ClinVar Miner

List of variants in gene combination LOC126861896, MYH6 reported as uncertain significance for Hypertrophic cardiomyopathy 14

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Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_002471.4(MYH6):c.4772A>G (p.Asn1591Ser) rs200751434 0.00022
NM_002471.4(MYH6):c.4651-3C>A rs572175190 0.00009
NM_002471.4(MYH6):c.4828C>T (p.Arg1610Cys) rs780726611 0.00009
NM_002471.4(MYH6):c.4727G>A (p.Arg1576Gln) rs771898553 0.00008
NM_002471.4(MYH6):c.4666G>A (p.Glu1556Lys) rs148582147 0.00007
NM_002471.4(MYH6):c.4723G>A (p.Glu1575Lys) rs371067114 0.00006
NM_002471.4(MYH6):c.4747G>A (p.Glu1583Lys) rs397516771 0.00006
NM_002471.4(MYH6):c.4991G>A (p.Arg1664His) rs778287981 0.00006
NM_002471.4(MYH6):c.5095C>T (p.Arg1699Trp) rs766345714 0.00006
NM_002471.4(MYH6):c.5102G>A (p.Arg1701Gln) rs762103586 0.00006
NM_002471.4(MYH6):c.5026G>A (p.Val1676Met) rs773755388 0.00005
NM_002471.4(MYH6):c.4684C>T (p.Arg1562Trp) rs756237624 0.00004
NM_002471.4(MYH6):c.4822C>T (p.Arg1608Cys) rs201683868 0.00004
NM_002471.4(MYH6):c.4993G>A (p.Ala1665Thr) rs374271404 0.00004
NM_002471.4(MYH6):c.4999G>A (p.Asp1667Asn) rs758251388 0.00004
NM_002471.4(MYH6):c.4704C>A (p.Asn1568Lys) rs149771264 0.00003
NM_002471.4(MYH6):c.4721T>A (p.Ile1574Asn) rs199627411 0.00003
NM_002471.4(MYH6):c.4750G>A (p.Glu1584Lys) rs1280321639 0.00003
NM_002471.4(MYH6):c.4768C>A (p.Arg1590Ser) rs544624250 0.00003
NM_002471.4(MYH6):c.4829G>A (p.Arg1610His) rs758792342 0.00003
NM_002471.4(MYH6):c.4985C>T (p.Ala1662Val) rs773445582 0.00003
NM_002471.4(MYH6):c.5101C>T (p.Arg1701Trp) rs765737102 0.00003
NM_002471.4(MYH6):c.5137G>A (p.Glu1713Lys) rs369275573 0.00003
NM_002471.4(MYH6):c.4669G>A (p.Glu1557Lys) rs768283362 0.00002
NM_002471.4(MYH6):c.4685G>A (p.Arg1562Gln) rs371068881 0.00002
NM_002471.4(MYH6):c.4793C>T (p.Ser1598Leu) rs536807961 0.00002
NM_002471.4(MYH6):c.4918G>A (p.Glu1640Lys) rs748924413 0.00002
NM_002471.4(MYH6):c.4981G>A (p.Asp1661Asn) rs771357562 0.00002
NM_002471.4(MYH6):c.5002G>A (p.Asp1668Asn) rs200884672 0.00002
NM_002471.4(MYH6):c.5035C>T (p.Arg1679Cys) rs921540558 0.00002
NM_002471.4(MYH6):c.5036G>A (p.Arg1679His) rs483352719 0.00002
NM_002471.4(MYH6):c.5111C>T (p.Ala1704Val) rs776961989 0.00002
NM_002471.4(MYH6):c.5135G>T (p.Ser1712Ile) rs201383498 0.00002
NM_002471.4(MYH6):c.4700T>G (p.Phe1567Cys) rs750138024 0.00001
NM_002471.4(MYH6):c.4713G>T (p.Lys1571Asn) rs730880151 0.00001
NM_002471.4(MYH6):c.4745A>G (p.Asp1582Gly) rs748264121 0.00001
NM_002471.4(MYH6):c.4769G>A (p.Arg1590His) rs377473560 0.00001
NM_002471.4(MYH6):c.4780C>T (p.Arg1594Trp) rs545198745 0.00001
NM_002471.4(MYH6):c.4781G>A (p.Arg1594Gln) rs146095234 0.00001
NM_002471.4(MYH6):c.4798C>A (p.Gln1600Lys) rs770068575 0.00001
NM_002471.4(MYH6):c.4823G>A (p.Arg1608His) rs747494958 0.00001
NM_002471.4(MYH6):c.4834G>A (p.Glu1612Lys) rs1417882969 0.00001
