ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as likely benign for Cardiomyopathy

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101 0.00024
NM_000257.4(MYH7):c.4513C>T (p.Leu1505=) rs139928934 0.00014
NM_000257.4(MYH7):c.4354-6G>A rs368078397 0.00009
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242 0.00008
NM_000257.4(MYH7):c.4618C>T (p.Leu1540=) rs368734580 0.00007
NM_000257.4(MYH7):c.4290G>T (p.Val1430=) rs372476972 0.00005
NM_000257.4(MYH7):c.4347C>T (p.Phe1449=) rs182311329 0.00005
NM_000257.4(MYH7):c.4519+6C>T rs370779504 0.00005
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720 0.00004
NM_000257.4(MYH7):c.4458C>T (p.Asn1486=) rs571704020 0.00004
NM_000257.4(MYH7):c.4520-15G>A rs200886528 0.00004
NM_000257.4(MYH7):c.4605C>T (p.Ala1535=) rs746261895 0.00004
NM_000257.4(MYH7):c.4389G>A (p.Ser1463=) rs781203524 0.00002
NM_000257.4(MYH7):c.4520-11T>C rs778736821 0.00002
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=) rs150552664 0.00002
NM_000257.4(MYH7):c.4641C>T (p.Ala1547=) rs376854724 0.00002
NM_000257.4(MYH7):c.4326G>A (p.Leu1442=) rs727503243 0.00001
NM_000257.4(MYH7):c.4354-15C>T rs1175603569 0.00001
NM_000257.4(MYH7):c.4520-3C>T rs549509054 0.00001
NM_000257.4(MYH7):c.4530C>T (p.Ser1510=) rs755246527 0.00001
NM_000257.4(MYH7):c.4572T>C (p.His1524=) rs1246893810 0.00001
NM_000257.4(MYH7):c.4587C>A (p.Val1529=) rs148054271 0.00001
NM_000257.4(MYH7):c.4644+3G>A rs397516226 0.00001
NM_000257.4(MYH7):c.4275C>A (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4275C>T (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4278G>A (p.Glu1426=) rs763144369
NM_000257.4(MYH7):c.4302C>T (p.Arg1434=) rs900405502
NM_000257.4(MYH7):c.4308T>C (p.Asn1436=) rs1892272545
NM_000257.4(MYH7):c.4335G>A (p.Lys1445=) rs1892271096
NM_000257.4(MYH7):c.4350C>T (p.Asp1450=) rs1892270412
NM_000257.4(MYH7):c.4354-10C>T rs543141581
NM_000257.4(MYH7):c.4354-7C>T rs370093487
NM_000257.4(MYH7):c.4359G>A (p.Leu1453=) rs1892260171
NM_000257.4(MYH7):c.4395G>A (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4395G>T (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4419G>A (p.Glu1473=) rs1892255907
NM_000257.4(MYH7):c.4434C>T (p.Ser1478=)
NM_000257.4(MYH7):c.4449A>G (p.Lys1483=) rs558413189
NM_000257.4(MYH7):c.4479A>G (p.Glu1493=) rs1892252462
NM_000257.4(MYH7):c.4488G>A (p.Glu1496=) rs1892251841
NM_000257.4(MYH7):c.4498C>A (p.Arg1500=) rs45544633
NM_000257.4(MYH7):c.4515G>A (p.Leu1505=) rs397516219
NM_000257.4(MYH7):c.4515G>T (p.Leu1505=) rs397516219
NM_000257.4(MYH7):c.4521G>A (p.Glu1507=) rs543139794
NM_000257.4(MYH7):c.4542G>A (p.Glu1514=) rs750753882
NM_000257.4(MYH7):c.4551T>C (p.Gly1517=) rs1892238660
NM_000257.4(MYH7):c.4593G>A (p.Lys1531=) rs747037455
NM_000257.4(MYH7):c.4617G>A (p.Glu1539=) rs2138644273
NM_000257.4(MYH7):c.4629C>T (p.Ala1543=) rs1892234964

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