ClinVar Miner

List of variants in gene combination MYH8, MYHAS reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 135
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HGVS dbSNP gnomAD frequency
NM_002472.3(MYH8):c.4042G>A (p.Glu1348Lys) rs140562514 0.00083
NM_002472.3(MYH8):c.4786G>A (p.Val1596Ile) rs61730807 0.00052
NM_002472.3(MYH8):c.4147A>G (p.Ile1383Val) rs138607111 0.00045
NM_002472.3(MYH8):c.59G>A (p.Arg20Gln) rs201580344 0.00026
NM_002472.3(MYH8):c.1067C>T (p.Thr356Ile) rs199851248 0.00024
NM_002472.3(MYH8):c.277A>G (p.Met93Val) rs144036067 0.00021
NM_002472.3(MYH8):c.4994G>A (p.Arg1665Gln) rs199865613 0.00017
NM_002472.3(MYH8):c.1034C>G (p.Thr345Ser) rs147828853 0.00009
NM_002472.3(MYH8):c.254C>T (p.Pro85Leu) rs375714148 0.00009
NM_002472.3(MYH8):c.2600C>G (p.Ala867Gly) rs1011679307 0.00009
NM_002472.3(MYH8):c.4433G>A (p.Arg1478His) rs201586936 0.00009
NM_002472.3(MYH8):c.1583A>G (p.Glu528Gly) rs948334773 0.00008
NM_002472.3(MYH8):c.320A>G (p.Asn107Ser) rs139192237 0.00008
NM_002472.3(MYH8):c.365G>A (p.Gly122Asp) rs200421774 0.00008
NM_002472.3(MYH8):c.3821A>G (p.Asn1274Ser) rs372019710 0.00007
NM_002472.3(MYH8):c.1333C>T (p.Arg445Cys) rs372766209 0.00006
NM_002472.3(MYH8):c.184G>A (p.Val62Ile) rs371294844 0.00006
NM_002472.3(MYH8):c.4313C>G (p.Ser1438Cys) rs781044002 0.00006
NM_002472.3(MYH8):c.4910G>A (p.Arg1637His) rs886052556 0.00006
NM_002472.3(MYH8):c.988G>A (p.Glu330Lys) rs751532878 0.00006
NM_002472.3(MYH8):c.1057T>C (p.Tyr353His) rs774876652 0.00005
NM_002472.3(MYH8):c.2036A>G (p.Asn679Ser) rs768386064 0.00005
NM_002472.3(MYH8):c.161T>C (p.Ile54Thr) rs375148987 0.00004
NM_002472.3(MYH8):c.3684G>C (p.Lys1228Asn) rs368839272 0.00004
NM_002472.3(MYH8):c.601A>G (p.Ile201Val) rs777624162 0.00004
NM_002472.3(MYH8):c.1726G>A (p.Ala576Thr) rs550754244 0.00003
NM_002472.3(MYH8):c.2017G>A (p.Val673Ile) rs142181278 0.00003
NM_002472.3(MYH8):c.2545G>A (p.Glu849Lys) rs774307650 0.00003
NM_002472.3(MYH8):c.4139C>T (p.Thr1380Met) rs565417467 0.00003
NM_002472.3(MYH8):c.4154G>A (p.Arg1385His) rs147143044 0.00003
NM_002472.3(MYH8):c.5140G>A (p.Glu1714Lys) rs553069572 0.00003
NM_002472.3(MYH8):c.959A>T (p.Glu320Val) rs148448600 0.00003
NM_002472.3(MYH8):c.3672G>T (p.Lys1224Asn) rs202177216 0.00002
NM_002472.3(MYH8):c.3811C>T (p.Arg1271Trp) rs761488980 0.00002
NM_002472.3(MYH8):c.4135G>A (p.Glu1379Lys) rs749792075 0.00002
NM_002472.3(MYH8):c.634T>A (p.Ser212Thr) rs567013242 0.00002
NM_002472.3(MYH8):c.100T>C (p.Phe34Leu) rs1217435451 0.00001
