ClinVar Miner

List of variants in gene combination MYH8, MYHAS studied for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 156
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002472.3(MYH8):c.1148-234A>G rs2041126 0.87622
NM_002472.3(MYH8):c.714T>C (p.Thr238=) rs8068729 0.86861
NM_002472.3(MYH8):c.2171+45G>A rs2024076 0.63077
NM_002472.3(MYH8):c.4962+149A>G rs9901358 0.60580
NM_002472.3(MYH8):c.3736-158C>G rs3815314 0.56311
NM_002472.3(MYH8):c.5074T>C (p.Trp1692Arg) rs8069834 0.50046
NM_002472.3(MYH8):c.1417-220C>G rs9303258 0.45353
NM_002472.3(MYH8):c.806-139T>C rs4791408 0.43008
NM_002472.3(MYH8):c.806-30T>C rs4791406 0.42084
NM_002472.3(MYH8):c.512-123T>C rs7216301 0.41553
NM_002472.3(MYH8):c.806-41T>C rs4791407 0.40579
NM_002472.3(MYH8):c.1147+94C>T rs11078845 0.38523
NM_002472.3(MYH8):c.1148-230G>A rs2041125 0.37849
NM_002472.3(MYH8):c.1417-131G>A rs12601678 0.36299
NM_002472.3(MYH8):c.1417-111C>T rs12601552 0.36294
NM_002472.3(MYH8):c.2433-166T>C rs60171839 0.34378
NM_002472.3(MYH8):c.-31G>A rs2277648 0.30852
NM_002472.3(MYH8):c.2433-182C>T rs72816704 0.19849
NM_002472.3(MYH8):c.5208C>T (p.Asp1736=) rs33969260 0.17467
NM_002472.3(MYH8):c.5664+223C>T rs34130444 0.17089
NM_002472.3(MYH8):c.4179-309A>G rs58860345 0.10693
NM_002472.3(MYH8):c.5166+178G>C rs79639152 0.09336
NM_002472.3(MYH8):c.1907C>T (p.Ala636Val) rs34693726 0.05120
NM_002472.3(MYH8):c.2016C>T (p.Phe672=) rs12936716 0.05000
NM_002472.3(MYH8):c.1416+131C>T rs72816707 0.04312
NM_002472.3(MYH8):c.3862+174C>T rs71358300 0.04263
NM_002472.3(MYH8):c.*76G>C rs3744551 0.02944
NM_002472.3(MYH8):c.2171+82T>A rs148245264 0.02040
NM_002472.3(MYH8):c.1701G>A (p.Gln567=) rs73275411 0.01912
NM_002472.3(MYH8):c.1148-235C>T rs73977157 0.01684
NM_002472.3(MYH8):c.4233C>T (p.Asn1411=) rs138992963 0.01251
NM_002472.3(MYH8):c.1416+215G>A rs9889712 0.00940
NM_002472.3(MYH8):c.3736-263C>T rs28653529 0.00885
NM_002472.3(MYH8):c.1147+147C>G rs9902705 0.00883
NM_002472.3(MYH8):c.1147+15T>G rs115518385 0.00809
NM_002472.3(MYH8):c.4178+120dup rs201916027 0.00730
NM_002472.3(MYH8):c.-30-104G>C rs79815072 0.00680
NM_002472.3(MYH8):c.3686T>C (p.Met1229Thr) rs35962914 0.00663
NM_002472.3(MYH8):c.4379A>G (p.Lys1460Arg) rs112910113 0.00616
NM_002472.3(MYH8):c.2652A>G (p.Leu884=) rs80168976 0.00605
NM_002472.3(MYH8):c.3757C>T (p.Arg1253Cys) rs34953692 0.00448
NM_002472.3(MYH8):c.805+9C>T rs75468422 0.00426
NM_002472.3(MYH8):c.1632T>C (p.Pro544=) rs144596237 0.00409
NM_002472.3(MYH8):c.*72T>C rs184845947 0.00388
NM_002472.3(MYH8):c.-93T>G rs113848347 0.00379
NM_002472.3(MYH8):c.2432+6A>C rs111692916 0.00351
NM_002472.3(MYH8):c.211-218C>T rs542389644 0.00350
NM_002472.3(MYH8):c.1650C>T (p.Ser550=) rs61730801 0.00347
NM_002472.3(MYH8):c.4740A>C (p.Ala1580=) rs61730806 0.00347
NM_002472.3(MYH8):c.540C>T (p.Thr180=) rs34613390 0.00340
NM_002472.3(MYH8):c.4499C>T (p.Thr1500Met) rs73977155 0.00334
NM_002472.3(MYH8):c.4179-194C>T rs149267669 0.00332
