ClinVar Miner

List of variants in gene MYOM1 reported by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 104
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HGVS dbSNP
NM_003803.3(MYOM1):c.*10C>T rs876657915
NM_003803.3(MYOM1):c.-9G>A rs1662315
NM_003803.3(MYOM1):c.1022G>C (p.Gly341Ala) rs8099021
NM_003803.3(MYOM1):c.1023-14G>A rs372359086
NM_003803.3(MYOM1):c.1112-11T>C rs59555146
NM_003803.3(MYOM1):c.1146C>T (p.His382=) rs2230163
NM_003803.3(MYOM1):c.1160C>T (p.Thr387Ile) rs189973743
NM_003803.3(MYOM1):c.1175_1339[3] (p.Asn446_Gly447insValGlyValThrProTyrGlyTyrAlaSerArgPheGluIleHisPheAspAspLysPheAspValSerPheGlyArgGluGlyGluThrMetSerLeuGlyCysArgValValIleThrProGluIleLysHisPheGlnProGluIleGlnTrpTyrArgAsnValGlyValThrProTyrGlyTyrAlaSerArgPheGluIleHisPheAspAspL...(Total 360))
NM_003803.3(MYOM1):c.117C>T (p.Tyr39=) rs375113650
NM_003803.3(MYOM1):c.120C>G (p.Thr40=) rs876657535
NM_003803.3(MYOM1):c.1235A>G (p.Asp412Gly) rs767444514
NM_003803.3(MYOM1):c.1338C>T (p.Asn446=) rs2230167
NM_003803.3(MYOM1):c.1340-14del rs554705715
NM_003803.3(MYOM1):c.1392G>A (p.Arg464=) rs11659820
NM_003803.3(MYOM1):c.139A>G (p.Ser47Gly) rs202145133
NM_003803.3(MYOM1):c.1455G>C (p.Arg485=) rs193006519
NM_003803.3(MYOM1):c.1466A>G (p.Tyr489Cys) rs369422118
NM_003803.3(MYOM1):c.158C>T (p.Ala53Val) rs747035411
NM_003803.3(MYOM1):c.1627G>A
NM_003803.3(MYOM1):c.1668del (p.Trp556fs) rs876657916
NM_003803.3(MYOM1):c.1799A>T (p.Glu600Val) rs9807556
NM_003803.3(MYOM1):c.1803C>T (p.Pro601=) rs371861150
NM_003803.3(MYOM1):c.1843+10T>G rs116743447
NM_003803.3(MYOM1):c.1878T>C (p.Ile626=) rs180916932
NM_003803.3(MYOM1):c.1890G>A (p.Glu630=) rs36098676
NM_003803.3(MYOM1):c.1900+3A>C rs77613865
NM_003803.3(MYOM1):c.1901-14T>C rs200115559
NM_003803.3(MYOM1):c.1917C>T (p.Gly639=) rs761762328
NM_003803.3(MYOM1):c.192G>T (p.Ala64=) rs9964300
NM_003803.3(MYOM1):c.1952G>A (p.Arg651Gln) rs184721031
NM_003803.3(MYOM1):c.1978C>G (p.Pro660Ala) rs201104206
NM_003803.3(MYOM1):c.2062A>T (p.Thr688Ser) rs188677538
NM_003803.3(MYOM1):c.2064G>A (p.Thr688=) rs374462999
NM_003803.3(MYOM1):c.2110G>A (p.Glu704Lys) rs149528866
NM_003803.3(MYOM1):c.2137C>T (p.Arg713Cys) rs375858580
NM_003803.3(MYOM1):c.2179A>G (p.Thr727Ala) rs115382168
NM_003803.3(MYOM1):c.2210-4T>G rs143030509
NM_003803.3(MYOM1):c.2350G>A (p.Glu784Lys) rs368949465
NM_003803.3(MYOM1):c.2383C>G (p.Arg795Gly) rs201618512
NM_003803.3(MYOM1):c.2384+4A>T rs73373171
NM_003803.3(MYOM1):c.2385-13G>A rs116126674
NM_003803.3(MYOM1):c.2428C>T
NM_003803.3(MYOM1):c.2506+15C>G rs1272570164
NM_003803.3(MYOM1):c.2507-22TGT[2] rs147985558
NM_003803.3(MYOM1):c.2598G>A (p.Pro866=) rs778413922
NM_003803.3(MYOM1):c.2656A>G (p.Ser886Gly) rs199900004
NM_003803.3(MYOM1):c.2673G>C (p.Leu891=) rs115240600
NM_003803.3(MYOM1):c.2697A>C (p.Val899=) rs771666952
NM_003803.3(MYOM1):c.2727G>A (p.Pro909=) rs72860212
NM_003803.3(MYOM1):c.2802A>G (p.Pro934=) rs79397275
