ClinVar Miner

List of variants in gene MYH14 reported as uncertain significance by Invitae

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 221
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.838G>A (p.Val280Ile) rs202246093 0.00028
NM_001145809.2(MYH14):c.2161C>T (p.Arg721Cys) rs373929652 0.00020
NM_001145809.2(MYH14):c.2840G>A (p.Arg947His) rs374883445 0.00018
NM_001145809.2(MYH14):c.4028C>T (p.Ala1343Val) rs374058410 0.00017
NM_001145809.2(MYH14):c.3098C>T (p.Thr1033Met) rs201746408 0.00015
NM_001145809.2(MYH14):c.4666G>A (p.Ala1556Thr) rs758725143 0.00015
NM_001145809.2(MYH14):c.1229G>A (p.Arg410His) rs374720181 0.00013
NM_001145809.2(MYH14):c.2864G>A (p.Arg955Gln) rs576611342 0.00013
NM_001145809.2(MYH14):c.4752C>T (p.Ser1584=) rs377081835 0.00013
NM_001145809.2(MYH14):c.810C>T (p.Phe270=) rs374146214 0.00013
NM_001145809.2(MYH14):c.5876G>A (p.Arg1959Gln) rs200878464 0.00012
NM_001145809.2(MYH14):c.1067C>T (p.Thr356Met) rs151082668 0.00011
NM_001145809.2(MYH14):c.266T>C (p.Leu89Pro) rs988356194 0.00011
NM_001145809.2(MYH14):c.4731C>T (p.Ser1577=) rs766728732 0.00011
NM_001145809.2(MYH14):c.1049G>A (p.Arg350Gln) rs373908919 0.00010
NM_001145809.2(MYH14):c.5990C>T (p.Thr1997Met) rs201986144 0.00010
NM_001145809.2(MYH14):c.2651A>G (p.Tyr884Cys) rs373457292 0.00009
NM_001145809.2(MYH14):c.4378G>A (p.Glu1460Lys) rs746679895 0.00009
NM_001145809.2(MYH14):c.693C>T (p.Pro231=) rs373744231 0.00009
NM_001145809.2(MYH14):c.2162G>A (p.Arg721His) rs377519378 0.00008
NM_001145809.2(MYH14):c.3883C>T (p.Arg1295Trp) rs372367091 0.00007
NM_001145809.2(MYH14):c.1006C>T (p.Arg336Trp) rs371272700 0.00006
NM_001145809.2(MYH14):c.3772C>T (p.Arg1258Cys) rs201727916 0.00006
NM_001145809.2(MYH14):c.5177G>A (p.Arg1726Gln) rs747204998 0.00006
NM_001145809.2(MYH14):c.1265C>G (p.Ala422Gly) rs372324948 0.00005
NM_001145809.2(MYH14):c.230A>C (p.Glu77Ala) rs748365469 0.00005
NM_001145809.2(MYH14):c.2458C>T (p.Arg820Cys) rs767984672 0.00005
NM_001145809.2(MYH14):c.3623C>T (p.Ala1208Val) rs758560911 0.00005
NM_001145809.2(MYH14):c.158G>A (p.Arg53Gln) rs751476713 0.00004
NM_001145809.2(MYH14):c.3260G>A (p.Arg1087Gln) rs370923801 0.00004
NM_001145809.2(MYH14):c.3434G>A (p.Arg1145Gln) rs373207210 0.00004
NM_001145809.2(MYH14):c.3562G>C (p.Glu1188Gln) rs200299854 0.00004
NM_001145809.2(MYH14):c.3595C>T (p.Arg1199Cys) rs371244397 0.00004
NM_001145809.2(MYH14):c.4946G>A (p.Arg1649Gln) rs368076336 0.00004
NM_001145809.2(MYH14):c.5105T>C (p.Val1702Ala) rs775130663 0.00004
