ClinVar Miner

List of variants in gene MYOM1 reported as uncertain significance for Hypertrophic cardiomyopathy

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Total variants: 105
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HGVS dbSNP
NC_000018.10:g.(?_3168817)_(3168981_?)dup
NM_003803.3(MYOM1):c.1022_1022+1delGGinsCA rs1555627004
NM_003803.3(MYOM1):c.1051C>T (p.Arg351Trp) rs375848036
NM_003803.3(MYOM1):c.1058C>T (p.Ser353Leu)
NM_003803.3(MYOM1):c.110C>T (p.Ala37Val) rs375155656
NM_003803.3(MYOM1):c.1139G>A (p.Arg380His)
NM_003803.3(MYOM1):c.1168C>T (p.Leu390Phe)
NM_003803.3(MYOM1):c.1204C>T (p.Arg402Trp)
NM_003803.3(MYOM1):c.1222G>A (p.Asp408Asn)
NM_003803.3(MYOM1):c.1235A>T (p.Asp412Val)
NM_003803.3(MYOM1):c.1279C>T (p.Arg427Cys) rs376648139
NM_003803.3(MYOM1):c.1288A>G (p.Ile430Val) rs764996297
NM_003803.3(MYOM1):c.1358C>T (p.Ser453Leu) rs368424215
NM_003803.3(MYOM1):c.1362A>G (p.Lys454=) rs778965112
NM_003803.3(MYOM1):c.136T>C (p.Tyr46His) rs201544310
NM_003803.3(MYOM1):c.1370A>G (p.Gln457Arg) rs757169901
NM_003803.3(MYOM1):c.1424A>C (p.Glu475Ala)
NM_003803.3(MYOM1):c.142A>T (p.Ser48Cys) rs1234403854
NM_003803.3(MYOM1):c.1438T>C (p.Tyr480His) rs763945524
NM_003803.3(MYOM1):c.1442C>G (p.Thr481Arg) rs370177143
NM_003803.3(MYOM1):c.1453C>T (p.Arg485Trp)
NM_003803.3(MYOM1):c.1466A>G (p.Tyr489Cys) rs369422118
NM_003803.3(MYOM1):c.1612G>A (p.Gly538Arg) rs374025340
NM_003803.3(MYOM1):c.1725C>A (p.Ile575=) rs780564541
NM_003803.3(MYOM1):c.1736C>T (p.Ser579Phe) rs185573271
NM_003803.3(MYOM1):c.1747C>T (p.Arg583Ter) rs765191680
NM_003803.3(MYOM1):c.175G>A (p.Glu59Lys) rs878854614
NM_003803.3(MYOM1):c.184C>T (p.Arg62Cys) rs766972653
NM_003803.3(MYOM1):c.1965G>A (p.Val655=) rs998287871
NM_003803.3(MYOM1):c.1991G>A (p.Arg664His) rs373489373
NM_003803.3(MYOM1):c.2023A>G (p.Lys675Glu) rs200179081
NM_003803.3(MYOM1):c.2086C>T (p.Arg696Cys) rs757565820
NM_003803.3(MYOM1):c.2132G>A (p.Arg711His)
NM_003803.3(MYOM1):c.2137C>T (p.Arg713Cys) rs375858580
NM_003803.3(MYOM1):c.2209+4A>G
NM_003803.3(MYOM1):c.2324C>A (p.Ala775Glu) rs765961982
NM_003803.3(MYOM1):c.2367C>G (p.Asn789Lys) rs773582739
NM_003803.3(MYOM1):c.2574G>C (p.Arg858Ser) rs1422382078
NM_003803.3(MYOM1):c.2581G>A (p.Val861Met)
NM_003803.3(MYOM1):c.2582T>G (p.Val861Gly)
NM_003803.3(MYOM1):c.2607C>G (p.Phe869Leu) rs1555620828
NM_003803.3(MYOM1):c.263C>T (p.Ser88Leu) rs758070531
NM_003803.3(MYOM1):c.2653C>G (p.Pro885Ala) rs764303814
NM_003803.3(MYOM1):c.2717A>C (p.Glu906Ala) rs760763098
NM_003803.3(MYOM1):c.2750_2751delAG (p.Gln917Argfs) rs1555620787
NM_003803.3(MYOM1):c.281C>G (p.Ser94Cys) rs761148558
NM_003803.3(MYOM1):c.2848A>G (p.Met950Val) rs184774935
NM_003803.3(MYOM1):c.2851G>T (p.Val951Phe) rs573023709
NM_003803.3(MYOM1):c.2875A>G (p.Lys959Glu) rs192365952
NM_003803.3(MYOM1):c.2920G>A (p.Glu974Lys) rs774931774
NM_003803.3(MYOM1):c.2975G>T (p.Ser992Ile)
