ClinVar Miner

List of variants in gene MYL3 reported as uncertain significance for Cardiomyopathy

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Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_000258.3(MYL3):c.367A>G (p.Lys123Glu) rs536445081 0.00004
NM_000258.3(MYL3):c.460C>T (p.Arg154Cys) rs143852164 0.00004
NM_000258.3(MYL3):c.466G>A (p.Val156Met) rs199474707 0.00004
NM_000258.3(MYL3):c.476C>T (p.Thr159Met) rs748832105 0.00004
NM_000258.3(MYL3):c.245C>T (p.Ala82Val) rs752549068 0.00003
NM_000258.3(MYL3):c.*6G>A rs754568155 0.00002
NM_000258.3(MYL3):c.136T>C (p.Phe46Leu) rs730880953 0.00002
NM_000258.3(MYL3):c.140C>T (p.Thr47Ile) rs778515428 0.00002
NM_000258.3(MYL3):c.152T>C (p.Ile51Thr) rs749017586 0.00002
NM_000258.3(MYL3):c.187C>T (p.Arg63Cys) rs565312070 0.00002
NM_000258.3(MYL3):c.280C>T (p.Arg94Cys) rs730880961 0.00002
NM_000258.3(MYL3):c.461G>A (p.Arg154His) rs104893749 0.00002
NM_000258.3(MYL3):c.530A>G (p.Glu177Gly) rs193922391 0.00002
NM_000258.3(MYL3):c.61C>T (p.Pro21Ser) rs779557153 0.00002
NM_000258.3(MYL3):c.106G>A (p.Glu36Lys) rs749941468 0.00001
NM_000258.3(MYL3):c.147G>T (p.Glu49Asp) rs1004231349 0.00001
NM_000258.3(MYL3):c.178C>G (p.Leu60Val) rs1367233580 0.00001
NM_000258.3(MYL3):c.188G>A (p.Arg63His) rs139354105 0.00001
NM_000258.3(MYL3):c.193C>T (p.Pro65Ser) rs730880960 0.00001
NM_000258.3(MYL3):c.220G>A (p.Gly74Arg) rs730880956 0.00001
NM_000258.3(MYL3):c.235G>A (p.Val79Ile) rs150634297 0.00001
NM_000258.3(MYL3):c.241C>T (p.Arg81Trp) rs761891361 0.00001
NM_000258.3(MYL3):c.26A>G (p.Lys9Arg) rs1025864971 0.00001
NM_000258.3(MYL3):c.307G>A (p.Glu103Lys) rs1479071663 0.00001
NM_000258.3(MYL3):c.502G>A (p.Glu168Lys) rs1376871183 0.00001
NM_000258.3(MYL3):c.517A>G (p.Met173Val) rs199474708 0.00001
NM_000258.3(MYL3):c.521C>T (p.Ala174Val) rs763216044 0.00001
NM_000258.3(MYL3):c.557A>C (p.Glu186Ala) rs374329098 0.00001
NM_000258.3(MYL3):c.560-15T>G rs1041055773 0.00001
NM_000258.3(MYL3):c.-15T>A
NM_000258.3(MYL3):c.124A>T (p.Ile42Phe) rs1322033572
NM_000258.3(MYL3):c.127A>G (p.Lys43Glu) rs2106914291
NM_000258.3(MYL3):c.129+1G>T rs112545893
NM_000258.3(MYL3):c.158-3C>G rs111668273
NM_000258.3(MYL3):c.170C>A (p.Ala57Asp) rs139794067
NM_000258.3(MYL3):c.170C>G (p.Ala57Gly) rs139794067
NM_000258.3(MYL3):c.184G>A (p.Asp62Asn) rs730880954
NM_000258.3(MYL3):c.1A>G (p.Met1Val)
NM_000258.3(MYL3):c.206T>A (p.Met69Lys) rs1575498236
NM_000258.3(MYL3):c.214A>G (p.Thr72Ala)
NM_000258.3(MYL3):c.229G>A (p.Gly77Arg) rs1559520411
NM_000258.3(MYL3):c.274G>A (p.Val92Met) rs770961856
NM_000258.3(MYL3):c.307+3A>G rs2106909563
NM_000258.3(MYL3):c.307+4G>T
NM_000258.3(MYL3):c.310C>A (p.Leu104Ile)
NM_000258.3(MYL3):c.31G>A (p.Asp11Asn)
NM_000258.3(MYL3):c.320A>G (p.Lys107Arg) rs1701969420
NM_000258.3(MYL3):c.338C>T (p.Thr113Ile) rs397516278
NM_000258.3(MYL3):c.344T>C (p.Leu115Pro)
NM_000258.3(MYL3):c.370A>T (p.Asn124Tyr) rs1278498849
NM_000258.3(MYL3):c.397T>A (p.Phe133Ile) rs1553639870
NM_000258.3(MYL3):c.40A>C (p.Lys14Gln) rs1702011948
NM_000258.3(MYL3):c.413G>A (p.Arg138Gln) rs1057524652
NM_000258.3(MYL3):c.419T>G (p.Phe140Cys) rs1559520147
NM_000258.3(MYL3):c.421G>T (p.Asp141Tyr) rs1483805765
NM_000258.3(MYL3):c.430G>A (p.Gly144Ser)
NM_000258.3(MYL3):c.457del (p.Leu153fs) rs1064793448
NM_000258.3(MYL3):c.482-9T>A rs1559519895
NM_000258.3(MYL3):c.484G>A (p.Glu162Lys) rs371642547
NM_000258.3(MYL3):c.488G>A (p.Arg163Lys) rs752165383
NM_000258.3(MYL3):c.499G>A (p.Asp167Asn) rs1701956074
NM_000258.3(MYL3):c.49C>T (p.Pro17Ser) rs1702011848
NM_000258.3(MYL3):c.4G>T (p.Ala2Ser) rs148310342
NM_000258.3(MYL3):c.520G>C (p.Ala174Pro) rs397516279
NM_000258.3(MYL3):c.52A>G (p.Lys18Glu) rs1702011793
NM_000258.3(MYL3):c.539A>G (p.Asn180Ser) rs1575497410
NM_000258.3(MYL3):c.551A>G (p.Asn184Ser)
NM_000258.3(MYL3):c.55G>T (p.Ala19Ser)
NM_000258.3(MYL3):c.560-1G>A rs1701953138
NM_000258.3(MYL3):c.577A>G (p.Met193Val) rs1701951996
NM_000258.3(MYL3):c.65C>T (p.Ala22Val) rs2106914529
NM_000258.3(MYL3):c.77C>G (p.Pro26Arg) rs1702011145
NM_000258.3(MYL3):c.79C>G (p.Pro27Ala) rs1248338056
NM_000258.3(MYL3):c.80C>G (p.Pro27Arg) rs1210373907
NM_000258.3(MYL3):c.8C>A (p.Pro3His) rs536404643

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