ClinVar Miner

List of variants in gene MYH7 reported by Ambry Genetics

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Gene type:
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Total variants: 203
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HGVS dbSNP
NM_000257.4(MYH7):c.1002C>T (p.Asn334=) rs34803781
NM_000257.4(MYH7):c.1046T>C (p.Met349Thr) rs121913640
NM_000257.4(MYH7):c.1051A>G (p.Lys351Glu) rs730880864
NM_000257.4(MYH7):c.1060G>A (p.Gly354Ser) rs727503270
NM_000257.4(MYH7):c.1062C>T (p.Gly354=) rs735712
NM_000257.4(MYH7):c.1063G>A (p.Ala355Thr) rs397516088
NM_000257.4(MYH7):c.1095G>A (p.Lys365=) rs735711
NM_000257.4(MYH7):c.1106G>A (p.Arg369Gln) rs397516089
NM_000257.4(MYH7):c.1119G>A (p.Ala373=) rs572672362
NM_000257.4(MYH7):c.1128C>T (p.Asp376=) rs2231126
NM_000257.4(MYH7):c.1166G>A (p.Gly389Glu) rs727503268
NM_000257.4(MYH7):c.1184T>G (p.Leu395Arg) rs1555338374
NM_000257.4(MYH7):c.1191G>A (p.Lys397=) rs139506719
NM_000257.4(MYH7):c.1207C>T (p.Arg403Trp) rs3218714
NM_000257.4(MYH7):c.1230C>T (p.Tyr410=) rs150885220
NM_000257.4(MYH7):c.1231G>A (p.Val411Ile) rs730880868
NM_000257.4(MYH7):c.1258-3_1258-2delinsAT rs1555338344
NM_000257.4(MYH7):c.1301G>A (p.Arg434Lys) rs786205356
NM_000257.4(MYH7):c.1323G>A (p.Thr441=) rs397516096
NM_000257.4(MYH7):c.1324C>T (p.Arg442Cys) rs148808089
NM_000257.4(MYH7):c.1334C>T (p.Ala445Val) rs752349938
NM_000257.4(MYH7):c.1357C>T (p.Arg453Cys) rs121913625
NM_000257.4(MYH7):c.135G>C (p.Glu45Asp) rs397516102
NM_000257.4(MYH7):c.1370T>C (p.Ile457Thr) rs397516103
NM_000257.4(MYH7):c.1395C>G (p.Phe465Leu) rs45508293
NM_000257.4(MYH7):c.1395C>T (p.Phe465=) rs45508293
NM_000257.4(MYH7):c.1435A>G (p.Asn479Asp) rs1555338261
NM_000257.4(MYH7):c.1477A>G (p.Met493Val) rs730880875
NM_000257.4(MYH7):c.1491G>T (p.Glu497Asp) rs267606911
NM_000257.4(MYH7):c.153C>T (p.Ile51=) rs373145667
NM_000257.4(MYH7):c.1588A>G (p.Ile530Val) rs771831848
NM_000257.4(MYH7):c.1598T>A (p.Ile533Asn) rs397516114
NM_000257.4(MYH7):c.1605A>G (p.Glu535=) rs2069543
NM_000257.4(MYH7):c.161G>C (p.Arg54Pro) rs397516117
NM_000257.4(MYH7):c.1632C>T (p.Thr544=) rs587781089
NM_000257.4(MYH7):c.1633G>A (p.Asp545Asn) rs564101364
NM_000257.4(MYH7):c.1671G>A (p.Leu557=) rs149386750
NM_000257.4(MYH7):c.1681G>A (p.Ala561Thr) rs730880878
NM_000257.4(MYH7):c.1699C>T (p.Arg567Cys) rs771771163
NM_000257.4(MYH7):c.1750G>A (p.Gly584Ser) rs121913626
NM_000257.4(MYH7):c.1753A>T (p.Ile585Phe) rs886038845
NM_000257.4(MYH7):c.1755C>A (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.1767C>T (p.Asn589=) rs3729816
NM_000257.4(MYH7):c.1795del (p.Asp599fs) rs730880936
NM_000257.4(MYH7):c.1805A>G (p.Asn602Ser) rs730880880
NM_000257.4(MYH7):c.1816G>A (p.Val606Met) rs121913627
NM_000257.4(MYH7):c.1876G>A (p.Gly626Arg) rs876661370
