ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser) rs745414245
NM_000257.4(MYH7):c.4372C>T (p.Gln1458Ter) rs190577943
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys) rs3729823
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=) rs2754155
NM_000257.4(MYH7):c.4659C>T (p.His1553=) rs570079347
NM_000257.4(MYH7):c.4716C>T (p.Ile1572=) rs7140196
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=) rs142034311
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His) rs373514686
NM_000257.4(MYH7):c.4828G>A (p.Glu1610Lys) rs730880810
NM_000257.4(MYH7):c.4908C>T (p.Ala1636=) rs150241539
NM_000257.4(MYH7):c.5026C>T (p.Arg1676Trp) rs753115999
NM_000257.4(MYH7):c.5106G>A (p.Ala1702=) rs3729830
NM_000257.4(MYH7):c.5208G>C (p.Gln1736His) rs886050416

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