ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance for Cardiomyopathy

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Total variants: 73
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HGVS dbSNP
NM_000257.2(MYH7):c.137T>G (p.Phe46Cys) rs397516104
NM_000257.2(MYH7):c.1514G>T (p.Gly505Val) rs397516109
NM_000257.2(MYH7):c.184G>A (p.Glu62Lys) rs727504416
NM_000257.2(MYH7):c.1970A>T (p.Lys657Met) rs1064793204
NM_000257.2(MYH7):c.2242T>C (p.Ser748Pro) rs876657879
NM_000257.2(MYH7):c.2508C>G (p.Ile836Met) rs772442923
NM_000257.2(MYH7):c.2795T>C (p.Met932Thr) rs202097576
NM_000257.2(MYH7):c.2845G>A (p.Glu949Lys) rs121913629
NM_000257.2(MYH7):c.2846A>T (p.Glu949Val) rs397516175
NM_000257.2(MYH7):c.343T>C (p.Tyr115His) rs397516183
NM_000257.2(MYH7):c.3592G>A (p.Asp1198Asn) rs730880778
NM_000257.2(MYH7):c.3803G>A (p.Arg1268His) rs397516194
NM_000257.2(MYH7):c.4075C>T (p.Arg1359Cys) rs45451303
NM_000257.2(MYH7):c.4210G>A (p.Val1404Met) rs371552806
NM_000257.2(MYH7):c.4259G>A (p.Arg1420Gln) rs397516207
NM_000257.2(MYH7):c.532G>A (p.Gly178Arg) rs730880156
NM_000257.2(MYH7):c.5380C>G (p.Gln1794Glu) rs397516247
NM_000257.3(MYH7):c.1000-7C>T rs200129563
NM_000257.3(MYH7):c.1180G>A (p.Asp394Asn) rs397516093
NM_000257.3(MYH7):c.1193G>A (p.Gly398Glu) rs730880158
NM_000257.3(MYH7):c.1477_1478delAT (p.Met493Valfs) rs727504336
NM_000257.3(MYH7):c.2011C>T (p.Arg671Cys) rs727503263
NM_000257.3(MYH7):c.2069T>C (p.Met690Thr) rs397516128
NM_000257.3(MYH7):c.2714G>C (p.Cys905Ser) rs730880757
NM_000257.3(MYH7):c.2890G>C (p.Val964Leu) rs45496496
NM_000257.3(MYH7):c.3138G>A (p.Met1046Ile) rs201195256
NM_000257.3(MYH7):c.3235C>T (p.Arg1079Trp) rs192722540
NM_000257.3(MYH7):c.3455A>T (p.Glu1152Val) rs397516184
NM_000257.3(MYH7):c.5287G>A (p.Ala1763Thr) rs727504355
NM_000257.3(MYH7):c.5352_5354delGAA (p.Lys1784del) rs730880935
NM_000257.3(MYH7):c.5500G>A (p.Ala1834Thr) rs143362532
NM_000257.3(MYH7):c.5537G>A (p.Arg1846His) rs757803046
NM_000257.3(MYH7):c.5786C>T (p.Thr1929Met) rs730880918
NM_000257.4(MYH7):c.-8G>A
NM_000257.4(MYH7):c.1534G>A (p.Asp512Asn)
NM_000257.4(MYH7):c.161G>T (p.Arg54Leu)
NM_000257.4(MYH7):c.1651A>C (p.Lys551Gln)
NM_000257.4(MYH7):c.2041C>T (p.Pro681Ser)
NM_000257.4(MYH7):c.2213G>A (p.Ser738Asn)
NM_000257.4(MYH7):c.2382T>C (p.Gly794=)
NM_000257.4(MYH7):c.2386C>T (p.Leu796Phe)
NM_000257.4(MYH7):c.2504A>G (p.Lys835Arg)
NM_000257.4(MYH7):c.2525G>C (p.Ser842Thr)
NM_000257.4(MYH7):c.2731A>T (p.Asn911Tyr)
NM_000257.4(MYH7):c.2855G>C (p.Arg952Thr)
NM_000257.4(MYH7):c.2859C>T (p.Asp953=) rs370800700
NM_000257.4(MYH7):c.3035C>A (p.Ala1012Asp) rs779973529
NM_000257.4(MYH7):c.3068C>T (p.Ala1023Val)
NM_000257.4(MYH7):c.3136A>G (p.Met1046Val)
NM_000257.4(MYH7):c.3147G>A (p.Glu1049=)
NM_000257.4(MYH7):c.3149G>A (p.Arg1050Gln)
NM_000257.4(MYH7):c.3154A>G (p.Lys1052Glu)
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr) rs45478699
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354
NM_000257.4(MYH7):c.3422G>A (p.Arg1141Gln)
NM_000257.4(MYH7):c.3451G>C (p.Glu1151Gln)
NM_000257.4(MYH7):c.3460G>A (p.Gly1154Ser)
NM_000257.4(MYH7):c.3483C>G (p.Ile1161Met)
NM_000257.4(MYH7):c.3502G>A (p.Glu1168Lys)
NM_000257.4(MYH7):c.3563C>T (p.Thr1188Ile)
NM_000257.4(MYH7):c.3598G>A (p.Val1200Met)
NM_000257.4(MYH7):c.3783C>G (p.Ser1261Arg)
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4010G>A (p.Arg1337Gln) rs368575559
NM_000257.4(MYH7):c.4045G>A (p.Glu1349Lys)
NM_000257.4(MYH7):c.4063G>A (p.Ala1355Thr)
NM_000257.4(MYH7):c.4084T>C (p.Ser1362Pro)
NM_000257.4(MYH7):c.5386C>T (p.Arg1796Trp)
NM_000257.4(MYH7):c.5588G>A (p.Arg1863Gln) rs45520836
NM_000257.4(MYH7):c.5704G>C (p.Glu1902Gln) rs187073962
NM_000257.4(MYH7):c.5790+9C>G rs1057521992
NM_000257.4(MYH7):c.67C>T (p.Arg23Trp) rs730880828
NM_000257.4(MYH7):c.821T>C (p.Ile274Thr)

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