ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance for Cardiomyopathy

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Total variants: 46
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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.4423C>T (p.Arg1475Cys) rs139646545 0.00009
NM_000257.4(MYH7):c.4283T>C (p.Leu1428Ser) rs727503244 0.00006
NM_000257.4(MYH7):c.4353+5G>A rs200436876 0.00006
NM_000257.4(MYH7):c.4363G>A (p.Glu1455Lys) rs876661373 0.00006
NM_000257.4(MYH7):c.4294G>A (p.Val1432Ile) rs144200285 0.00005
NM_000257.4(MYH7):c.4348G>A (p.Asp1450Asn) rs397516211 0.00004
NM_000257.4(MYH7):c.4499G>A (p.Arg1500Gln) rs121913647 0.00002
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=) rs150552664 0.00002
NM_000257.4(MYH7):c.4558G>A (p.Gly1520Arg) rs763683589 0.00002
NM_000257.4(MYH7):c.4301G>A (p.Arg1434His) rs780625785 0.00001
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser) rs745414245 0.00001
NM_000257.4(MYH7):c.4343A>T (p.Asn1448Ile) rs753484341 0.00001
NM_000257.4(MYH7):c.4353+6C>T rs765398896 0.00001
NM_000257.4(MYH7):c.4354-5G>A rs950409210 0.00001
NM_000257.4(MYH7):c.4390C>T (p.Gln1464Ter) rs754829218 0.00001
NM_000257.4(MYH7):c.4394C>T (p.Ser1465Leu) rs1033511138 0.00001
NM_000257.4(MYH7):c.4459G>A (p.Ala1487Thr) rs766909770 0.00001
NM_000257.4(MYH7):c.4481A>T (p.His1494Leu) rs727505329 0.00001
NM_000257.4(MYH7):c.4489A>T (p.Thr1497Ser) rs928227757 0.00001
NM_000257.4(MYH7):c.4525A>C (p.Ile1509Leu) rs397516221 0.00001
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225 0.00001
NM_000257.4(MYH7):c.4606G>A (p.Glu1536Lys) rs779315151 0.00001
NM_000257.4(MYH7):c.4300C>T (p.Arg1434Cys) rs730880800
NM_000257.4(MYH7):c.4347C>G (p.Phe1449Leu) rs182311329
NM_000257.4(MYH7):c.4360G>A (p.Ala1454Thr) rs1358268382
NM_000257.4(MYH7):c.4384G>A (p.Glu1462Lys) rs1892258263
NM_000257.4(MYH7):c.4396G>T (p.Glu1466Ter)
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val) rs397516214
NM_000257.4(MYH7):c.4411C>T (p.Gln1471Ter) rs397516216
NM_000257.4(MYH7):c.4427C>T (p.Ser1476Phe) rs1566525169
NM_000257.4(MYH7):c.4436C>T (p.Thr1479Ile) rs397516217
NM_000257.4(MYH7):c.4454A>G (p.Lys1485Arg) rs1566525134
NM_000257.4(MYH7):c.4458C>A (p.Asn1486Lys) rs571704020
NM_000257.4(MYH7):c.4463A>G (p.Tyr1488Cys) rs948329167
NM_000257.4(MYH7):c.4483C>G (p.Leu1495Val) rs1892252122
NM_000257.4(MYH7):c.4511A>C (p.Asn1504Thr) rs1892250074
NM_000257.4(MYH7):c.4524G>C (p.Glu1508Asp) rs1033543834
NM_000257.4(MYH7):c.4527C>G (p.Ile1509Met) rs781223723
NM_000257.4(MYH7):c.4537A>T (p.Thr1513Ser) rs397516222
NM_000257.4(MYH7):c.4541A>G (p.Glu1514Gly) rs1351712658
NM_000257.4(MYH7):c.4565C>T (p.Thr1522Ile) rs2138644446
NM_000257.4(MYH7):c.4568T>C (p.Ile1523Thr) rs1892237828
NM_000257.4(MYH7):c.4584_4585delinsAT (p.Val1529Phe) rs1892237017
NM_000257.4(MYH7):c.4628C>T (p.Ala1543Val) rs1892235051
NM_000257.4(MYH7):c.4643A>T (p.Glu1548Val) rs730880804

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