ClinVar Miner

List of variants in gene MYH11 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 136
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002474.3(MYH11):c.2075C>T (p.Ala692Val) rs148893135 0.00028
NM_002474.3(MYH11):c.3209A>G (p.Gln1070Arg) rs147848256 0.00011
NM_002474.3(MYH11):c.3530C>T (p.Thr1177Met) rs201391947 0.00011
NM_002474.3(MYH11):c.3562C>T (p.Arg1188Trp) rs146388001 0.00011
NM_002474.3(MYH11):c.3611C>T (p.Ala1204Val) rs772621139 0.00008
NM_002474.3(MYH11):c.3827C>T (p.Ala1276Val) rs547038802 0.00008
NM_002474.3(MYH11):c.1839G>C (p.Lys613Asn) rs754374723 0.00007
NM_002474.3(MYH11):c.2277C>G (p.Asn759Lys) rs140550319 0.00007
NM_002474.3(MYH11):c.1913C>T (p.Ser638Leu) rs771128441 0.00006
NM_002474.3(MYH11):c.3010C>G (p.Leu1004Val) rs373358736 0.00006
NM_002474.3(MYH11):c.3603C>G (p.His1201Gln) rs199800922 0.00006
NM_002474.3(MYH11):c.508G>A (p.Glu170Lys) rs766315580 0.00006
NM_002474.3(MYH11):c.2496G>C (p.Trp832Cys) rs369196744 0.00005
NM_002474.3(MYH11):c.1768G>A (p.Ala590Thr) rs745516001 0.00004
NM_002474.3(MYH11):c.292G>A (p.Glu98Lys) rs773587055 0.00004
NM_002474.3(MYH11):c.301G>A (p.Val101Met) rs375159635 0.00004
NM_002474.3(MYH11):c.3563G>A (p.Arg1188Gln) rs746615097 0.00004
NM_002474.3(MYH11):c.3817C>T (p.Arg1273Trp) rs142227497 0.00004
NM_002474.3(MYH11):c.769G>A (p.Val257Met) rs112992497 0.00004
NM_002474.3(MYH11):c.935A>G (p.Asn312Ser) rs149964928 0.00004
NM_002474.3(MYH11):c.101G>C (p.Arg34Thr) rs199654191 0.00003
NM_002474.3(MYH11):c.1904C>T (p.Thr635Met) rs745878375 0.00003
NM_002474.3(MYH11):c.2237C>G (p.Ala746Gly) rs778651094 0.00003
NM_002474.3(MYH11):c.2659G>A (p.Glu887Lys) rs201387564 0.00003
NM_002474.3(MYH11):c.2828C>A (p.Ala943Asp) rs763514919 0.00003
NM_002474.3(MYH11):c.3035C>T (p.Thr1012Met) rs373881911 0.00003
NM_002474.3(MYH11):c.3853C>G (p.Leu1285Val) rs1023178766 0.00003
NM_002474.3(MYH11):c.53A>G (p.Lys18Arg) rs756777282 0.00003
NM_002474.3(MYH11):c.94G>A (p.Ala32Thr) rs765295579 0.00003
NM_002474.3(MYH11):c.1037T>C (p.Ile346Thr) rs794728675 0.00002
NM_002474.3(MYH11):c.1300C>T (p.Arg434Cys) rs375276152 0.00002
NM_002474.3(MYH11):c.1879G>A (p.Gly627Ser) rs563865467 0.00002
NM_002474.3(MYH11):c.200A>G (p.Lys67Arg) rs777426396 0.00002
NM_002474.3(MYH11):c.2062G>A (p.Gly688Ser) rs760793367 0.00002
NM_002474.3(MYH11):c.2198C>T (p.Ala733Val) rs776356937 0.00002
NM_002474.3(MYH11):c.2861A>T (p.Asp954Val) rs758880935 0.00002
NM_002474.3(MYH11):c.3125G>A (p.Arg1042Gln) rs771297865 0.00002
NM_002474.3(MYH11):c.3149G>A (p.Arg1050Gln) rs367605434 0.00002
NM_002474.3(MYH11):c.3281C>T (p.Ala1094Val) rs534384552 0.00002
NM_002474.3(MYH11):c.3326C>A (p.Ala1109Asp) rs1046453819 0.00002
