ClinVar Miner

List of variants in gene LAMA4 reported by Biesecker Lab/Human Development Section,National Institutes of Health

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Total variants: 38
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1087G>C (p.Ala363Pro) rs201431982
NM_001105206.3(LAMA4):c.1277T>C (p.Met426Thr) rs200112094
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.1633C>T (p.Arg545Cys) rs138153075
NM_001105206.3(LAMA4):c.1858G>A (p.Ala620Thr) rs374001056
NM_001105206.3(LAMA4):c.195+71_195+73del rs786205414
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2177A>T (p.Asp726Val) rs781823199
NM_001105206.3(LAMA4):c.2398C>T (p.Arg800Cys) rs202184174
NM_001105206.3(LAMA4):c.2614C>G (p.Pro872Ala) rs180931319
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917
NM_001105206.3(LAMA4):c.2912C>T (p.Ser971Phe) rs781856644
NM_001105206.3(LAMA4):c.297+2368G>A rs75992359
NM_001105206.3(LAMA4):c.3026C>A (p.Ala1009Asp) rs199618820
NM_001105206.3(LAMA4):c.3029C>T (p.Thr1010Ile) rs201431614
NM_001105206.3(LAMA4):c.3074A>G (p.Tyr1025Cys) rs370557242
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.3322C>T (p.His1108Tyr) rs201660110
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.3585T>A (p.Asp1195Glu) rs786205410
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811
NM_001105206.3(LAMA4):c.4168C>T (p.Arg1390Trp) rs200189282
NM_001105206.3(LAMA4):c.4328C>T (p.Ala1443Val) rs782696599
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.4708G>T (p.Asp1570Tyr) rs199938033
NM_001105206.3(LAMA4):c.521A>G (p.Tyr174Cys) rs202131320
NM_001105206.3(LAMA4):c.5369C>T (p.Thr1790Ile) rs786205409
NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser) rs142048329
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_001105206.3(LAMA4):c.668G>A (p.Arg223His) rs200017155
NM_001105206.3(LAMA4):c.676C>T (p.Pro226Ser) rs201820268
NM_001105206.3(LAMA4):c.832T>C (p.Trp278Arg) rs201486893
NM_001105206.3(LAMA4):c.848= (p.Asp283=) rs879974322

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