ClinVar Miner

List of variants in gene LAMA4 reported as benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 38
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HGVS dbSNP
NM_001105206.3(LAMA4):c.1035G>A (p.Thr345=) rs147069572
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515
NM_001105206.3(LAMA4):c.1326C>T (p.Leu442=) rs3752580
NM_001105206.3(LAMA4):c.1357+4G>T rs6917763
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.1647A>C (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1710T>C (p.Ser570=) rs3752577
NM_001105206.3(LAMA4):c.195+144T>C rs147118520
NM_001105206.3(LAMA4):c.196-12T>C rs78871662
NM_001105206.3(LAMA4):c.2493+15G>T rs77901141
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917
NM_001105206.3(LAMA4):c.297+8G>A rs200595773
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
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.4065C>T (p.Phe1355=) rs34753919
NM_001105206.3(LAMA4):c.4173T>C (p.Tyr1391=) rs35042032
NM_001105206.3(LAMA4):c.423-10C>T rs75058449
NM_001105206.3(LAMA4):c.423-4T>G rs79008328
NM_001105206.3(LAMA4):c.4287+15C>T rs116361180
NM_001105206.3(LAMA4):c.4314A>C (p.Ser1438=) rs77367833
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+8G>T rs184220860
NM_001105206.3(LAMA4):c.4716C>T (p.Leu1572=) rs35679345
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=) rs148517180
NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=) rs1050353
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.5443G>A (p.Val1815Ile) rs3734292
NM_001105206.3(LAMA4):c.651C>T (p.Thr217=) rs2072021
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

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