NM_002474.3(MYH11):c.3340C>T (p.Arg1114Trp) rs202004234 0.00002
NM_002474.3(MYH11):c.415G>A (p.Val139Ile) rs745609580 0.00002
NM_002474.3(MYH11):c.487C>T (p.Arg163Trp) rs759409339 0.00002
NM_002474.3(MYH11):c.5C>T (p.Ala2Val) rs150600829 0.00002
NM_002474.3(MYH11):c.632C>T (p.Thr211Met) rs557865832 0.00002
NM_002474.3(MYH11):c.988G>A (p.Val330Met) rs368938309 0.00002
NM_002474.3(MYH11):c.119C>T (p.Ser40Leu) rs775927183 0.00001
NM_002474.3(MYH11):c.2099G>A (p.Arg700Gln) rs376758800 0.00001
NM_002474.3(MYH11):c.2288T>C (p.Ile763Thr) rs944017240 0.00001
NM_002474.3(MYH11):c.2297G>A (p.Ser766Asn) rs1050298581 0.00001
NM_002474.3(MYH11):c.2385G>A (p.Ala795=) rs772248675 0.00001
NM_002474.3(MYH11):c.2392C>T (p.Arg798Cys) rs779195096 0.00001
NM_002474.3(MYH11):c.2393G>A (p.Arg798His) rs757602048 0.00001
NM_002474.3(MYH11):c.2476T>C (p.Tyr826His) rs1436181127 0.00001
NM_002474.3(MYH11):c.2600G>A (p.Arg867Gln) rs773993037 0.00001
NM_002474.3(MYH11):c.2812G>A (p.Gly938Ser) rs1227980651 0.00001
NM_002474.3(MYH11):c.281C>T (p.Thr94Met) rs794728681 0.00001
NM_002474.3(MYH11):c.2855T>C (p.Met952Thr) rs372275868 0.00001
NM_002474.3(MYH11):c.3002G>A (p.Arg1001Gln) rs376622843 0.00001
NM_002474.3(MYH11):c.3152A>G (p.Gln1051Arg) rs1555557294 0.00001
NM_002474.3(MYH11):c.3233T>C (p.Ile1078Thr) rs193922629 0.00001
NM_002474.3(MYH11):c.3375G>C (p.Glu1125Asp) rs779019646 0.00001
NM_002474.3(MYH11):c.3397G>A (p.Ala1133Thr) rs148731225 0.00001
NM_002474.3(MYH11):c.3409G>T (p.Ala1137Ser) rs761268562 0.00001
NM_002474.3(MYH11):c.347C>T (p.Thr116Met) rs1220795088 0.00001
NM_002474.3(MYH11):c.3683C>T (p.Thr1228Met) rs755810220 0.00001
NM_002474.3(MYH11):c.3721C>T (p.Arg1241Trp) rs771515309 0.00001
NM_002474.3(MYH11):c.3788A>G (p.Glu1263Gly) rs759729702 0.00001
NM_002474.3(MYH11):c.3844G>A (p.Val1282Ile) rs763285173 0.00001
NM_002474.3(MYH11):c.418G>A (p.Asp140Asn) rs1085307699 0.00001
NM_002474.3(MYH11):c.479C>T (p.Thr160Met) rs794728671 0.00001
NM_002474.3(MYH11):c.488G>A (p.Arg163Gln) rs1060500729 0.00001
NM_002474.3(MYH11):c.98A>G (p.Lys33Arg) rs2043954401 0.00001
NM_001040113.2(MYH11):c.654+1G>A rs770424951
NM_002474.3(MYH11):c.1202T>C (p.Ile401Thr) rs773998062
NM_002474.3(MYH11):c.1313C>A (p.Thr438Asn)
NM_002474.3(MYH11):c.1328C>T (p.Ala443Val) rs2041820377
NM_002474.3(MYH11):c.1354G>A (p.Ala452Thr) rs749264459
NM_002474.3(MYH11):c.1528G>A (p.Asp510Asn) rs112553563
NM_002474.3(MYH11):c.1696C>G (p.Pro566Ala) rs2151272880
NM_002474.3(MYH11):c.1709A>G (p.Lys570Arg)
NM_002474.3(MYH11):c.1715A>G (p.Lys572Arg) rs794728678
NM_002474.3(MYH11):c.1763C>T (p.Ala588Val) rs794728667
NM_002474.3(MYH11):c.2049C>A (p.His683Gln) rs150924100
NM_002474.3(MYH11):c.2067G>C (p.Lys689Asn)
