ClinVar Miner

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

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Gene type:
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Total variants: 39
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HGVS dbSNP
NM_000257.2(MYH7):c.4557C>T (p.Ser1519=) rs150552664
NM_000257.3(MYH7):c.4275C>A (p.Ile1425=) rs57680382
NM_000257.3(MYH7):c.4275C>T (p.Ile1425=) rs57680382
NM_000257.3(MYH7):c.4293C>T (p.Asp1431=) rs45560242
NM_000257.3(MYH7):c.4326G>A (p.Leu1442=) rs727503243
NM_000257.3(MYH7):c.4353+6C>T rs765398896
NM_000257.3(MYH7):c.4362C>G (p.Ala1454=) rs727505281
NM_000257.3(MYH7):c.4371G>A (p.Lys1457=) rs1555336697
NM_000257.3(MYH7):c.4395G>T (p.Ser1465=) rs397516213
NM_000257.3(MYH7):c.4410G>A (p.Ser1470=) rs578166720
NM_000257.3(MYH7):c.4513C>T (p.Leu1505=) rs139928934
NM_000257.3(MYH7):c.4515G>T (p.Leu1505=) rs397516219
NM_000257.3(MYH7):c.4618C>T (p.Leu1540=) rs368734580
NM_000257.3(MYH7):c.4644+3G>A rs397516226
NM_000257.3(MYH7):c.4644+7G>C rs1555336564
NM_000257.3(MYH7):c.4645-16C>T rs778453839
NM_000257.3(MYH7):c.4645-17C>T rs1555336497
NM_000257.3(MYH7):c.4725G>A (p.Lys1575=) rs45476496
NM_000257.3(MYH7):c.4800C>T (p.Ser1600=) rs1057521761
NM_000257.3(MYH7):c.4803G>A (p.Leu1601=) rs397516228
NM_000257.3(MYH7):c.4806C>T (p.Asp1602=) rs142034311
NM_000257.3(MYH7):c.4827C>T (p.Asn1609=) rs587781085
NM_000257.3(MYH7):c.4869T>C (p.Asn1623=) rs1448315071
NM_000257.3(MYH7):c.4911C>T (p.Ala1637=) rs151113658
NM_000257.3(MYH7):c.4941G>A (p.Gln1647=) rs749154313
NM_000257.3(MYH7):c.4953+13A>T rs373509029
NM_000257.3(MYH7):c.4953+17G>A rs376604168
NM_000257.3(MYH7):c.4954-14C>T rs727505070
NM_000257.3(MYH7):c.5019C>T (p.Ile1673=) rs139518691
NM_000257.3(MYH7):c.5070C>G (p.Ala1690=) rs764844610
NM_000257.3(MYH7):c.5115G>A (p.Glu1705=) rs397516239
NM_000257.3(MYH7):c.5158-15C>T rs369453980
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=) rs2754155
NM_000257.4(MYH7):c.4671G>A (p.Lys1557=) rs200601164
NM_000257.4(MYH7):c.4716C>T (p.Ile1572=) rs7140196
NM_000257.4(MYH7):c.4893C>T (p.His1631=) rs369164804
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) rs141122361
NM_000257.4(MYH7):c.4974C>T (p.Asp1658=) rs374289523

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