ClinVar Miner

List of variants in gene combination MHRT, MYH7 studied for not provided

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Total variants: 107
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.4644+80C>T rs3729828 0.43652
NM_000257.4(MYH7):c.4644+190C>T rs3729829 0.43603
NM_000257.4(MYH7):c.4645-173C>T rs7140721 0.43561
NM_000257.4(MYH7):c.4520-63G>A rs3729825 0.19597
NM_000257.4(MYH7):c.4353+42G>A rs3729822 0.06369
NM_000257.4(MYH7):c.4644+57C>G rs3729827 0.02808
NM_000257.4(MYH7):c.4644+113G>A rs7146601 0.01490
NM_000257.4(MYH7):c.4645-220C>T rs7140743 0.01448
NM_000257.4(MYH7):c.4353+17G>A rs45581933 0.01445
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys) rs3729823 0.00861
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=) rs2754155 0.00831
NM_000257.4(MYH7):c.4520-25C>T rs45503601 0.00787
NM_000257.4(MYH7):c.4645-273T>C rs146641667 0.00561
NM_000257.4(MYH7):c.4354-61A>T rs559916092 0.00559
NM_000257.4(MYH7):c.4644+24G>T rs3729826 0.00312
NM_000257.4(MYH7):c.4520-79G>A rs147064810 0.00305
NM_000257.4(MYH7):c.4452C>T (p.Leu1484=) rs61737803 0.00275
NM_000257.4(MYH7):c.4353+10G>A rs202205780 0.00274
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.4423C>T (p.Arg1475Cys) rs139646545 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.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.4347C>T (p.Phe1449=) rs182311329 0.00005
NM_000257.4(MYH7):c.4348G>A (p.Asp1450Asn) rs397516211 0.00004
NM_000257.4(MYH7):c.4353+23A>G rs533030007 0.00004
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.4354-7C>G rs370093487 0.00002
NM_000257.4(MYH7):c.4389G>A (p.Ser1463=) rs781203524 0.00002
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.4641C>T (p.Ala1547=) rs376854724 0.00002
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser) rs745414245 0.00001
NM_000257.4(MYH7):c.4326G>A (p.Leu1442=) rs727503243 0.00001
NM_000257.4(MYH7):c.4343A>T (p.Asn1448Ile) rs753484341 0.00001
NM_000257.4(MYH7):c.4353+20C>T rs199912646 0.00001
NM_000257.4(MYH7):c.4353+6C>T rs765398896 0.00001
NM_000257.4(MYH7):c.4388C>T (p.Ser1463Leu) rs890401818 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.4487A>C (p.Glu1496Ala) rs397516218 0.00001
NM_000257.4(MYH7):c.4489A>T (p.Thr1497Ser) rs928227757 0.00001
NM_000257.4(MYH7):c.4520-3C>T rs549509054 0.00001
NM_000257.4(MYH7):c.4587C>A (p.Val1529=) rs148054271 0.00001
NM_000257.3(MYH7):c.4522_4524del rs397516220
NM_000257.4(MYH7):c.4270G>A (p.Glu1424Lys) rs730880798
NM_000257.4(MYH7):c.4275C>A (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4276G>A (p.Glu1426Lys) rs397516208
NM_000257.4(MYH7):c.4285A>T (p.Met1429Leu) rs1595075282
NM_000257.4(MYH7):c.4286T>C (p.Met1429Thr)
NM_000257.4(MYH7):c.4300C>T (p.Arg1434Cys) rs730880800
NM_000257.4(MYH7):c.4322_4324dup (p.Ala1441_Leu1442insPro) rs2138646436
NM_000257.4(MYH7):c.4327G>A (p.Asp1443Asn) rs2138646412
NM_000257.4(MYH7):c.4327G>C (p.Asp1443His) rs2138646412
NM_000257.4(MYH7):c.4332G>A (p.Lys1444=) rs1064797183
NM_000257.4(MYH7):c.4347C>G (p.Phe1449Leu) rs182311329
NM_000257.4(MYH7):c.4353+9T>G rs2138646292
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val) rs397516214
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys) rs876657884
NM_000257.4(MYH7):c.4411C>T (p.Gln1471Ter) rs397516216
NM_000257.4(MYH7):c.4414_4416del (p.Lys1472del) rs1555336672
NM_000257.4(MYH7):c.4436C>T (p.Thr1479Ile) rs397516217
NM_000257.4(MYH7):c.4441C>T (p.Leu1481Phe) rs767666398
NM_000257.4(MYH7):c.4449A>G (p.Lys1483=) rs558413189
NM_000257.4(MYH7):c.4457A>G (p.Asn1486Ser) rs2138645374
NM_000257.4(MYH7):c.4467G>C (p.Glu1489Asp) rs1892253421
NM_000257.4(MYH7):c.4470G>C (p.Glu1490Asp) rs730880911
NM_000257.4(MYH7):c.4475T>C (p.Leu1492Pro) rs1892252730
NM_000257.4(MYH7):c.4477G>T (p.Glu1493Ter) rs2138645254
NM_000257.4(MYH7):c.4493T>A (p.Phe1498Tyr)
NM_000257.4(MYH7):c.4493_4494delinsAT (p.Phe1498Tyr) rs2138645175
NM_000257.4(MYH7):c.4498C>T (p.Arg1500Trp) rs45544633
NM_000257.4(MYH7):c.4499G>C (p.Arg1500Pro) rs121913647
NM_000257.4(MYH7):c.4506C>A (p.Asn1502Lys)
NM_000257.4(MYH7):c.4515G>T (p.Leu1505=) rs397516219
NM_000257.4(MYH7):c.4519+9G>C rs2138645065
NM_000257.4(MYH7):c.4520-38C>G rs1361469373
NM_000257.4(MYH7):c.4520-42A>T rs2138644761
NM_000257.4(MYH7):c.4532A>C (p.Asp1511Ala) rs730880802
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.4547T>A (p.Leu1516Ter)
NM_000257.4(MYH7):c.4555A>G (p.Ser1519Gly)
NM_000257.4(MYH7):c.4563G>C (p.Lys1521Asn)
NM_000257.4(MYH7):c.4571A>C (p.His1524Pro) rs767148171
NM_000257.4(MYH7):c.4577T>C (p.Leu1526Pro) rs1892237346
NM_000257.4(MYH7):c.4581G>A (p.Glu1527=) rs2138644369
NM_000257.4(MYH7):c.4588C>G (p.Arg1530Gly) rs397516225
NM_000257.4(MYH7):c.4589G>A (p.Arg1530Gln) rs730880803
NM_000257.4(MYH7):c.4606G>T (p.Glu1536Ter) rs779315151
NM_000257.4(MYH7):c.4616A>G (p.Glu1539Gly) rs1446214564
NM_000257.4(MYH7):c.4622A>C (p.Gln1541Pro) rs587779389
NM_000257.4(MYH7):c.4643A>C (p.Glu1548Ala) rs730880804
NM_000257.4(MYH7):c.4644+1del rs2138644180
NM_000257.4(MYH7):c.4644+2del rs2138644167
NM_000257.4(MYH7):c.4644+5G>C rs730880797
NM_000257.4(MYH7):c.4645-196C>T rs76614781

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