ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.930T>C (p.Tyr310=) rs111626355 0.00091
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643 0.00063
NM_000257.4(MYH7):c.3960G>A (p.Glu1320=) rs147797612 0.00044
NM_000257.4(MYH7):c.4188G>A (p.Arg1396=) rs200852418 0.00032
NM_000257.4(MYH7):c.5412C>G (p.Ala1804=) rs147433856 0.00019
NM_000257.4(MYH7):c.796+7G>A rs369286647 0.00019
NM_000257.4(MYH7):c.5718A>C (p.Ala1906=) rs45523233 0.00016
NM_000257.4(MYH7):c.3861G>C (p.Leu1287=) rs150292548 0.00014
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342 0.00014
NM_000257.4(MYH7):c.3726+6C>T rs377745688 0.00013
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975 0.00012
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354 0.00011
NM_000257.4(MYH7):c.345C>T (p.Tyr115=) rs149439730 0.00011
NM_000257.4(MYH7):c.2184G>A (p.Ala728=) rs148650290 0.00010
NM_000257.4(MYH7):c.2091T>C (p.Gly697=) rs140380523 0.00009
NM_000257.4(MYH7):c.1671G>A (p.Leu557=) rs149386750 0.00007
NM_000257.4(MYH7):c.5397A>G (p.Glu1799=) rs200374977 0.00007
NM_000257.4(MYH7):c.5499C>T (p.Asn1833=) rs3729831 0.00007
NM_000257.4(MYH7):c.1179C>T (p.Ala393=) rs143293426 0.00006
NM_000257.4(MYH7):c.1200C>T (p.Cys400=) rs374806617 0.00006
NM_000257.4(MYH7):c.1322C>T (p.Thr441Met) rs121913653 0.00006
NM_000257.4(MYH7):c.2028T>C (p.Asn676=) rs145564868 0.00006
NM_000257.4(MYH7):c.2145C>T (p.Tyr715=) rs146675572 0.00006
NM_000257.4(MYH7):c.4182C>T (p.Ala1394=) rs765895405 0.00006
NM_000257.4(MYH7):c.78G>A (p.Ala26=) rs746119986 0.00006
NM_000257.4(MYH7):c.1323G>A (p.Thr441=) rs397516096 0.00005
NM_000257.4(MYH7):c.3273C>T (p.Asn1091=) rs200664031 0.00005
NM_000257.4(MYH7):c.502+6A>G rs569044957 0.00005
NM_000257.4(MYH7):c.1266T>C (p.Tyr422=) rs141519877 0.00004
NM_000257.4(MYH7):c.1368C>T (p.Phe456=) rs766216871 0.00004
NM_000257.4(MYH7):c.1482T>C (p.Phe494=) rs587781088 0.00004
NM_000257.4(MYH7):c.28G>C (p.Gly10Arg) rs199577321 0.00004
NM_000257.4(MYH7):c.4077C>T (p.Arg1359=) rs45523835 0.00004
NM_000257.4(MYH7):c.2859C>T (p.Asp953=) rs370800700 0.00003
NM_000257.4(MYH7):c.1518C>T (p.Ile506=) rs397516108 0.00002
NM_000257.4(MYH7):c.210C>T (p.Thr70=) rs774429242 0.00002
NM_000257.4(MYH7):c.530+9A>T rs200925769 0.00002
NM_000257.4(MYH7):c.5730G>A (p.Ala1910=) rs776940948 0.00002
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=) rs200728597 0.00002
NM_000257.4(MYH7):c.1926G>A (p.Ser642=) rs397516126 0.00001
NM_000257.4(MYH7):c.2232G>A (p.Lys744=) rs747848184 0.00001
NM_000257.4(MYH7):c.300G>A (p.Ala100=) rs757141502 0.00001
NM_000257.4(MYH7):c.3682C>T (p.Leu1228=) rs560995739 0.00001
NM_000257.4(MYH7):c.36C>T (p.Ala12=) rs766884630 0.00001
NM_000257.4(MYH7):c.5646C>T (p.Ala1882=) rs730880726 0.00001
NM_000257.4(MYH7):c.1062C>A (p.Gly354=) rs735712
NM_000257.4(MYH7):c.1185G>A (p.Leu395=)
NM_000257.4(MYH7):c.1755C>A (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.1755C>T (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.2280C>T (p.His760=) rs1892666788
NM_000257.4(MYH7):c.3129G>A (p.Lys1043=) rs2138659112
NM_000257.4(MYH7):c.3750G>T (p.Arg1250=)
NM_000257.4(MYH7):c.3789G>A (p.Ala1263=) rs137918672
NM_000257.4(MYH7):c.3829C>A (p.Arg1277=) rs727503248
NM_000257.4(MYH7):c.396G>A (p.Pro132=) rs138932714
NM_000257.4(MYH7):c.396G>T (p.Pro132=) rs138932714
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.5400C>T (p.Ala1800=) rs556490774
NM_000257.4(MYH7):c.5589G>C (p.Arg1863=)
NM_000257.4(MYH7):c.5709G>A (p.Leu1903=) rs988052048
NM_000257.4(MYH7):c.984G>A (p.Glu328=)

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