NM_001145809.2(MYH14):c.68C>T (p.Ala23Val) rs765789880 0.00004
NM_001145809.2(MYH14):c.1381C>T (p.Arg461Cys) rs752732851 0.00003
NM_001145809.2(MYH14):c.1418G>A (p.Arg473His) rs199812021 0.00003
NM_001145809.2(MYH14):c.1631C>T (p.Pro544Leu) rs371300947 0.00003
NM_001145809.2(MYH14):c.1655C>T (p.Pro552Leu) rs727505282 0.00003
NM_001145809.2(MYH14):c.1789C>T (p.Arg597Trp) rs200843734 0.00003
NM_001145809.2(MYH14):c.2617G>A (p.Ala873Thr) rs376582564 0.00003
NM_001145809.2(MYH14):c.3259C>T (p.Arg1087Trp) rs368372273 0.00003
NM_001145809.2(MYH14):c.4370G>A (p.Arg1457Gln) rs727503224 0.00003
NM_001145809.2(MYH14):c.488G>A (p.Arg163Gln) rs558956312 0.00003
NM_001145809.2(MYH14):c.500G>A (p.Arg167His) rs776632941 0.00003
NM_001145809.2(MYH14):c.548G>A (p.Arg183Gln) rs750639438 0.00003
NM_001145809.2(MYH14):c.566G>A (p.Arg189His) rs766546274 0.00003
NM_001145809.2(MYH14):c.2381T>A (p.Ile794Asn) rs767521890 0.00002
NM_001145809.2(MYH14):c.293G>A (p.Arg98His) rs370947453 0.00002
NM_001145809.2(MYH14):c.4259C>T (p.Ala1420Val) rs727503225 0.00002
NM_001145809.2(MYH14):c.4354C>T (p.Arg1452Trp) rs777626365 0.00002
NM_001145809.2(MYH14):c.4684C>T (p.Arg1562Trp) rs781219181 0.00002
NM_001145809.2(MYH14):c.4694G>A (p.Arg1565Gln) rs374911327 0.00002
NM_001145809.2(MYH14):c.4999C>T (p.Arg1667Trp) rs763195171 0.00002
NM_001145809.2(MYH14):c.5270C>T (p.Ser1757Leu) rs770822041 0.00002
NM_001145809.2(MYH14):c.5441A>G (p.Asn1814Ser) rs758406907 0.00002
NM_001145809.2(MYH14):c.1790G>A (p.Arg597Gln) rs950320701 0.00001
NM_001145809.2(MYH14):c.2086G>A (p.Asp696Asn) rs539256005 0.00001
NM_001145809.2(MYH14):c.2126G>A (p.Arg709Gln) rs766802012 0.00001
NM_001145809.2(MYH14):c.2701C>A (p.Pro901Thr) rs1324093100 0.00001
NM_001145809.2(MYH14):c.2971G>A (p.Glu991Lys) rs367588704 0.00001
NM_001145809.2(MYH14):c.3418C>T (p.Arg1140Trp) rs748538744 0.00001
NM_001145809.2(MYH14):c.3586G>C (p.Glu1196Gln) rs934601408 0.00001
NM_001145809.2(MYH14):c.3880C>G (p.Leu1294Val) rs776801210 0.00001
NM_001145809.2(MYH14):c.38C>T (p.Ala13Val) rs760685746 0.00001
NM_001145809.2(MYH14):c.3974G>A (p.Arg1325Gln) rs201181045 0.00001
NM_001145809.2(MYH14):c.4307G>A (p.Arg1436Gln) rs773527189 0.00001
NM_001145809.2(MYH14):c.4403A>G (p.Glu1468Gly) rs1346824550 0.00001
NM_001145809.2(MYH14):c.4438C>T (p.Arg1480Cys) rs867601827 0.00001
NM_001145809.2(MYH14):c.4444C>T (p.Arg1482Trp) rs779630814 0.00001
NM_001145809.2(MYH14):c.5000G>A (p.Arg1667Gln) rs766573893 0.00001