NM_000257.4(MYH7):c.189C>T (p.Thr63=) rs2069540
NM_000257.4(MYH7):c.1982A>G (p.Asn661Ser) rs1060501435
NM_000257.4(MYH7):c.1987C>T (p.Arg663Cys) rs397516127
NM_000257.4(MYH7):c.1988G>A (p.Arg663His) rs371898076
NM_000257.4(MYH7):c.2011C>T (p.Arg671Cys) rs727503263
NM_000257.4(MYH7):c.2080C>T (p.Arg694Cys) rs727504240
NM_000257.4(MYH7):c.2081G>A (p.Arg694His) rs886039030
NM_000257.4(MYH7):c.2091T>C (p.Gly697=) rs140380523
NM_000257.4(MYH7):c.2155C>T (p.Arg719Trp) rs121913637
NM_000257.4(MYH7):c.2156G>A (p.Arg719Gln) rs121913641
NM_000257.4(MYH7):c.2162+4G>A rs145738465
NM_000257.4(MYH7):c.2167C>T (p.Arg723Cys) rs121913630
NM_000257.4(MYH7):c.2207T>C (p.Ile736Thr) rs727503261
NM_000257.4(MYH7):c.2221G>A (p.Gly741Arg) rs121913632
NM_000257.4(MYH7):c.2221G>C (p.Gly741Arg) rs121913632
NM_000257.4(MYH7):c.2221G>T (p.Gly741Trp) rs121913632
NM_000257.4(MYH7):c.22G>A (p.Val8Ile) rs754388460
NM_000257.4(MYH7):c.2302G>A (p.Gly768Arg) rs727503260
NM_000257.4(MYH7):c.2332G>A (p.Asp778Asn) rs730880895
NM_000257.4(MYH7):c.2334C>A (p.Asp778Glu) rs2069544
NM_000257.4(MYH7):c.2334C>T (p.Asp778=) rs2069544
NM_000257.4(MYH7):c.2345G>A (p.Ser782Asn) rs886039185
NM_000257.4(MYH7):c.2348G>A (p.Arg783His) rs397516142
NM_000257.4(MYH7):c.2349C>T (p.Arg783=) rs139882431
NM_000257.4(MYH7):c.2358G>T (p.Thr786=) rs36211714
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.2389G>A (p.Ala797Thr) rs3218716
NM_000257.4(MYH7):c.240C>A (p.Asn80Lys) rs200493975
NM_000257.4(MYH7):c.2423+1G>A rs113580172
NM_000257.4(MYH7):c.2446T>C (p.Trp816Arg) rs1555337763
NM_000257.4(MYH7):c.2480G>T (p.Trp827Leu) rs542565151
NM_000257.4(MYH7):c.2508C>G (p.Ile836Met) rs772442923
NM_000257.4(MYH7):c.2526T>C (p.Ser842=) rs554560162
NM_000257.4(MYH7):c.2536G>C (p.Glu846Gln) rs730880748
NM_000257.4(MYH7):c.2539A>G (p.Lys847Glu) rs727504310
NM_000257.4(MYH7):c.2539_2541del (p.Lys847del) rs397516155
NM_000257.4(MYH7):c.2548G>A (p.Ala850Thr) rs1060499880
NM_000257.4(MYH7):c.2566T>C (p.Phe856Leu) rs1555337717
NM_000257.4(MYH7):c.2573G>C (p.Arg858Pro) rs2856897
NM_000257.4(MYH7):c.2602G>C (p.Ala868Pro) rs727504356
NM_000257.4(MYH7):c.2618T>C (p.Leu873Pro) rs1555337701
NM_000257.4(MYH7):c.261C>T (p.Ile87=) rs148560996
NM_000257.4(MYH7):c.2649_2651GAA[1] (p.Lys884del) rs193922387
NM_000257.4(MYH7):c.2666T>A (p.Leu889His) rs886038813
NM_000257.4(MYH7):c.2681A>G (p.Glu894Gly) rs397516161
NM_000257.4(MYH7):c.2711G>A (p.Arg904His) rs397516165
NM_000257.4(MYH7):c.2717A>G (p.Asp906Gly) rs267606908
NM_000257.4(MYH7):c.2722C>G (p.Leu908Val) rs121913631
NM_000257.4(MYH7):c.2734A>G (p.Lys912Glu) rs730880758
NM_000257.4(MYH7):c.2736G>T (p.Lys912Asn) rs1555337597
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716
NM_000257.4(MYH7):c.2770G>A (p.Glu924Lys) rs121913628
NM_000257.4(MYH7):c.2782G>A (p.Asp928Asn) rs727503252
