMA4):c.503G>A (p.Arg168Lys) rs200368819 0.00023
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442 0.00022
NM_001105206.3(LAMA4):c.578C>T (p.Ser193Leu) rs147870828 0.00022
NM_001105206.3(LAMA4):c.1298G>A (p.Arg433His) rs369658574 0.00015
NM_001105206.3(LAMA4):c.4792G>T (p.Ala1598Ser) rs202176359 0.00015
NM_001105206.3(LAMA4):c.1541G>A (p.Arg514Gln) rs146358872 0.00014
NM_001105206.3(LAMA4):c.4493G>A (p.Arg1498His) rs147556641 0.00014
NM_001105206.3(LAMA4):c.910G>A (p.Gly304Arg) rs191391557 0.00014
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val) rs137893207 0.00013
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320 0.00012
NM_001105206.3(LAMA4):c.5270C>T (p.Pro1757Leu) rs200177134 0.00012
NM_001105206.3(LAMA4):c.1788C>A (p.Asp596Glu) rs145986920 0.00011
NM_001105206.3(LAMA4):c.3283-3C>G rs374159760 0.00011
NM_001105206.3(LAMA4):c.5345G>A (p.Arg1782His) rs782638314 0.00011
NM_001105206.3(LAMA4):c.952A>G (p.Ile318Val) rs141372605 0.00011
NM_001105206.3(LAMA4):c.1390C>G (p.His464Asp) rs151119304 0.00010
NM_001105206.3(LAMA4):c.1522G>A (p.Ala508Thr) rs139730568 0.00008
NM_001105206.3(LAMA4):c.221C>A (p.Thr74Asn) rs782226255 0.00008
NM_001105206.3(LAMA4):c.2599C>A (p.Pro867Thr) rs782162498 0.00008
NM_001105206.3(LAMA4):c.4199A>G (p.Tyr1400Cys) rs782041997 0.00008
NM_001105206.3(LAMA4):c.4715T>G (p.Leu1572Arg) rs782367093 0.00008
NM_001105206.3(LAMA4):c.1858G>A (p.Ala620Thr) rs374001056 0.00007
NM_001105206.3(LAMA4):c.196-11G>A rs374364713 0.00007
NM_001105206.3(LAMA4):c.1166A>G (p.His389Arg) rs782618362 0.00006
NM_001105206.3(LAMA4):c.1420G>A (p.Val474Ile) rs375981026 0.00006
NM_001105206.3(LAMA4):c.1551+8G>A rs782128294 0.00006
NM_001105206.3(LAMA4):c.1634G>A (p.Arg545His) rs143937452 0.00006
NM_001105206.3(LAMA4):c.167C>T (p.Ala56Val) rs372763422 0.00006
NM_001105206.3(LAMA4):c.4583G>T (p.Arg1528Leu) rs782805733 0.00006
NM_001105206.3(LAMA4):c.4679G>A (p.Arg1560Gln) rs397516732 0.00006
NM_001105206.3(LAMA4):c.5393T>C (p.Ile1798Thr) rs377204776 0.00006
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329 0.00006
NM_001105206.3(LAMA4):c.672C>T (p.Cys224=) rs781903380 0.00006
NM_001105206.3(LAMA4):c.928C>G (p.His310Asp) rs374968791 0.00006
NM_001105206.3(LAMA4):c.1837A>G (p.Met613Val) rs371083384 0.00005
NM_001105206.3(LAMA4):c.2626G>A (p.Glu876Lys) rs147206383 0.00005
NM_001105206.3(LAMA4):c.3406T>C (p.Tyr1136His) rs148462898 0.00005
NM_001105206.3(LAMA4):c.4208C>T (p.Pro1403Leu) rs1255830395 0.00005