NM_003803.3(MYOM1):c.2879T>C (p.Ile960Thr) rs1071600
NM_003803.3(MYOM1):c.290+14C>G rs7232679
NM_003803.3(MYOM1):c.290G>T (p.Gly97Val) rs568600892
NM_003803.3(MYOM1):c.297A>G (p.Thr99=) rs369402806
NM_003803.3(MYOM1):c.3038C>T (p.Ala1013Val) rs557671408
NM_003803.3(MYOM1):c.3125C>T (p.Pro1042Leu) rs761951856
NM_003803.3(MYOM1):c.3190C>T (p.His1064Tyr) rs755409090
NM_003803.3(MYOM1):c.3195C>G (p.Ser1065=) rs185366609
NM_003803.3(MYOM1):c.3278C>T (p.Ala1093Val) rs749676865
NM_003803.3(MYOM1):c.3308G>A (p.Arg1103Gln) rs186972208
NM_003803.3(MYOM1):c.335T>G (p.Leu112Trp) rs868781965
NM_003803.3(MYOM1):c.3413G>A (p.Arg1138His) rs148782330
NM_003803.3(MYOM1):c.3453T>A (p.Asp1151Glu) rs143879853
NM_003803.3(MYOM1):c.3523T>G (p.Tyr1175Asp)
NM_003803.3(MYOM1):c.3539A>G (p.Asp1180Gly) rs188319622
NM_003803.3(MYOM1):c.3548G>A (p.Arg1183Gln) rs147050513
NM_003803.3(MYOM1):c.3572A>G (p.Asn1191Ser) rs200480164
NM_003803.3(MYOM1):c.3576-5C>T rs7232329
NM_003803.3(MYOM1):c.3665A>G (p.Tyr1222Cys) rs748819463
NM_003803.3(MYOM1):c.3683-9C>T rs1060504725
NM_003803.3(MYOM1):c.3863C>T (p.Pro1288Leu) rs200808890
NM_003803.3(MYOM1):c.3945G>A (p.Thr1315=) rs75748615
NM_003803.3(MYOM1):c.4069+13C>A rs948298
NM_003803.3(MYOM1):c.4069+4A>C rs80328493
NM_003803.3(MYOM1):c.4177A>G (p.Lys1393Glu) rs371239754
NM_003803.3(MYOM1):c.4222G>A (p.Asp1408Asn) rs3765623
NM_003803.3(MYOM1):c.4351C>G (p.Leu1451Val) rs876657917
NM_003803.3(MYOM1):c.4357A>T (p.Met1453Leu) rs181642354
NM_003803.3(MYOM1):c.4358T>C (p.Met1453Thr) rs16944397
NM_003803.3(MYOM1):c.4586A>G (p.Tyr1529Cys) rs876657918
NM_003803.3(MYOM1):c.461C>T (p.Thr154Met) rs140845661
NM_003803.3(MYOM1):c.4648+7A>G rs555598943
NM_003803.3(MYOM1):c.4662C>T (p.Ala1554=) rs1143657
NM_003803.3(MYOM1):c.4672T>C (p.Phe1558Leu) rs187108957
NM_003803.3(MYOM1):c.4685+11G>T rs2298539
NM_003803.3(MYOM1):c.4718G>A (p.Arg1573Gln) rs117342470
NM_003803.3(MYOM1):c.476_479del (p.Ile159fs) rs876657920
NM_003803.3(MYOM1):c.4776C>G (p.Leu1592=) rs1143658
NM_003803.3(MYOM1):c.5001G>A (p.Glu1667=) rs376007739
NM_003803.3(MYOM1):c.5040T>C (p.Gly1680=) rs2230164
NM_003803.3(MYOM1):c.5045dup (p.Lys1683fs) rs573184538
NM_003803.3(MYOM1):c.539C>T (p.Thr180Ile) rs61735396
NM_003803.3(MYOM1):c.541T>C (p.Ser181Pro) rs1962519
NM_003803.3(MYOM1):c.590C>T (p.Thr197Met) rs142735495
NM_003803.3(MYOM1):c.644C>T (p.Thr215Met) rs2230165
NM_003803.3(MYOM1):c.64G>C (p.Val22Leu) rs1791085
NM_003803.3(MYOM1):c.660T>C (p.Ser220=) rs2230166
NM_003803.3(MYOM1):c.66G>C (p.Val22=) rs1662316
NM_003803.3(MYOM1):c.739G>A (p.Glu247Lys) rs139422575
NM_003803.3(MYOM1):c.91C>A (p.Arg31=) rs76382984
NM_003803.3(MYOM1):c.924C>A (p.Val308=) rs536739408
NM_003803.3(MYOM1):c.93G>A (p.Arg31=) rs876657536
NM_003803.3(MYOM1):c.999G>A (p.Gly333=) rs2230162
NM_003803.3(MYOM1):c.[64_66delGTGinsCTC;65T>G]

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