NM_001145809.2(MYH14):c.5011A>G (p.Thr1671Ala) rs1389680083 0.00001
NM_001145809.2(MYH14):c.520G>A (p.Val174Met) rs373197435 0.00001
NM_001145809.2(MYH14):c.5345+6T>C rs876657874 0.00001
NM_001145809.2(MYH14):c.535G>A (p.Glu179Lys) rs886054588 0.00001
NM_001145809.2(MYH14):c.5534G>A (p.Arg1845Gln) rs201040702 0.00001
NM_001145809.2(MYH14):c.5549G>A (p.Arg1850Gln) rs777220522 0.00001
NM_001145809.2(MYH14):c.5612A>G (p.Lys1871Arg) rs781714533 0.00001
NM_001145809.2(MYH14):c.5858G>A (p.Arg1953Gln) rs754203387 0.00001
NM_001145809.2(MYH14):c.5917G>A (p.Glu1973Lys) rs1383282169 0.00001
NM_001145809.2(MYH14):c.5930G>A (p.Arg1977His) rs771678694 0.00001
NM_001145809.2(MYH14):c.614C>T (p.Thr205Met) rs1413578961 0.00001
NM_001145809.2(MYH14):c.71C>T (p.Ala24Val) rs751017391 0.00001
NM_001145809.2(MYH14):c.851T>C (p.Ile284Thr) rs752106950 0.00001
NM_001145809.2(MYH14):c.1021G>C (p.Gly341Arg)
NM_001145809.2(MYH14):c.1021G>T (p.Gly341Trp)
NM_001145809.2(MYH14):c.110G>C (p.Gly37Ala)
NM_001145809.2(MYH14):c.115G>A (p.Gly39Arg)
NM_001145809.2(MYH14):c.1217A>G (p.Gln406Arg) rs552730148
NM_001145809.2(MYH14):c.1338C>A (p.Phe446Leu)
NM_001145809.2(MYH14):c.1357A>G (p.Lys453Glu) rs2123302097
NM_001145809.2(MYH14):c.1382G>A (p.Arg461His) rs370353590
NM_001145809.2(MYH14):c.1382G>T (p.Arg461Leu) rs370353590
NM_001145809.2(MYH14):c.1390G>T (p.Val464Phe)
NM_001145809.2(MYH14):c.1417C>T (p.Arg473Cys)
NM_001145809.2(MYH14):c.1426C>A (p.Arg476Ser)
NM_001145809.2(MYH14):c.1463C>T (p.Ala488Val)
NM_001145809.2(MYH14):c.1552A>G (p.Met518Val)
NM_001145809.2(MYH14):c.157C>T (p.Arg53Trp)
NM_001145809.2(MYH14):c.158G>C (p.Arg53Pro)
NM_001145809.2(MYH14):c.1609G>A (p.Asp537Asn)
NM_001145809.2(MYH14):c.161G>A (p.Arg54His)
NM_001145809.2(MYH14):c.1647C>G (p.Ile549Met)
NM_001145809.2(MYH14):c.1742C>T (p.Ala581Val)
NM_001145809.2(MYH14):c.1756G>A (p.Gly586Ser)
NM_001145809.2(MYH14):c.1787T>C (p.Leu596Pro)
NM_001145809.2(MYH14):c.181G>C (p.Glu61Gln)
NM_001145809.2(MYH14):c.1843G>T (p.Ala615Ser) rs1322815305
NM_001145809.2(MYH14):c.1847A>G (p.Asn616Ser)
NM_001145809.2(MYH14):c.1891G>A (p.Ala631Thr)
NM_001145809.2(MYH14):c.1895C>G (p.Ala632Gly)
NM_001145809.2(MYH14):c.206C>A (p.Ala69Glu)
NM_001145809.2(MYH14):c.2102G>A (p.Gly701Asp) rs2123333715
NM_001145809.2(MYH14):c.2110C>T (p.Arg704Cys)
NM_001145809.2(MYH14):c.2140C>T (p.Leu714Phe)
NM_001145809.2(MYH14):c.2194A>C (p.Ser732Arg)
NM_001145809.2(MYH14):c.2232+5_2232+8del
NM_001145809.2(MYH14):c.2250_2251inv (p.Arg751Trp)
