ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_000257.4(MYH7):c.1200C>T (p.Cys400=)
NM_000257.4(MYH7):c.1266T>C (p.Tyr422=) rs141519877
NM_000257.4(MYH7):c.1755C>T (p.Ile585=) rs201860580
NM_000257.4(MYH7):c.1926G>A (p.Ser642=) rs397516126
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.2334C>T (p.Asp778=) rs2069544
NM_000257.4(MYH7):c.240C>T (p.Asn80=) rs200493975
NM_000257.4(MYH7):c.2679+7C>T rs368653983
NM_000257.4(MYH7):c.28G>C (p.Gly10Arg) rs199577321
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=) rs138294643
NM_000257.4(MYH7):c.3273C>T (p.Asn1091=) rs200664031
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354
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.4077C>T (p.Arg1359=) rs45523835
NM_000257.4(MYH7):c.502+6A>G
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=) rs200728597
NM_000257.4(MYH7):c.930T>C (p.Tyr310=) rs111626355
NM_000257.4(MYH7):c.957C>T (p.Thr319=) rs368699342
NM_000257.4(MYH7):c.968T>C (p.Ile323Thr) rs397516275

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