NM_002472.3(MYH8):c.4962+137T>C rs149761278 0.00316
NM_002472.3(MYH8):c.4179-137C>T rs138389156 0.00309
NC_000017.11:g.10390312del rs112236252 0.00300
NM_002472.3(MYH8):c.2174dup (p.Tyr725Ter) rs565515290 0.00261
NM_002472.3(MYH8):c.225G>C (p.Arg75Ser) rs146732664 0.00220
NM_002472.3(MYH8):c.2147T>A (p.Ile716Asn) rs115483891 0.00218
NM_002472.3(MYH8):c.4813G>A (p.Asp1605Asn) rs139344968 0.00209
NM_002472.3(MYH8):c.1209C>A (p.Cys403Ter) rs144321381 0.00124
NM_002472.3(MYH8):c.143C>T (p.Ser48Phe) rs146669648 0.00101
NM_002472.3(MYH8):c.4042G>A (p.Glu1348Lys) rs140562514 0.00083
NM_002472.3(MYH8):c.954G>C (p.Gln318His) rs142606252 0.00081
NM_002472.3(MYH8):c.2274A>G (p.Gln758=) rs145901155 0.00080
NM_002472.3(MYH8):c.430G>C (p.Ala144Pro) rs138262102 0.00065
NM_002472.3(MYH8):c.4878T>C (p.Asn1626=) rs202123184 0.00055
NM_002472.3(MYH8):c.1731G>C (p.Glu577Asp) rs75160168 0.00053
NM_002472.3(MYH8):c.4786G>A (p.Val1596Ile) rs61730807 0.00052
NM_002472.3(MYH8):c.578G>A (p.Arg193His) rs145863180 0.00052
NM_002472.3(MYH8):c.726C>T (p.Asp242=) rs140772576 0.00051
NM_002472.3(MYH8):c.1318C>T (p.Leu440=) rs141899271 0.00049
NM_002472.3(MYH8):c.4784G>C (p.Arg1595Thr) rs145711576 0.00048
NM_002472.3(MYH8):c.4147A>G (p.Ile1383Val) rs138607111 0.00045
NM_002472.3(MYH8):c.5028T>A (p.Ile1676=) rs144886270 0.00041
NM_002472.3(MYH8):c.1470G>A (p.Gln490=) rs142242671 0.00030
NM_002472.3(MYH8):c.59G>A (p.Arg20Gln) rs201580344 0.00026
NM_002472.3(MYH8):c.3874C>T (p.Arg1292Ter) rs150008607 0.00024
NM_002472.3(MYH8):c.277A>G (p.Met93Val) rs144036067 0.00021
NM_002472.3(MYH8):c.2117G>A (p.Arg706His) rs150351713 0.00020
NM_002472.3(MYH8):c.676G>A (p.Ala226Thr) rs140408926 0.00013
NM_002472.3(MYH8):c.741+8T>C rs370684142 0.00013
NM_002472.3(MYH8):c.1815T>A (p.Asn605Lys) rs151091483 0.00012
NM_002472.3(MYH8):c.1905C>T (p.Ser635=) rs377372606 0.00011
NM_002472.3(MYH8):c.2055G>A (p.Gly685=) rs761674430 0.00011
NM_002472.3(MYH8):c.675C>T (p.Ser225=) rs146651214 0.00009
NM_002472.3(MYH8):c.320A>G (p.Asn107Ser) rs139192237 0.00008
NM_002472.3(MYH8):c.1155C>T (p.Asp385=) rs140617211 0.00007
NM_002472.3(MYH8):c.479T>A (p.Ile160Asn) rs760980150 0.00007
NM_002472.3(MYH8):c.-7C>T rs201919885 0.00006
NM_002472.3(MYH8):c.539+1G>A rs149198713 0.00006
NM_002472.3(MYH8):c.1380C>T (p.Ile460=) rs778977499 0.00004
NM_002472.3(MYH8):c.1734C>T (p.Ala578=) rs144464113 0.00004
NM_002472.3(MYH8):c.4470del (p.Tyr1491fs) rs1060499730 0.00004
NM_002472.3(MYH8):c.1833G>A (p.Leu611=) rs202061555 0.00003
NM_002472.3(MYH8):c.2557G>A (p.Ala853Thr) rs1319449107 0.00003
NM_002472.3(MYH8):c.5140G>A (p.Glu1714Lys) rs553069572 0.00003
NM_002472.3(MYH8):c.5789T>G (p.Val1930Gly) rs1346984851 0.00003
NM_002472.3(MYH8):c.4235C>T (p.Ala1412Val) rs750806957 0.00002
NM_002472.3(MYH8):c.1268T>G (p.Val423Gly) rs747960533 0.00001
NM_002472.3(MYH8):c.1663C>T (p.Leu555=) rs1481974689 0.00001
NM_002472.3(MYH8):c.1966-2A>G rs747170484 0.00001
NM_002472.3(MYH8):c.2021G>A (p.Arg674Gln) rs121434590 0.00001