NM_001105206.3(LAMA4):c.4572G>C (p.Leu1524Phe) rs145315273 0.00005
NM_001105206.3(LAMA4):c.1503T>A (p.Asp501Glu) rs370194991 0.00004
NM_001105206.3(LAMA4):c.1769C>G (p.Ala590Gly) rs782394010 0.00004
NM_001105206.3(LAMA4):c.1843G>A (p.Gly615Arg) rs377499201 0.00004
NM_001105206.3(LAMA4):c.2143G>T (p.Ala715Ser) rs140710429 0.00004
NM_001105206.3(LAMA4):c.2402C>T (p.Thr801Met) rs782325644 0.00004
NM_001105206.3(LAMA4):c.4346G>A (p.Arg1449Gln) rs782695193 0.00004
NM_001105206.3(LAMA4):c.5005A>G (p.Lys1669Glu) rs782716382 0.00004
NM_001105206.3(LAMA4):c.838C>A (p.Leu280Met) rs369332778 0.00004
NM_001105206.3(LAMA4):c.967-16A>G rs80110492 0.00004
NM_001105206.3(LAMA4):c.1057G>A (p.Val353Ile) rs781919461 0.00003
NM_001105206.3(LAMA4):c.2302C>T (p.His768Tyr) rs140107576 0.00003
NM_001105206.3(LAMA4):c.2635G>C (p.Asp879His) rs371253565 0.00003
NM_001105206.3(LAMA4):c.3697-3C>T rs536295629 0.00003
NM_001105206.3(LAMA4):c.4235T>C (p.Leu1412Pro) rs376369192 0.00003
NM_001105206.3(LAMA4):c.5254A>G (p.Asn1752Asp) rs371370857 0.00003
NM_001105206.3(LAMA4):c.964A>C (p.Lys322Gln) rs1375382054 0.00003
NM_001105206.3(LAMA4):c.1808A>T (p.Glu603Val) rs781829812 0.00002
NM_001105206.3(LAMA4):c.1813A>G (p.Ser605Gly) rs112884471 0.00002
NM_001105206.3(LAMA4):c.191C>T (p.Ala64Val) rs376091454 0.00002
NM_001105206.3(LAMA4):c.2054C>T (p.Ser685Phe) rs369776441 0.00002
NM_001105206.3(LAMA4):c.2225A>G (p.Asn742Ser) rs374279330 0.00002
NM_001105206.3(LAMA4):c.3238C>T (p.Arg1080Ter) rs372615994 0.00002
NM_001105206.3(LAMA4):c.3277A>G (p.Asn1093Asp) rs782550866 0.00002
NM_001105206.3(LAMA4):c.4183G>A (p.Val1395Ile) rs782627670 0.00002
NM_001105206.3(LAMA4):c.475G>A (p.Glu159Lys) rs540626879 0.00002
NM_001105206.3(LAMA4):c.4972G>A (p.Val1658Met) rs149555058 0.00002
NM_001105206.3(LAMA4):c.5029C>T (p.Arg1677Cys) rs587753056 0.00002
NM_001105206.3(LAMA4):c.133del (p.Gln45fs) rs1341828711 0.00001
NM_001105206.3(LAMA4):c.1364G>T (p.Ser455Ile) rs782547342 0.00001
NM_001105206.3(LAMA4):c.1436A>T (p.Asp479Val) rs781939403 0.00001
NM_001105206.3(LAMA4):c.1455G>T (p.Leu485Phe) rs782305599 0.00001
NM_001105206.3(LAMA4):c.1525A>C (p.Thr509Pro) rs951225457 0.00001
NM_001105206.3(LAMA4):c.153C>A (p.Ser51Arg) rs782192817 0.00001
NM_001105206.3(LAMA4):c.1582G>A (p.Glu528Lys) rs782385471 0.00001
NM_001105206.3(LAMA4):c.1778A>G (p.His593Arg) rs751004946 0.00001
NM_001105206.3(LAMA4):c.1867G>A (p.Ala623Thr) rs782574915 0.00001