NM_000257.4(MYH7):c.2788G>A (p.Glu930Lys) rs397516171
NM_000257.4(MYH7):c.2863G>A (p.Asp955Asn) rs886039204
NM_000257.4(MYH7):c.2868T>A (p.Asp956Glu) rs140718120
NM_000257.4(MYH7):c.2877G>A (p.Leu959=) rs886039162
NM_000257.4(MYH7):c.2882T>G (p.Leu961Arg) rs727504374
NM_000257.4(MYH7):c.2886del (p.Val964fs) rs886038901
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu) rs45496496
NM_000257.4(MYH7):c.2891T>C (p.Val964Ala) rs778517353
NM_000257.4(MYH7):c.2907C>T (p.His969=) rs142573531
NM_000257.4(MYH7):c.2931C>T (p.Asn977=) rs757313728
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.2967T>C (p.Ile989=) rs7157716
NM_000257.4(MYH7):c.3020T>C (p.Leu1007Pro) rs730880763
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=) rs145379951
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=) rs45540831
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643
NM_000257.4(MYH7):c.3158G>A (p.Arg1053Gln) rs587782962
NM_000257.4(MYH7):c.3169G>A (p.Gly1057Ser) rs397516179
NM_000257.4(MYH7):c.3172G>A (p.Asp1058Asn) rs730880770
NM_000257.4(MYH7):c.3240G>A (p.Leu1080=) rs776886972
NM_000257.4(MYH7):c.3261G>A (p.Leu1087=) rs371937608
NM_000257.4(MYH7):c.3273C>T (p.Asn1091=) rs200664031
NM_000257.4(MYH7):c.327C>T (p.Tyr109=) rs36211408
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr) rs45478699
NM_000257.4(MYH7):c.3301G>A (p.Gly1101Ser) rs367546859
NM_000257.4(MYH7):c.3320A>C (p.Lys1107Thr) rs886038988
NM_000257.4(MYH7):c.3336+3G>A rs397516180
NM_000257.4(MYH7):c.3337-4dup rs45504498
NM_000257.4(MYH7):c.3351G>A (p.Glu1117=) rs45554236
NM_000257.4(MYH7):c.3373G>A (p.Glu1125Lys) rs730880904
NM_000257.4(MYH7):c.3446G>C (p.Arg1149Pro) rs768978215
NM_000257.4(MYH7):c.3577C>A (p.Arg1193Ser) rs886039090
NM_000257.4(MYH7):c.3621C>G (p.Ile1207Met) rs529700838
NM_000257.4(MYH7):c.3622G>A (p.Asp1208Asn) rs730880781
NM_000257.4(MYH7):c.3637G>A (p.Val1213Met) rs397516182
NM_000257.4(MYH7):c.3639G>A (p.Val1213=) rs1238904908
NM_000257.4(MYH7):c.3648G>A (p.Lys1216=) rs1555337101
NM_000257.4(MYH7):c.3658_3660del (p.Glu1220del) rs397516190
NM_000257.4(MYH7):c.3682C>T (p.Leu1228=) rs560995739
NM_000257.4(MYH7):c.3770A>G (p.Asn1257Ser) rs574005462
NM_000257.4(MYH7):c.3789G>A (p.Ala1263=) rs137918672
NM_000257.4(MYH7):c.3846C>G (p.Thr1282=) rs948996596
NM_000257.4(MYH7):c.3918C>T (p.Leu1306=) rs144420313
NM_000257.4(MYH7):c.3961_3963delinsAAA (p.Glu1321Lys) rs886038864
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.3982G>A (p.Ala1328Thr) rs372727092
NM_000257.4(MYH7):c.4005G>A (p.Ser1335=) rs144465613
NM_000257.4(MYH7):c.4010G>A (p.Arg1337Gln) rs368575559
NM_000257.4(MYH7):c.4066G>A (p.Glu1356Lys) rs727503246
NM_000257.4(MYH7):c.4083T>G (p.Leu1361=) rs754295295
NM_000257.4(MYH7):c.4130C>T (p.Thr1377Met) rs397516201
NM_000257.4(MYH7):c.4134C>T (p.Asp1378=) rs770630028