NM_003803.3(MYOM1):c.3097G>A (p.Glu1033Lys) rs377512048
NM_003803.3(MYOM1):c.3097G>T (p.Glu1033Ter) rs377512048
NM_003803.3(MYOM1):c.3109G>A (p.Ala1037Thr) rs199817096
NM_003803.3(MYOM1):c.315A>C (p.Leu105Phe) rs991834729
NM_003803.3(MYOM1):c.3223G>A (p.Val1075Met) rs371066861
NM_003803.3(MYOM1):c.3245C>G (p.Ala1082Gly)
NM_003803.3(MYOM1):c.329C>T (p.Ser110Phe)
NM_003803.3(MYOM1):c.3325G>A (p.Val1109Ile) rs377448983
NM_003803.3(MYOM1):c.3388G>T (p.Ala1130Ser) rs375291963
NM_003803.3(MYOM1):c.3419G>A (p.Gly1140Glu) rs375843420
NM_003803.3(MYOM1):c.3475G>A (p.Glu1159Lys) rs764808541
NM_003803.3(MYOM1):c.3523T>G (p.Tyr1175Asp)
NM_003803.3(MYOM1):c.3781C>T (p.Arg1261Trp)
NM_003803.3(MYOM1):c.3782G>A (p.Arg1261Gln) rs374656485
NM_003803.3(MYOM1):c.3796G>A (p.Ala1266Thr) rs554969785
NM_003803.3(MYOM1):c.3813C>T (p.Gly1271=) rs771659817
NM_003803.3(MYOM1):c.3886C>T (p.Arg1296Ter)
NM_003803.3(MYOM1):c.3904G>A (p.Glu1302Lys) rs370699565
NM_003803.3(MYOM1):c.3914T>C (p.Met1305Thr)
NM_003803.3(MYOM1):c.395T>G (p.Leu132Trp) rs1555629260
NM_003803.3(MYOM1):c.3992T>C (p.Val1331Ala)
NM_003803.3(MYOM1):c.4007A>T (p.Asp1336Val) rs575609095
NM_003803.3(MYOM1):c.400A>G (p.Ser134Gly)
NM_003803.3(MYOM1):c.4045C>T (p.Arg1349Trp) rs762476268
NM_003803.3(MYOM1):c.409A>C (p.Met137Leu) rs765511668
NM_003803.3(MYOM1):c.4148T>C (p.Ile1383Thr) rs374491316
NM_003803.3(MYOM1):c.4177A>G (p.Lys1393Glu) rs371239754
NM_003803.3(MYOM1):c.4181A>G (p.Asp1394Gly) rs374142554
NM_003803.3(MYOM1):c.4207A>C (p.Lys1403Gln) rs779356078
NM_003803.3(MYOM1):c.4243A>G (p.Ile1415Val)
NM_003803.3(MYOM1):c.4301G>A (p.Arg1434Gln) rs776173695
NM_003803.3(MYOM1):c.431+5G>C rs772009177
NM_003803.3(MYOM1):c.4446T>G (p.Thr1482=) rs367695432
NM_003803.3(MYOM1):c.4496T>C (p.Ile1499Thr) rs1060502820
NM_003803.3(MYOM1):c.4568C>T (p.Pro1523Leu) rs761317710
NM_003803.3(MYOM1):c.4580G>T (p.Gly1527Val) rs1411286868
NM_003803.3(MYOM1):c.4685+3_4685+6delAAGT
NM_003803.3(MYOM1):c.4711C>T (p.Arg1571Cys) rs373419422
NM_003803.3(MYOM1):c.4752C>G (p.Ile1584Met)
NM_003803.3(MYOM1):c.4792G>A (p.Gly1598Arg) rs764839969
NM_003803.3(MYOM1):c.4903G>A (p.Gly1635Ser) rs200773357
NM_003803.3(MYOM1):c.500C>T (p.Ala167Val)
NM_003803.3(MYOM1):c.544A>C (p.Lys182Gln)
NM_003803.3(MYOM1):c.554C>T (p.Thr185Met) rs761722591
NM_003803.3(MYOM1):c.617A>G (p.Lys206Arg) rs548278691
NM_003803.3(MYOM1):c.617_634dup (p.Ser211_Arg212insLysGlnSerThrAlaSer) rs755975362
NM_003803.3(MYOM1):c.626C>T (p.Thr209Met)
NM_003803.3(MYOM1):c.65T>G (p.Val22Gly) rs113162857
NM_003803.3(MYOM1):c.814C>T (p.His272Tyr) rs1555628272
NM_003803.3(MYOM1):c.919C>T (p.Arg307Cys)
NM_003803.3(MYOM1):c.920G>C (p.Arg307Pro) rs199520642
NM_003803.3(MYOM1):c.928T>A (p.Trp310Arg)
NM_003803.3(MYOM1):c.977A>G (p.Tyr326Cys) rs773366188
NM_003803.3(MYOM1):c.982_984delATT (p.Ile328del) rs765548922

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