ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as benign for not specified

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Gene type:
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Total variants: 20
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NM_000257.4(MYH7):c.4290G>T (p.Val1430=) rs372476972
NM_000257.4(MYH7):c.4353+10G>A rs202205780
NM_000257.4(MYH7):c.4353+13T>G rs587781084
NM_000257.4(MYH7):c.4353+17G>A rs45581933
NM_000257.4(MYH7):c.4353+42G>A rs3729822
NM_000257.4(MYH7):c.4354-6G>A rs368078397
NM_000257.4(MYH7):c.4354-7C>T rs370093487
NM_000257.4(MYH7):c.4452C>T (p.Leu1484=) rs61737803
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys) rs3729823
NM_000257.4(MYH7):c.4520-25C>T rs45503601
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=) rs2754155
NM_000257.4(MYH7):c.4618C>T (p.Leu1540=) rs368734580
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.4788G>A (p.Ser1596=) rs146858930
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=) rs142034311
NM_000257.4(MYH7):c.4827C>T (p.Asn1609=) rs587781085
NM_000257.4(MYH7):c.4911C>T (p.Ala1637=) rs151113658
NM_000257.4(MYH7):c.4974C>T (p.Asp1658=) rs374289523
NM_000257.4(MYH7):c.5106G>A (p.Ala1702=) rs3729830

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