NM_002472.3(MYH8):c.2432+8T>C rs761265244 0.00001
NM_002472.3(MYH8):c.2465G>A (p.Arg822His) rs776002223 0.00001
NM_002472.3(MYH8):c.351C>T (p.Ile117=) rs752219854 0.00001
NM_002472.3(MYH8):c.405G>A (p.Pro135=) rs775704195 0.00001
NM_002472.3(MYH8):c.4089G>A (p.Ala1363=) rs369923394 0.00001
NM_002472.3(MYH8):c.4158A>C (p.Thr1386=) rs543637171 0.00001
NM_002472.3(MYH8):c.4253A>C (p.Glu1418Ala) rs2508027162 0.00001
NM_002472.3(MYH8):c.447G>A (p.Lys149=) rs1202079116 0.00001
NM_002472.3(MYH8):c.4543C>A (p.Leu1515Ile) rs34564342 0.00001
NM_002472.3(MYH8):c.4846A>T (p.Arg1616Ter) rs778961328 0.00001
NM_002472.3(MYH8):c.551G>C (p.Gly184Ala) rs1472258546 0.00001
NM_002472.3(MYH8):c.5743A>G (p.Ile1915Val) rs1216879928 0.00001
NM_002472.3(MYH8):c.629A>G (p.Asp210Gly) rs963790352 0.00001
NM_002472.3(MYH8):c.11G>A (p.Ser4Asn) rs1555558639
NM_002472.3(MYH8):c.1408del (p.Ile470fs) rs1060499728
NM_002472.3(MYH8):c.1475del (p.Phe492fs) rs781085472
NM_002472.3(MYH8):c.1536G>C (p.Thr512=) rs139038037
NM_002472.3(MYH8):c.1548T>C (p.Phe516=) rs2508071671
NM_002472.3(MYH8):c.1667A>C (p.Tyr556Ser) rs1380658768
NM_002472.3(MYH8):c.1755T>C (p.Tyr585=) rs1597402818
NM_002472.3(MYH8):c.1759G>A (p.Gly587Ser)
NM_002472.3(MYH8):c.1966-1G>T rs561214803
NM_002472.3(MYH8):c.1996A>T (p.Arg666Trp)
NM_002472.3(MYH8):c.2128A>T (p.Lys710Ter) rs1060499731
NM_002472.3(MYH8):c.2230G>A (p.Ala744Thr) rs2072193064
NM_002472.3(MYH8):c.2234C>T (p.Ser745Phe) rs1555556803
NM_002472.3(MYH8):c.2433-165GT[11] rs60545187
NM_002472.3(MYH8):c.2433-167_2433-166insCG rs1555556565
NM_002472.3(MYH8):c.2433-167_2433-166insCGTG rs1555556565
NM_002472.3(MYH8):c.2433-167_2433-166insCGTGTG rs1555556565
NM_002472.3(MYH8):c.2691A>G (p.Glu897=) rs1567684537
NM_002472.3(MYH8):c.2746dup (p.Ile916fs) rs1555556193
NM_002472.3(MYH8):c.372C>G (p.Phe124Leu)
NM_002472.3(MYH8):c.3790A>G (p.Thr1264Ala) rs2508037401
NM_002472.3(MYH8):c.3803A>T (p.Glu1268Val) rs2072115603
NM_002472.3(MYH8):c.3860C>T (p.Ala1287Val) rs1268282594
NM_002472.3(MYH8):c.3862+276CA[10] rs59619326
NM_002472.3(MYH8):c.3862+276CA[11] rs59619326
NM_002472.3(MYH8):c.3862+276CA[12] rs59619326
NM_002472.3(MYH8):c.3863-108CA[6] rs746761681
NM_002472.3(MYH8):c.3980A>C (p.Lys1327Thr) rs2508033257
NM_002472.3(MYH8):c.398G>T (p.Trp133Leu) rs483352720
NM_002472.3(MYH8):c.4172A>G (p.Glu1391Gly) rs2508031752
NM_002472.3(MYH8):c.4649C>G (p.Ala1550Gly) rs1344875858
NM_002472.3(MYH8):c.4789G>A (p.Val1597Met)
NM_002472.3(MYH8):c.4962+10T>C rs749401636
NM_002472.3(MYH8):c.5115C>A (p.Ala1705=) rs200890789
NM_002472.3(MYH8):c.5166+179dup rs71365758
NM_002472.3(MYH8):c.5166+229_5166+230dup rs35512526
NM_002472.3(MYH8):c.5166+229dup rs35512526
NM_002472.3(MYH8):c.5166+249_5166+257del rs35512526
NM_002472.3(MYH8):c.5166+257del rs35512526
NM_002472.3(MYH8):c.5623C>T (p.Gln1875Ter) rs1060499727
NM_002472.3(MYH8):c.847G>T (p.Glu283Ter)

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.