ClinVar Miner

List of variants in gene MYH7 reported by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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Total variants: 62
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HGVS dbSNP
NM_000257.4(MYH7):c.-8G>A rs45556042
NM_000257.4(MYH7):c.1000-7C>T rs200129563
NM_000257.4(MYH7):c.1063G>A (p.Ala355Thr) rs397516088
NM_000257.4(MYH7):c.1180G>A (p.Asp394Asn) rs397516093
NM_000257.4(MYH7):c.1266T>C (p.Tyr422=) rs141519877
NM_000257.4(MYH7):c.1324C>T (p.Arg442Cys) rs148808089
NM_000257.4(MYH7):c.137T>G (p.Phe46Cys) rs397516104
NM_000257.4(MYH7):c.1514G>T (p.Gly505Val) rs397516109
NM_000257.4(MYH7):c.161G>T (p.Arg54Leu) rs397516117
NM_000257.4(MYH7):c.1651A>C (p.Lys551Gln) rs1566534156
NM_000257.4(MYH7):c.1755C>T (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.184G>A (p.Glu62Lys) rs727504416
NM_000257.4(MYH7):c.1970A>T (p.Lys657Met) rs1064793204
NM_000257.4(MYH7):c.2011C>T (p.Arg671Cys) rs727503263
NM_000257.4(MYH7):c.2069T>C (p.Met690Thr) rs397516128
NM_000257.4(MYH7):c.210C>T (p.Thr70=) rs774429242
NM_000257.4(MYH7):c.2145C>T (p.Tyr715=) rs146675572
NM_000257.4(MYH7):c.2213G>A (p.Ser738Asn) rs730880894
NM_000257.4(MYH7):c.2242T>C (p.Ser748Pro) rs876657879
NM_000257.4(MYH7):c.2332G>A (p.Asp778Asn) rs730880895
NM_000257.4(MYH7):c.2382T>C (p.Gly794=) rs1566531920
NM_000257.4(MYH7):c.2386C>T (p.Leu796Phe) rs1222361739
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975
NM_000257.4(MYH7):c.2504A>G (p.Lys835Arg) rs876657880
NM_000257.4(MYH7):c.2508C>G (p.Ile836Met) rs772442923
NM_000257.4(MYH7):c.2711G>A (p.Arg904His) rs397516165
NM_000257.4(MYH7):c.2714G>C (p.Cys905Ser) rs730880757
NM_000257.4(MYH7):c.2731A>T (p.Asn911Tyr) rs1566530777
NM_000257.4(MYH7):c.2769C>T (p.Asn923=) rs36211716
NM_000257.4(MYH7):c.2770G>A (p.Glu924Lys) rs121913628
NM_000257.4(MYH7):c.2795T>C (p.Met932Thr) rs202097576
NM_000257.4(MYH7):c.2845G>A (p.Glu949Lys) rs121913629
NM_000257.4(MYH7):c.2846A>T (p.Glu949Val) rs397516175
NM_000257.4(MYH7):c.2855G>C (p.Arg952Thr) rs1446444428
NM_000257.4(MYH7):c.2859C>T (p.Asp953=) rs370800700
NM_000257.4(MYH7):c.3136A>G (p.Met1046Val) rs1566529310
NM_000257.4(MYH7):c.3147G>A (p.Glu1049=) rs1216521596
NM_000257.4(MYH7):c.3149G>A (p.Arg1050Gln) rs759579652
NM_000257.4(MYH7):c.3154A>G (p.Lys1052Glu) rs1566529274
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643
NM_000257.4(MYH7):c.3157C>T (p.Arg1053Trp) rs730880903
NM_000257.4(MYH7):c.3273C>T (p.Asn1091=) rs200664031
NM_000257.4(MYH7):c.3337-4dup rs45504498
NM_000257.4(MYH7):c.343T>C (p.Tyr115His) rs397516183
NM_000257.4(MYH7):c.3455A>T (p.Glu1152Val) rs397516184
NM_000257.4(MYH7):c.3803G>A (p.Arg1268His) rs397516194
NM_000257.4(MYH7):c.4045G>A (p.Glu1349Lys) rs1566526272
NM_000257.4(MYH7):c.4075C>T (p.Arg1359Cys) rs45451303
NM_000257.4(MYH7):c.4077C>T (p.Arg1359=) rs45523835
NM_000257.4(MYH7):c.4084T>C (p.Ser1362Pro) rs112771600
NM_000257.4(MYH7):c.4259G>A (p.Arg1420Gln) rs397516207
NM_000257.4(MYH7):c.5287G>A (p.Ala1763Thr) rs727504355
NM_000257.4(MYH7):c.532G>A (p.Gly178Arg) rs730880156
NM_000257.4(MYH7):c.5380C>G (p.Gln1794Glu) rs397516247
NM_000257.4(MYH7):c.5386C>T (p.Arg1796Trp) rs748598020
NM_000257.4(MYH7):c.5500G>A (p.Ala1834Thr) rs143362532
NM_000257.4(MYH7):c.5537G>A (p.Arg1846His) rs757803046
NM_000257.4(MYH7):c.5588G>A (p.Arg1863Gln) rs45520836
NM_000257.4(MYH7):c.5790+9C>G rs1057521992
NM_000257.4(MYH7):c.788T>C (p.Ile263Thr) rs397516269
NM_000257.4(MYH7):c.821T>C (p.Ile274Thr) rs773456019
NM_000257.4(MYH7):c.930T>C (p.Tyr310=) rs111626355

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