ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 84
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HGVS dbSNP
NM_000257.4(MYH7):c.1046T>C (p.Met349Thr) rs121913640
NM_000257.4(MYH7):c.1060G>A (p.Gly354Ser) rs727503270
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.1258-3_1258-2delinsAT rs1555338344
NM_000257.4(MYH7):c.1334C>T (p.Ala445Val) rs752349938
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.1435A>G (p.Asn479Asp) rs1555338261
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.161G>C (p.Arg54Pro) rs397516117
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.1753A>T (p.Ile585Phe) rs886038845
NM_000257.4(MYH7):c.1795del (p.Asp599fs) rs730880936
NM_000257.4(MYH7):c.1805A>G (p.Asn602Ser) rs730880880
NM_000257.4(MYH7):c.1876G>A (p.Gly626Arg) rs876661370
NM_000257.4(MYH7):c.1982A>G (p.Asn661Ser) rs1060501435
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.22G>A (p.Val8Ile) rs754388460
NM_000257.4(MYH7):c.2332G>A (p.Asp778Asn) rs730880895
NM_000257.4(MYH7):c.2348G>A (p.Arg783His) rs397516142
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
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.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.2602G>C (p.Ala868Pro) rs727504356
NM_000257.4(MYH7):c.2618T>C (p.Leu873Pro) rs1555337701
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.2734A>G (p.Lys912Glu) rs730880758
NM_000257.4(MYH7):c.2736G>T (p.Lys912Asn) rs1555337597
NM_000257.4(MYH7):c.2868T>A (p.Asp956Glu) rs140718120
NM_000257.4(MYH7):c.2882T>G (p.Leu961Arg) rs727504374
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.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.3020T>C (p.Leu1007Pro) rs730880763
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.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.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.3770A>G (p.Asn1257Ser) rs574005462
NM_000257.4(MYH7):c.3961_3963delinsAAA (p.Glu1321Lys) rs886038864
NM_000257.4(MYH7):c.3982G>A (p.Ala1328Thr) rs372727092
NM_000257.4(MYH7):c.4010G>A (p.Arg1337Gln) rs368575559
NM_000257.4(MYH7):c.4130C>T (p.Thr1377Met) rs397516201
NM_000257.4(MYH7):c.4145G>A (p.Arg1382Gln) rs727504325
NM_000257.4(MYH7):c.4159G>A (p.Glu1387Lys) rs730880792
NM_000257.4(MYH7):c.427C>T (p.Arg143Trp) rs727503278
NM_000257.4(MYH7):c.521T>A (p.Ile174Asn) rs1555338750
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.5559+5G>A rs371177871
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.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.689T>C (p.Phe230Ser) rs886038844
NM_000257.4(MYH7):c.710G>A (p.Arg237Gln) rs397516263
NM_000257.4(MYH7):c.758G>T (p.Gly253Val) rs730880853
NM_000257.4(MYH7):c.815G>C (p.Arg272Thr) rs1555338578
NM_000257.4(MYH7):c.968T>C (p.Ile323Thr) rs397516275

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