NM_001145809.2(MYH14):c.2302A>G (p.Ile768Val)
NM_001145809.2(MYH14):c.2375A>G (p.Asn792Ser)
NM_001145809.2(MYH14):c.238_243del (p.Val80_Glu81del)
NM_001145809.2(MYH14):c.2599C>T (p.Arg867Cys) rs753356694
NM_001145809.2(MYH14):c.260G>C (p.Arg87Thr)
NM_001145809.2(MYH14):c.262C>T (p.Arg88Trp)
NM_001145809.2(MYH14):c.2702C>G (p.Pro901Arg)
NM_001145809.2(MYH14):c.2759A>G (p.Gln920Arg)
NM_001145809.2(MYH14):c.275C>T (p.Pro92Leu)
NM_001145809.2(MYH14):c.2816G>A (p.Arg939Gln)
NM_001145809.2(MYH14):c.2826+3G>A
NM_001145809.2(MYH14):c.285G>C (p.Gln95His)
NM_001145809.2(MYH14):c.2872G>A (p.Ala958Thr)
NM_001145809.2(MYH14):c.2920C>T (p.Arg974Cys)
NM_001145809.2(MYH14):c.2968G>A (p.Gly990Ser)
NM_001145809.2(MYH14):c.3068C>T (p.Ala1023Val)
NM_001145809.2(MYH14):c.3280A>G (p.Ile1094Val)
NM_001145809.2(MYH14):c.3293A>C (p.Glu1098Ala)
NM_001145809.2(MYH14):c.3298C>T (p.Arg1100Cys)
NM_001145809.2(MYH14):c.3299G>A (p.Arg1100His)
NM_001145809.2(MYH14):c.3356A>G (p.Asp1119Gly)
NM_001145809.2(MYH14):c.3379_3396dup (p.Glu1127_Gln1132dup) rs1197448518
NM_001145809.2(MYH14):c.3398A>G (p.Gln1133Arg)
NM_001145809.2(MYH14):c.3467+4C>T
NM_001145809.2(MYH14):c.3470C>T (p.Ala1157Val)
NM_001145809.2(MYH14):c.3490C>T (p.Arg1164Trp)
NM_001145809.2(MYH14):c.3515G>A (p.Arg1172Gln)
NM_001145809.2(MYH14):c.3527C>T (p.Ala1176Val) rs2123405169
NM_001145809.2(MYH14):c.3548A>G (p.Glu1183Gly)
NM_001145809.2(MYH14):c.3566G>A (p.Arg1189His)
NM_001145809.2(MYH14):c.3580A>G (p.Lys1194Glu)
NM_001145809.2(MYH14):c.3610G>A (p.Glu1204Lys)
NM_001145809.2(MYH14):c.3734C>T (p.Thr1245Ile)
NM_001145809.2(MYH14):c.3766A>G (p.Arg1256Gly)
NM_001145809.2(MYH14):c.377G>A (p.Arg126Gln)
NM_001145809.2(MYH14):c.3879G>C (p.Glu1293Asp)
NM_001145809.2(MYH14):c.3881T>C (p.Leu1294Pro)
NM_001145809.2(MYH14):c.3907A>G (p.Thr1303Ala)
NM_001145809.2(MYH14):c.3937C>T (p.Arg1313Cys) rs886854359
NM_001145809.2(MYH14):c.3984T>G (p.Asp1328Glu)
NM_001145809.2(MYH14):c.4151A>C (p.Glu1384Ala) rs1286640897
NM_001145809.2(MYH14):c.4166A>G (p.Lys1389Arg)
NM_001145809.2(MYH14):c.4235A>G (p.Glu1412Gly)
NM_001145809.2(MYH14):c.4310G>A (p.Arg1437His)
NM_001145809.2(MYH14):c.4312C>A (p.Gln1438Lys)
NM_001145809.2(MYH14):c.4412A>G (p.Glu1471Gly) rs2123423816
NM_001145809.2(MYH14):c.4432C>T (p.Arg1478Trp) rs199551130
NM_001145809.2(MYH14):c.4442G>A (p.Arg1481His)
NM_001145809.2(MYH14):c.4525C>T (p.Arg1509Cys)
NM_001145809.2(MYH14):c.4526G>A (p.Arg1509His)
NM_001145809.2(MYH14):c.4539+4G>A
NM_001145809.2(MYH14):c.4616G>T (p.Arg1539Leu) rs576482145