NM_000257.4(MYH7):c.4135G>A (p.Ala1379Thr) rs397516202
NM_000257.4(MYH7):c.4145G>A (p.Arg1382Gln) rs727504325
NM_000257.4(MYH7):c.4158C>T (p.Leu1386=) rs886050418
NM_000257.4(MYH7):c.4159G>A (p.Glu1387Lys) rs730880792
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=) rs200852418
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=) rs3729821
NM_000257.4(MYH7):c.427C>T (p.Arg143Trp) rs727503278
NM_000257.4(MYH7):c.453G>A (p.Pro151=) rs777382773
NM_000257.4(MYH7):c.521T>A (p.Ile174Asn) rs1555338750
NM_000257.4(MYH7):c.5245A>C (p.Arg1749=) rs562465062
NM_000257.4(MYH7):c.5253T>C (p.Ala1751=) rs776282574
NM_000257.4(MYH7):c.531-5C>T rs397516243
NM_000257.4(MYH7):c.5326A>G (p.Ser1776Gly) rs369437262
NM_000257.4(MYH7):c.5329G>A (p.Ala1777Thr) rs200939753
NM_000257.4(MYH7):c.538T>A (p.Ser180Thr) rs1555338704
NM_000257.4(MYH7):c.540C>A (p.Ser180=) rs369490861
NM_000257.4(MYH7):c.5412C>G (p.Ala1804=) rs147433856
NM_000257.4(MYH7):c.5421C>T (p.Gly1807=) rs142844109
NM_000257.4(MYH7):c.5481G>A (p.Glu1827=) rs368848344
NM_000257.4(MYH7):c.5484C>T (p.Ala1828=) rs202175645
NM_000257.4(MYH7):c.5499C>T (p.Asn1833=) rs3729831
NM_000257.4(MYH7):c.5559+5G>A rs371177871
NM_000257.4(MYH7):c.5562G>A (p.Thr1854=) rs368706722
NM_000257.4(MYH7):c.5624T>C (p.Val1875Ala) rs886038830
NM_000257.4(MYH7):c.5638C>G (p.Arg1880Gly) rs1057522617
NM_000257.4(MYH7):c.5704G>C (p.Glu1902Gln) rs187073962
NM_000257.4(MYH7):c.5727G>A (p.Arg1909=) rs761750159
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=) rs200728597
NM_000257.4(MYH7):c.5749G>T (p.Val1917Phe) rs397516255
NM_000257.4(MYH7):c.5757G>C (p.Lys1919Asn) rs1343372308
NM_000257.4(MYH7):c.5762G>A (p.Arg1921Gln) rs397516256
NM_000257.4(MYH7):c.5786C>T (p.Thr1929Met) rs730880918
NM_000257.4(MYH7):c.597A>G (p.Ala199=) rs2069541
NM_000257.4(MYH7):c.689T>C (p.Phe230Ser) rs886038844
NM_000257.4(MYH7):c.705C>T (p.Thr235=) rs552415639
NM_000257.4(MYH7):c.709C>T (p.Arg237Trp) rs45516091
NM_000257.4(MYH7):c.710G>A (p.Arg237Gln) rs397516263
NM_000257.4(MYH7):c.714C>T (p.Asn238=) rs202141819
NM_000257.4(MYH7):c.715G>A (p.Asp239Asn) rs397516264
NM_000257.4(MYH7):c.732C>T (p.Phe244=) rs2069542
NM_000257.4(MYH7):c.740T>G (p.Phe247Cys) rs730880922
NM_000257.4(MYH7):c.746G>A (p.Arg249Gln) rs3218713
NM_000257.4(MYH7):c.758G>T (p.Gly253Val) rs730880853
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570
NM_000257.4(MYH7):c.815G>C (p.Arg272Thr) rs1555338578
NM_000257.4(MYH7):c.924C>T (p.Tyr308=) rs762065412
NM_000257.4(MYH7):c.930T>C (p.Tyr310=) rs111626355
NM_000257.4(MYH7):c.954C>G (p.Thr318=) rs773934091
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342
NM_000257.4(MYH7):c.968T>C (p.Ile323Thr) rs397516275
NM_000257.4(MYH7):c.975C>T (p.Asp325=) rs2231124

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