NM_001105206.3(LAMA4):c.203A>G (p.Asn68Ser) rs782428669 0.00001
NM_001105206.3(LAMA4):c.2305T>C (p.Phe769Leu) rs1554334959 0.00001
NM_001105206.3(LAMA4):c.2527G>C (p.Ala843Pro) rs536755553 0.00001
NM_001105206.3(LAMA4):c.267C>T (p.Asn89=) rs727503114 0.00001
NM_001105206.3(LAMA4):c.3109C>T (p.Arg1037Ter) rs782727584 0.00001
NM_001105206.3(LAMA4):c.3311A>G (p.Asn1104Ser) rs542157463 0.00001
NM_001105206.3(LAMA4):c.4008G>C (p.Lys1336Asn) rs373047072 0.00001
NM_001105206.3(LAMA4):c.4052A>G (p.Lys1351Arg) rs876657843 0.00001
NM_001105206.3(LAMA4):c.4059T>A (p.Phe1353Leu) rs782273793 0.00001
NM_001105206.3(LAMA4):c.4328C>T (p.Ala1443Val) rs782696599 0.00001
NM_001105206.3(LAMA4):c.4505G>A (p.Arg1502His) rs781976795 0.00001
NM_001105206.3(LAMA4):c.4607G>T (p.Gly1536Val) rs368316926 0.00001
NM_001105206.3(LAMA4):c.4977T>C (p.Val1659=) rs199593652 0.00001
NM_001105206.3(LAMA4):c.5062G>A (p.Gly1688Ser) rs782194407 0.00001
NM_001105206.3(LAMA4):c.5206+1G>A rs368035482 0.00001
NM_001105206.3(LAMA4):c.676C>T (p.Pro226Ser) rs201820268 0.00001
NM_001105206.3(LAMA4):c.757G>A (p.Gly253Arg) rs377633183 0.00001
NM_001105206.3(LAMA4):c.913G>A (p.Ala305Thr) rs782325733 0.00001
NM_001105206.3(LAMA4):c.944A>G (p.Asn315Ser) rs1029188462 0.00001
NM_001105206.3(LAMA4):c.1163C>A (p.Ala388Asp) rs1355664776
NM_001105206.3(LAMA4):c.1419C>T (p.Val473=) rs782796474
NM_001105206.3(LAMA4):c.2417G>A (p.Arg806Gln) rs1554334150
NM_001105206.3(LAMA4):c.247G>C (p.Asp83His) rs531319918
NM_001105206.3(LAMA4):c.2493G>A (p.Lys831=) rs869025450
NM_001105206.3(LAMA4):c.307C>T (p.Arg103Trp) rs138176093
NM_001105206.3(LAMA4):c.308G>A (p.Arg103Gln) rs782029414
NM_001105206.3(LAMA4):c.3704G>A (p.Arg1235His) rs559725422
NM_001105206.3(LAMA4):c.373G>T (p.Ala125Ser) rs529185662
NM_001105206.3(LAMA4):c.449dup (p.Asn150fs) rs1249093492
NM_001105206.3(LAMA4):c.4683_4684del (p.Arg1562fs) rs1554325284
NM_001105206.3(LAMA4):c.4696C>T (p.Arg1566Ter) rs1554325261
NM_001105206.3(LAMA4):c.4967G>T (p.Gly1656Val) rs41289900
NM_001105206.3(LAMA4):c.5269C>T (p.Pro1757Ser) rs782001026
NM_001105206.3(LAMA4):c.673G>A (p.Ala225Thr) rs782121531
NM_001105206.3(LAMA4):c.730G>A (p.Gly244Arg) rs147078770
NM_001105206.3(LAMA4):c.730G>C (p.Gly244Arg) rs147078770
NM_001105206.3(LAMA4):c.85G>C (p.Asp29His) rs150662822
NM_001105206.3(LAMA4):c.868T>C (p.Ser290Pro) rs782433369
NM_001105206.3(LAMA4):c.868T>G (p.Ser290Ala) rs782433369

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