ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by Evolutionary and Medical Genetics Laboratory, Centre for Cellular and Molecular Biology

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Total variants: 18
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HGVS dbSNP
NM_000257.4(MYH7):c.1245G>A (p.Gln415=) rs606231320
NM_000257.4(MYH7):c.1788G>A (p.Lys596=) rs606231325
NM_000257.4(MYH7):c.1802dup (p.Asn602fs) rs672601321
NM_000257.4(MYH7):c.1830G>A (p.Gln610=) rs606231326
NM_000257.4(MYH7):c.1889-27T>A rs606231327
NM_000257.4(MYH7):c.1956+112G>A rs483352953
NM_000257.4(MYH7):c.1956+114G>A rs606231330
NM_000257.4(MYH7):c.2163-18G>A rs606231333
NM_000257.4(MYH7):c.2181A>G (p.Pro727=) rs606231336
NM_000257.4(MYH7):c.2187C>A (p.Ala729=) rs672601320
NM_000257.4(MYH7):c.2469G>T (p.Gly823=) rs606231338
NM_000257.4(MYH7):c.2496C>T (p.Leu832=) rs606231339
NM_000257.4(MYH7):c.2525G>A (p.Ser842Asn) rs397516154
NM_000257.4(MYH7):c.3245+149C>G rs483352965
NM_000257.4(MYH7):c.503-4A>G rs376022200
NM_000257.4(MYH7):c.503-8C>G rs606231313
NM_000257.4(MYH7):c.639+28T>A rs606231314
NM_000257.4(MYH7):c.639+31C>A rs369187721

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