ClinVar Miner

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

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Total variants: 23
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HGVS dbSNP
NM_003803.3(MYOM1):c.*10C>T rs876657915
NM_003803.3(MYOM1):c.1175_1339[3] (p.Asn446_Gly447insValGlyValThrProTyrGlyTyrAlaSerArgPheGluIleHisPheAspAspLysPheAspValSerPheGlyArgGluGlyGluThrMetSerLeuGlyCysArgValValIleThrProGluIleLysHisPheGlnProGluIleGlnTrpTyrArgAsnValGlyValThrProTyrGlyTyrAlaSerArgPheGluIleHisPheAspAspL...(Total 360))
NM_003803.3(MYOM1):c.1235A>G (p.Asp412Gly) rs767444514
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.1668del (p.Trp556fs) rs876657916
NM_003803.3(MYOM1):c.2137C>T (p.Arg713Cys) rs375858580
NM_003803.3(MYOM1):c.2383C>G (p.Arg795Gly) rs201618512
NM_003803.3(MYOM1):c.2428C>T
NM_003803.3(MYOM1):c.3125C>T (p.Pro1042Leu) rs761951856
NM_003803.3(MYOM1):c.3278C>T (p.Ala1093Val) rs749676865
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.3523T>G (p.Tyr1175Asp)
NM_003803.3(MYOM1):c.3548G>A (p.Arg1183Gln) rs147050513
NM_003803.3(MYOM1):c.3665A>G (p.Tyr1222Cys) rs748819463
NM_003803.3(MYOM1):c.3863C>T (p.Pro1288Leu) rs200808890
NM_003803.3(MYOM1):c.4177A>G (p.Lys1393Glu) rs371239754
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.4586A>G (p.Tyr1529Cys) rs876657918
NM_003803.3(MYOM1):c.476_479del (p.Ile159fs) rs876657920
NM_003803.3(MYOM1):c.[64_66delGTGinsCTC;65T>G]

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