ClinVar Miner

List of variants in gene MYH6 reported by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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Total variants: 65
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HGVS dbSNP
NM_002471.3(MYH6):c.1007C>G (p.Ala336Gly) rs138572790
NM_002471.3(MYH6):c.1071C>T (p.Ile357=) rs58131640
NM_002471.3(MYH6):c.1122G>A (p.Ala374=) rs148091079
NM_002471.3(MYH6):c.1131C>G (p.Asp377Glu) rs61742472
NM_002471.3(MYH6):c.1131C>T (p.Asp377=) rs61742472
NM_002471.3(MYH6):c.1275C>T (p.Ile425=) rs61742470
NM_002471.3(MYH6):c.1449C>T (p.Asn483=) rs145447555
NM_002471.3(MYH6):c.1935C>T (p.Ser645=) rs142393002
NM_002471.3(MYH6):c.1989C>T (p.Asn663=) rs28730774
NM_002471.3(MYH6):c.2071G>A (p.Val691Ile) rs148915045
NM_002471.3(MYH6):c.2383C>T (p.Arg795Trp) rs202120238
NM_002471.3(MYH6):c.2430-4C>A rs376527296
NM_002471.3(MYH6):c.2538G>A (p.Glu846=) rs730880150
NM_002471.3(MYH6):c.2579G>A (p.Arg860His) rs115845031
NM_002471.3(MYH6):c.2611C>T (p.Arg871Cys) rs376682837
NM_002471.3(MYH6):c.2612G>A (p.Arg871His) rs869025473
NM_002471.3(MYH6):c.2805C>T (p.Asn935=) rs757958461
NM_002471.3(MYH6):c.2806G>T (p.Ala936Ser) rs141704264
NM_002471.3(MYH6):c.2828G>A (p.Arg943His) rs766640013
NM_002471.3(MYH6):c.2928+5G>A rs28730772
NM_002471.3(MYH6):c.2946G>A (p.Glu982=) rs145274612
NM_002471.3(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.3(MYH6):c.3177C>T (p.Gly1059=) rs529676901
NM_002471.3(MYH6):c.3303G>A (p.Val1101=) rs143825034
NM_002471.3(MYH6):c.3343-3delC rs1027186100
NM_002471.3(MYH6):c.3388G>A (p.Ala1130Thr) rs28730771
NM_002471.3(MYH6):c.3480C>T (p.Ser1160=) rs373345984
NM_002471.3(MYH6):c.3569C>T (p.Thr1190Ile) rs759117852
NM_002471.3(MYH6):c.3573C>T (p.Ala1191=) rs727505358
NM_002471.3(MYH6):c.3609C>G (p.Ala1203=) rs149369904
NM_002471.3(MYH6):c.3627C>T (p.Ile1209=) rs147871745
NM_002471.3(MYH6):c.3682C>T (p.Leu1228=) rs1033363939
NM_002471.3(MYH6):c.3844C>G (p.Leu1282Val) rs1425090608
NM_002471.3(MYH6):c.3867G>T (p.Leu1289Phe) rs138127105
NM_002471.3(MYH6):c.3883G>C (p.Glu1295Gln) rs34935550
NM_002471.3(MYH6):c.3903G>A (p.Ser1301=) rs201804323
NM_002471.3(MYH6):c.3927T>C (p.Ser1309=) rs115742584
NM_002471.3(MYH6):c.3979-10C>A rs28730768
NM_002471.3(MYH6):c.3979-7T>C rs535111647
NM_002471.3(MYH6):c.3979-7_3979-4delTCCC rs745326238
NM_002471.3(MYH6):c.3979-7_3979-5delTCC rs397516764
NM_002471.3(MYH6):c.3979-8C>T rs555976716
NM_002471.3(MYH6):c.3979-8_3979-7delinsGC rs727503235
NM_002471.3(MYH6):c.3979-8delC rs193922652
NM_002471.3(MYH6):c.3979-9C>A rs57660219
NM_002471.3(MYH6):c.3979-9C>G rs57660219
NM_002471.3(MYH6):c.4206C>T (p.Ala1402=) rs111638554
NM_002471.3(MYH6):c.4299C>T (p.Asp1433=) rs765006624
NM_002471.3(MYH6):c.4320T>A (p.Ala1440=) rs145566711
NM_002471.3(MYH6):c.4360-7C>T rs58949384
NM_002471.3(MYH6):c.4465G>A (p.Ala1489Thr) rs761539900
NM_002471.3(MYH6):c.4611G>A (p.Val1537=) rs142983918
NM_002471.3(MYH6):c.4782G>A (p.Arg1594=) rs142823394
NM_002471.3(MYH6):c.4899C>T (p.His1633=) rs61742474
NM_002471.3(MYH6):c.4960-9G>A rs557113705
NM_002471.3(MYH6):c.4986G>A (p.Ala1662=) rs77416370
NM_002471.3(MYH6):c.5077G>A (p.Val1693Met) rs373457153
NM_002471.3(MYH6):c.5293G>A (p.Ala1765Thr) rs397516775
NM_002471.3(MYH6):c.5475G>A (p.Glu1825=) rs79143968
NM_002471.3(MYH6):c.5476_5477delinsAA (p.Gly1826Asn) rs878854502
NM_002471.3(MYH6):c.5748G>C (p.Glu1916Asp) rs1566503504
NM_002471.3(MYH6):c.643-5C>T rs199859986
NM_002471.3(MYH6):c.831G>T (p.Gln277His) rs140660481
NM_002471.3(MYH6):c.899-9C>T rs767945761
NM_002471.3(MYH6):c.909G>A (p.Leu303=) rs17091623

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