NM_002471.4(MYH6):c.4874A>G (p.Asn1625Ser) rs776765616 0.00001
NM_002471.4(MYH6):c.4900G>A (p.Ala1634Thr) rs369767936 0.00001
NM_002471.4(MYH6):c.4907G>A (p.Arg1636His) rs746448302 0.00001
NM_002471.4(MYH6):c.4949G>A (p.Ser1650Asn) rs767073355 0.00001
NM_002471.4(MYH6):c.4960-3C>T rs1469231532 0.00001
NM_002471.4(MYH6):c.4990C>T (p.Arg1664Cys) rs780842934 0.00001
NM_002471.4(MYH6):c.5033G>A (p.Arg1678Gln) rs141195890 0.00001
NM_002471.4(MYH6):c.5071C>T (p.Arg1691Cys) rs745747137 0.00001
NM_002471.4(MYH6):c.5072G>A (p.Arg1691His) rs727504502 0.00001
NM_002471.4(MYH6):c.5089A>G (p.Thr1697Ala) rs727503233 0.00001
NM_002471.4(MYH6):c.4667A>G (p.Glu1556Gly)
NM_002471.4(MYH6):c.4673G>T (p.Gly1558Val) rs1276524636
NM_002471.4(MYH6):c.4685G>T (p.Arg1562Leu) rs371068881
NM_002471.4(MYH6):c.4687G>T (p.Ala1563Ser)
NM_002471.4(MYH6):c.4691A>G (p.Gln1564Arg) rs1195354569
NM_002471.4(MYH6):c.4708A>G (p.Ile1570Val) rs1258827113
NM_002471.4(MYH6):c.4726C>T (p.Arg1576Trp)
NM_002471.4(MYH6):c.4735G>A (p.Ala1579Thr) rs1333346577
NM_002471.4(MYH6):c.4755G>A (p.Met1585Ile) rs1060501427
NM_002471.4(MYH6):c.4759C>T (p.Gln1587Ter)
NM_002471.4(MYH6):c.4763C>G (p.Ala1588Gly)
NM_002471.4(MYH6):c.4763C>T (p.Ala1588Val)
NM_002471.4(MYH6):c.4791C>A (p.Asp1597Glu) rs761627508
NM_002471.4(MYH6):c.4792_4793delinsCG (p.Ser1598Arg) rs2138585182
NM_002471.4(MYH6):c.4804T>G (p.Ser1602Ala)
NM_002471.4(MYH6):c.4812T>G (p.Asp1604Glu) rs201667127
NM_002471.4(MYH6):c.4817A>T (p.Glu1606Val)
NM_002471.4(MYH6):c.4820C>T (p.Thr1607Ile)
NM_002471.4(MYH6):c.4821_4822del (p.Arg1608fs) rs764543612
NM_002471.4(MYH6):c.4846G>C (p.Val1616Leu) rs372923261
NM_002471.4(MYH6):c.4850A>C (p.Lys1617Thr)
NM_002471.4(MYH6):c.4854G>C (p.Lys1618Asn) rs766153681
NM_002471.4(MYH6):c.4884G>T (p.Glu1628Asp) rs1891022943
NM_002471.4(MYH6):c.4885A>G (p.Ile1629Val)
NM_002471.4(MYH6):c.4914_4915inv (p.Ala1639Thr)
NM_002471.4(MYH6):c.4920G>C (p.Glu1640Asp) rs777323881
NM_002471.4(MYH6):c.4922C>T (p.Ala1641Val)
NM_002471.4(MYH6):c.4925A>C (p.Gln1642Pro) rs1487346307
NM_002471.4(MYH6):c.4928A>C (p.Lys1643Thr)
NM_002471.4(MYH6):c.4930C>G (p.Gln1644Glu)
NM_002471.4(MYH6):c.4941C>G (p.Ser1647Arg) rs2138584877
NM_002471.4(MYH6):c.4945C>T (p.Gln1649Ter)
NM_002471.4(MYH6):c.4948A>G (p.Ser1650Gly) rs1595049396
NM_002471.4(MYH6):c.4960G>A (p.Asp1654Asn)
NM_002471.4(MYH6):c.5002G>C (p.Asp1668His) rs200884672
NM_002471.4(MYH6):c.5045T>C (p.Leu1682Pro) rs2138584230
NM_002471.4(MYH6):c.5046dup (p.Leu1683fs)
NM_002471.4(MYH6):c.5062G>A (p.Glu1688Lys) rs727504739
NM_002471.4(MYH6):c.5069T>G (p.Leu1690Arg) rs1421693475
NM_002471.4(MYH6):c.5128G>A (p.Glu1710Lys) rs1595048900
NM_002471.4(MYH6):c.5130G>T (p.Glu1710Asp)
NM_002471.4(MYH6):c.5137G>C (p.Glu1713Gln) rs369275573
NM_002471.4(MYH6):c.5140C>T (p.Arg1714Trp) rs140651265
NM_002471.4(MYH6):c.5141G>A (p.Arg1714Gln)
NM_002471.4(MYH6):c.5161C>T (p.Gln1721Ter) rs2138583963

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