NM_002472.3(MYH8):c.1054A>C (p.Ile352Leu) rs759976728 0.00001
NM_002472.3(MYH8):c.1264C>T (p.Gln422Ter) rs371035884 0.00001
NM_002472.3(MYH8):c.1268T>G (p.Val423Gly) rs747960533 0.00001
NM_002472.3(MYH8):c.130G>A (p.Glu44Lys) rs1404447343 0.00001
NM_002472.3(MYH8):c.1334G>A (p.Arg445His) rs764777507 0.00001
NM_002472.3(MYH8):c.1771T>C (p.Tyr591His) rs760777722 0.00001
NM_002472.3(MYH8):c.1937C>T (p.Ser646Phe) rs535957016 0.00001
NM_002472.3(MYH8):c.1988C>T (p.Thr663Met) rs139649943 0.00001
NM_002472.3(MYH8):c.2024G>A (p.Cys675Tyr) rs530070079 0.00001
NM_002472.3(MYH8):c.2087T>C (p.Leu696Pro) rs369392212 0.00001
NM_002472.3(MYH8):c.2396T>A (p.Leu799Gln) rs1368868765 0.00001
NM_002472.3(MYH8):c.259T>C (p.Tyr87His) rs1383825542 0.00001
NM_002472.3(MYH8):c.3949G>A (p.Glu1317Lys) rs1164868270 0.00001
NM_002472.3(MYH8):c.4122G>T (p.Trp1374Cys) rs908787635 0.00001
NM_002472.3(MYH8):c.4268G>A (p.Arg1423Gln) rs768767249 0.00001
NM_002472.3(MYH8):c.4808C>T (p.Thr1603Met) rs775820322 0.00001
NM_002472.3(MYH8):c.5086G>A (p.Glu1696Lys) rs2072059450 0.00001
NM_002472.3(MYH8):c.5629A>G (p.Lys1877Glu) rs762977268 0.00001
NM_002472.3(MYH8):c.5699G>A (p.Arg1900His) rs770787118 0.00001
NM_002472.3(MYH8):c.5728G>A (p.Glu1910Lys) rs755283265 0.00001
NM_002472.3(MYH8):c.907A>G (p.Met303Val) rs752133623 0.00001
NM_002472.3(MYH8):c.1101C>G (p.Phe367Leu) rs2508080172
NM_002472.3(MYH8):c.1139G>T (p.Gly380Val) rs764474712
NM_002472.3(MYH8):c.1256C>T (p.Thr419Ile)
NM_002472.3(MYH8):c.1270T>A (p.Tyr424Asn) rs2508076379
NM_002472.3(MYH8):c.1271A>C (p.Tyr424Ser) rs2072252196
NM_002472.3(MYH8):c.1276G>T (p.Ala426Ser) rs1056398923
NM_002472.3(MYH8):c.1300G>A (p.Val434Ile)
NM_002472.3(MYH8):c.133C>G (p.Pro45Ala)
NM_002472.3(MYH8):c.1403T>C (p.Phe468Ser)
NM_002472.3(MYH8):c.140A>G (p.Glu47Gly) rs1344093428
NM_002472.3(MYH8):c.1498G>C (p.Glu500Gln) rs2508071866
NM_002472.3(MYH8):c.1571T>A (p.Ile524Asn) rs748690722
NM_002472.3(MYH8):c.1573G>A (p.Glu525Lys)
NM_002472.3(MYH8):c.1718A>G (p.Lys573Arg)
NM_002472.3(MYH8):c.1841A>G (p.Lys614Arg)
NM_002472.3(MYH8):c.1843T>C (p.Ser615Pro)
NM_002472.3(MYH8):c.1882G>A (p.Ala628Thr)
NM_002472.3(MYH8):c.1906G>T (p.Ala636Ser)
NM_002472.3(MYH8):c.196A>G (p.Thr66Ala) rs2508097717
NM_002472.3(MYH8):c.1997G>A (p.Arg666Lys)
NM_002472.3(MYH8):c.2011C>T (p.His671Tyr) rs1169981995
NM_002472.3(MYH8):c.2114T>C (p.Ile705Thr)
NM_002472.3(MYH8):c.2152T>C (p.Tyr718His)
NM_002472.3(MYH8):c.2273A>G (p.Gln758Arg) rs945295096
NM_002472.3(MYH8):c.2375A>G (p.Gln792Arg)
