ClinVar Miner

List of variants in gene MYOM1 reported as likely benign for Hypertrophic cardiomyopathy

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Gene type:
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Total variants: 65
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HGVS dbSNP
NM_003803.3(MYOM1):c.1062G>A (p.Ala354=) rs763462534
NM_003803.3(MYOM1):c.1086G>C (p.Ser362=) rs371620091
NM_003803.3(MYOM1):c.1112-4C>T rs138604278
NM_003803.3(MYOM1):c.1125G>A (p.Glu375=) rs1060504723
NM_003803.3(MYOM1):c.1175-4C>A rs1437226766
NM_003803.3(MYOM1):c.1340-4C>A rs534659625
NM_003803.3(MYOM1):c.1397C>T (p.Thr466Met) rs561012778
NM_003803.3(MYOM1):c.1606G>A (p.Asp536Asn) rs367903122
NM_003803.3(MYOM1):c.1733G>T (p.Arg578Leu) rs200374196
NM_003803.3(MYOM1):c.1797C>T (p.Ser599=) rs370022510
NM_003803.3(MYOM1):c.1813C>G (p.Leu605Val) rs200153557
NM_003803.3(MYOM1):c.1900+6_1900+8del rs754148244
NM_003803.3(MYOM1):c.1901-4T>G rs1054418598
NM_003803.3(MYOM1):c.1911G>A (p.Val637=) rs1166836325
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.2025+10T>G rs972434580
NM_003803.3(MYOM1):c.2064G>A (p.Thr688=) rs374462999
NM_003803.3(MYOM1):c.2079G>A (p.Lys693=) rs1014448013
NM_003803.3(MYOM1):c.2087G>A (p.Arg696His) rs767192545
NM_003803.3(MYOM1):c.2221G>C (p.Ala741Pro) rs546357155
NM_003803.3(MYOM1):c.2295C>T (p.Ala765=) rs927104464
NM_003803.3(MYOM1):c.2385-9T>C rs199829674
NM_003803.3(MYOM1):c.2656A>G (p.Ser886Gly) rs199900004
NM_003803.3(MYOM1):c.2877G>A (p.Lys959=) rs755157204
NM_003803.3(MYOM1):c.2895T>C (p.Ile965=) rs1453527364
NM_003803.3(MYOM1):c.3003G>A (p.Leu1001=) rs754487227
NM_003803.3(MYOM1):c.3010A>G (p.Asn1004Asp) rs543434883
NM_003803.3(MYOM1):c.3063G>A (p.Ala1021=) rs373744359
NM_003803.3(MYOM1):c.3084C>T (p.Cys1028=) rs750152279
NM_003803.3(MYOM1):c.3129C>T (p.His1043=) rs372294428
NM_003803.3(MYOM1):c.3183G>A (p.Pro1061=) rs374873325
NM_003803.3(MYOM1):c.3189C>G (p.Val1063=) rs1060504727
NM_003803.3(MYOM1):c.3231G>A (p.Leu1077=) rs1060504724
NM_003803.3(MYOM1):c.3243G>A (p.Lys1081=) rs1060504726
NM_003803.3(MYOM1):c.3291C>T (p.Asn1097=) rs201092091
NM_003803.3(MYOM1):c.3300G>A (p.Leu1100=) rs373624207
NM_003803.3(MYOM1):c.3543T>C (p.Ser1181=) rs1252354401
NM_003803.3(MYOM1):c.3548G>A (p.Arg1183Gln) rs147050513
NM_003803.3(MYOM1):c.3579G>A (p.Thr1193=) rs575759850
NM_003803.3(MYOM1):c.3618T>C (p.Gly1206=) rs1555617218
NM_003803.3(MYOM1):c.3683-9C>T rs1060504725
NM_003803.3(MYOM1):c.387A>G (p.Lys129=) rs370293379
NM_003803.3(MYOM1):c.4251+7G>A rs377515296
NM_003803.3(MYOM1):c.4379-4T>G rs755014620
NM_003803.3(MYOM1):c.4672T>C (p.Phe1558Leu) rs187108957
NM_003803.3(MYOM1):c.4740C>T (p.Asp1580=) rs201979586
NM_003803.3(MYOM1):c.4800G>A (p.Pro1600=) rs368423483
NM_003803.3(MYOM1):c.4806G>A (p.Pro1602=) rs376121702
NM_003803.3(MYOM1):c.4815G>A (p.Ser1605=) rs763565843
NM_003803.3(MYOM1):c.4827C>T (p.Asn1609=) rs745895344
NM_003803.3(MYOM1):c.4830G>A (p.Glu1610=) rs1555613121
NM_003803.3(MYOM1):c.4908G>A (p.Val1636=) rs531803971
NM_003803.3(MYOM1):c.4914C>T (p.Thr1638=) rs368172542
NM_003803.3(MYOM1):c.4962G>A (p.Ser1654=) rs774192177
NM_003803.3(MYOM1):c.5001G>A (p.Glu1667=) rs376007739
NM_003803.3(MYOM1):c.5045dup (p.Lys1683fs) rs573184538
NM_003803.3(MYOM1):c.568_603del (p.Thr190_Gln201del) rs745347160
NM_003803.3(MYOM1):c.572C>T (p.Thr191Met) rs191505313
NM_003803.3(MYOM1):c.609A>G (p.Thr203=) rs562448650
NM_003803.3(MYOM1):c.645G>A (p.Thr215=) rs764706590
NM_003803.3(MYOM1):c.648A>G (p.Ala216=) rs1060504728
NM_003803.3(MYOM1):c.822C>T (p.Leu274=) rs201409582
NM_003803.3(MYOM1):c.93G>A (p.Arg31=) rs876657536
NM_003803.3(MYOM1):c.992G>A (p.Arg331Gln) rs199610460

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