NM_002474.3(MYH11):c.2153G>A (p.Arg718Gln) rs1286713310
NM_002474.3(MYH11):c.2155A>G (p.Ile719Val)
NM_002474.3(MYH11):c.2180+1G>T rs2151260748
NM_002474.3(MYH11):c.2226C>A (p.Asp742Glu)
NM_002474.3(MYH11):c.2320G>A (p.Val774Ile) rs147897132
NM_002474.3(MYH11):c.2375C>T (p.Ala792Val) rs2151259967
NM_002474.3(MYH11):c.2473G>A (p.Ala825Thr)
NM_002474.3(MYH11):c.2482A>C (p.Lys828Gln)
NM_002474.3(MYH11):c.2491A>T (p.Asn831Tyr)
NM_002474.3(MYH11):c.2611G>T (p.Ala871Ser)
NM_002474.3(MYH11):c.2666A>C (p.Lys889Thr) rs1057518502
NM_002474.3(MYH11):c.2685G>C (p.Gln895His)
NM_002474.3(MYH11):c.2704C>G (p.Leu902Val) rs2151250600
NM_002474.3(MYH11):c.2741C>T (p.Ala914Val) rs142128375
NM_002474.3(MYH11):c.2753A>G (p.Gln918Arg)
NM_002474.3(MYH11):c.2781G>A (p.Met927Ile)
NM_002474.3(MYH11):c.2809A>G (p.Arg937Gly) rs2041271138
NM_002474.3(MYH11):c.2848C>G (p.Gln950Glu) rs2041269564
NM_002474.3(MYH11):c.2914G>C (p.Glu972Gln) rs2151248140
NM_002474.3(MYH11):c.291C>G (p.Asn97Lys) rs113363750
NM_002474.3(MYH11):c.2981A>T (p.Asn994Ile) rs1219173895
NM_002474.3(MYH11):c.3115C>G (p.Leu1039Val) rs1223757069
NM_002474.3(MYH11):c.3148C>T (p.Arg1050Ter) rs1270195304
NM_002474.3(MYH11):c.3195C>A (p.Ser1065Arg) rs202136377
NM_002474.3(MYH11):c.3226G>T (p.Ala1076Ser) rs1229749917
NM_002474.3(MYH11):c.3235G>T (p.Ala1079Ser) rs140479999
NM_002474.3(MYH11):c.3274C>G (p.Leu1092Val) rs945042608
NM_002474.3(MYH11):c.3280G>A (p.Ala1094Thr) rs2041152851
NM_002474.3(MYH11):c.3287T>C (p.Leu1096Pro) rs2151244008
NM_002474.3(MYH11):c.3322A>G (p.Asn1108Asp) rs1451959711
NM_002474.3(MYH11):c.33G>C (p.Glu11Asp) rs148562366
NM_002474.3(MYH11):c.3455A>G (p.Lys1152Arg) rs1433294302
NM_002474.3(MYH11):c.3541_3542delinsGC (p.Lys1181Ala) rs1555555783
NM_002474.3(MYH11):c.3563G>T (p.Arg1188Leu) rs746615097
NM_002474.3(MYH11):c.3710C>G (p.Ala1237Gly)
NM_002474.3(MYH11):c.3757AAG[3] (p.Lys1256del) rs730880147
NM_002474.3(MYH11):c.3781G>A (p.Val1261Met) rs1057518389
NM_002474.3(MYH11):c.3805A>G (p.Ser1269Gly) rs200012419
NM_002474.3(MYH11):c.3818G>A (p.Arg1273Gln) rs1473608237
NM_002474.3(MYH11):c.3847_3849del (p.His1283del)
NM_002474.3(MYH11):c.391C>G (p.Leu131Val) rs111247524
NM_002474.3(MYH11):c.404C>T (p.Ser135Leu) rs760445629
NM_002474.3(MYH11):c.59TCA[1] (p.Ile21del) rs1257655501
NM_002474.3(MYH11):c.611G>T (p.Gly204Val)
NM_002474.3(MYH11):c.633G>A (p.Thr211=) rs765225250
NM_002474.3(MYH11):c.668C>T (p.Pro223Leu)
NM_002474.3(MYH11):c.713A>G (p.Asn238Ser)
NM_002474.3(MYH11):c.754G>A (p.Val252Ile) rs772078130
NM_002474.3(MYH11):c.817C>T (p.Arg273Cys) rs1490228863
NM_002474.3(MYH11):c.936T>A (p.Asn312Lys) rs1555565510
NM_002474.3(MYH11):c.963G>C (p.Gln321His) rs794728673

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.