NM_001145809.2(MYH14):c.4702C>T (p.Arg1568Trp)
NM_001145809.2(MYH14):c.4714G>A (p.Glu1572Lys) rs776291919
NM_001145809.2(MYH14):c.4735G>A (p.Asp1579Asn)
NM_001145809.2(MYH14):c.4885G>A (p.Ala1629Thr) rs754931173
NM_001145809.2(MYH14):c.4945C>T (p.Arg1649Trp) rs1249048707
NM_001145809.2(MYH14):c.5009G>A (p.Arg1670His)
NM_001145809.2(MYH14):c.5009G>T (p.Arg1670Leu)
NM_001145809.2(MYH14):c.5029C>T (p.Arg1677Cys)
NM_001145809.2(MYH14):c.5030G>A (p.Arg1677His)
NM_001145809.2(MYH14):c.5073G>A (p.Met1691Ile)
NM_001145809.2(MYH14):c.5117G>A (p.Arg1706His)
NM_001145809.2(MYH14):c.5127G>A (p.Gln1709=)
NM_001145809.2(MYH14):c.5167C>T (p.Arg1723Cys)
NM_001145809.2(MYH14):c.5215C>T (p.Arg1739Cys)
NM_001145809.2(MYH14):c.5233G>A (p.Ala1745Thr)
NM_001145809.2(MYH14):c.5245C>T (p.Arg1749Trp)
NM_001145809.2(MYH14):c.5276G>A (p.Arg1759His)
NM_001145809.2(MYH14):c.527C>T (p.Ala176Val) rs2032563527
NM_001145809.2(MYH14):c.5282G>A (p.Arg1761Gln)
NM_001145809.2(MYH14):c.5285G>A (p.Arg1762Gln)
NM_001145809.2(MYH14):c.541G>T (p.Ala181Ser)
NM_001145809.2(MYH14):c.5423G>A (p.Ser1808Asn)
NM_001145809.2(MYH14):c.5473G>C (p.Glu1825Gln)
NM_001145809.2(MYH14):c.5531G>A (p.Gly1844Glu)
NM_001145809.2(MYH14):c.5563C>A (p.Leu1855Ile)
NM_001145809.2(MYH14):c.5564T>G (p.Leu1855Arg)
NM_001145809.2(MYH14):c.5572C>T (p.Arg1858Cys)
NM_001145809.2(MYH14):c.5591C>T (p.Ala1864Val)
NM_001145809.2(MYH14):c.5606G>A (p.Arg1869His)
NM_001145809.2(MYH14):c.5713G>A (p.Ala1905Thr)
NM_001145809.2(MYH14):c.5824C>T (p.Arg1942Trp)
NM_001145809.2(MYH14):c.5857C>T (p.Arg1953Trp)
NM_001145809.2(MYH14):c.5872C>T (p.Arg1958Cys)
NM_001145809.2(MYH14):c.5887C>T (p.Arg1963Cys)
NM_001145809.2(MYH14):c.591-3C>T
NM_001145809.2(MYH14):c.5921C>T (p.Ser1974Phe)
NM_001145809.2(MYH14):c.5960+4T>C rs1555779636
NM_001145809.2(MYH14):c.5963G>T (p.Arg1988Leu)
NM_001145809.2(MYH14):c.5997_6000del (p.Gln2000fs)
NM_001145809.2(MYH14):c.6007del (p.Arg2003fs)
NM_001145809.2(MYH14):c.6013G>A (p.Glu2005Lys) rs765145417
NM_001145809.2(MYH14):c.6041C>T (p.Ala2014Val)
NM_001145809.2(MYH14):c.6071C>G (p.Ser2024Cys) rs1307762363
NM_001145809.2(MYH14):c.646G>A (p.Ala216Thr)
NM_001145809.2(MYH14):c.659C>T (p.Ser220Leu)
NM_001145809.2(MYH14):c.723G>C (p.Glu241Asp)
NM_001145809.2(MYH14):c.727G>C (p.Glu243Gln)
NM_001145809.2(MYH14):c.95G>A (p.Arg32His)
NM_001145809.2(MYH14):c.976G>A (p.Asp326Asn)
NM_001145809.2(MYH14):c.988G>A (p.Glu330Lys)

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