NM_002472.3(MYH8):c.2478C>G (p.Asn826Lys)
NM_002472.3(MYH8):c.2498T>G (p.Met833Arg) rs2508053492
NM_002472.3(MYH8):c.2561C>T (p.Thr854Ile)
NM_002472.3(MYH8):c.2599G>A (p.Ala867Thr)
NM_002472.3(MYH8):c.2692G>A (p.Ala898Thr)
NM_002472.3(MYH8):c.2762A>G (p.Lys921Arg)
NM_002472.3(MYH8):c.295C>A (p.Leu99Ile)
NM_002472.3(MYH8):c.3633C>G (p.Asp1211Glu) rs2508040581
NM_002472.3(MYH8):c.3667G>A (p.Glu1223Lys) rs2508040416
NM_002472.3(MYH8):c.3733A>C (p.Lys1245Gln)
NM_002472.3(MYH8):c.3748A>G (p.Lys1250Glu)
NM_002472.3(MYH8):c.3789G>C (p.Lys1263Asn) rs146793402
NM_002472.3(MYH8):c.3844C>T (p.Arg1282Cys)
NM_002472.3(MYH8):c.387C>A (p.Asn129Lys) rs754559937
NM_002472.3(MYH8):c.3893A>G (p.Asp1298Gly) rs1337119789
NM_002472.3(MYH8):c.3973G>A (p.Glu1325Lys)
NM_002472.3(MYH8):c.3977C>T (p.Thr1326Ile) rs1229464291
NM_002472.3(MYH8):c.3991G>A (p.Ala1331Thr)
NM_002472.3(MYH8):c.4002C>G (p.His1334Gln)
NM_002472.3(MYH8):c.4086G>C (p.Arg1362Ser) rs2508032122
NM_002472.3(MYH8):c.4087G>A (p.Ala1363Thr)
NM_002472.3(MYH8):c.4094C>G (p.Ser1365Cys)
NM_002472.3(MYH8):c.4195C>A (p.Arg1399Ser)
NM_002472.3(MYH8):c.4217A>T (p.His1406Leu)
NM_002472.3(MYH8):c.4259C>T (p.Thr1420Met)
NM_002472.3(MYH8):c.4298T>C (p.Leu1433Pro) rs2508026866
NM_002472.3(MYH8):c.4406A>G (p.Glu1469Gly)
NM_002472.3(MYH8):c.4414G>A (p.Ala1472Thr)
NM_002472.3(MYH8):c.4415C>T (p.Ala1472Val)
NM_002472.3(MYH8):c.4467T>G (p.Asn1489Lys)
NM_002472.3(MYH8):c.4502T>G (p.Leu1501Arg)
NM_002472.3(MYH8):c.4540G>T (p.Asp1514Tyr)
NM_002472.3(MYH8):c.4552C>A (p.Gln1518Lys) rs2072078902
NM_002472.3(MYH8):c.4634C>A (p.Ala1545Asp)
NM_002472.3(MYH8):c.4750G>A (p.Glu1584Lys) rs2508021035
NM_002472.3(MYH8):c.4789G>C (p.Val1597Leu) rs369298245
NM_002472.3(MYH8):c.4823T>C (p.Ile1608Thr)
NM_002472.3(MYH8):c.4909C>T (p.Arg1637Cys)
NM_002472.3(MYH8):c.499T>A (p.Phe167Ile) rs2508092877
NM_002472.3(MYH8):c.5064C>G (p.Ile1688Met) rs370605930
NM_002472.3(MYH8):c.5069A>C (p.Glu1690Ala)
NM_002472.3(MYH8):c.5636A>T (p.Lys1879Ile) rs769925803
NM_002472.3(MYH8):c.5771G>A (p.Arg1924Gln)
NM_002472.3(MYH8):c.5800A>G (p.Ile1934Val)
NM_002472.3(MYH8):c.611C>G (p.Thr204Ser) rs2508085484
NM_002472.3(MYH8):c.662A>T (p.Asp221Val) rs2508084768
NM_002472.3(MYH8):c.677C>T (p.Ala226Val)
NM_002472.3(MYH8):c.715G>A (p.Val239Met)
NM_002472.3(MYH8):c.736C>T (p.Arg246Cys) rs768392636
NM_002472.3(MYH8):c.835C>G (p.Gln279Glu) rs1216199703
NM_002472.3(MYH8):c.854G>A (p.Ser285Asn) rs770649624
NM_002472.3(MYH8):c.946G>A (p.Val316Ile)

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