ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
Download table as spreadsheet
HGVS dbSNP
NM_002471.3(MYH6):c.1007C>G (p.Ala336Gly) rs138572790
NM_002471.3(MYH6):c.1935C>T (p.Ser645=) rs142393002
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.2575G>T (p.Gly859Trp) rs369274077
NM_002471.3(MYH6):c.2612G>A (p.Arg871His) rs869025473
NM_002471.3(MYH6):c.2828G>A (p.Arg943His) rs766640013
NM_002471.3(MYH6):c.3154C>T (p.Arg1052Ter) rs532606047
NM_002471.3(MYH6):c.3177C>T (p.Gly1059=) rs529676901
NM_002471.3(MYH6):c.3343-3del rs1027186100
NM_002471.3(MYH6):c.3569C>T (p.Thr1190Ile) rs759117852
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.3979-10C>A rs28730768
NM_002471.3(MYH6):c.3979-7T>C rs535111647
NM_002471.3(MYH6):c.3979-7_3979-4del rs745326238
NM_002471.3(MYH6):c.3979-7_3979-5del rs397516764
NM_002471.3(MYH6):c.3979-7_3979-6del rs796313537
NM_002471.3(MYH6):c.3979-8C>T rs555976716
NM_002471.3(MYH6):c.3979-8del rs193922652
NM_002471.3(MYH6):c.3979-9C>A rs57660219
NM_002471.3(MYH6):c.3979-9C>G rs57660219
NM_002471.3(MYH6):c.3979-9_3979-8del rs193922652
NM_002471.3(MYH6):c.4299C>T (p.Asp1433=) rs765006624
NM_002471.3(MYH6):c.4359+10G>A rs368183862
NM_002471.3(MYH6):c.4465G>A (p.Ala1489Thr) rs761539900
NM_002471.3(MYH6):c.4665C>T (p.His1555=) rs373888186
NM_002471.3(MYH6):c.5077G>A (p.Val1693Met) rs373457153
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.899-9C>T rs767945761
NM_002471.4(MYH6):c.1071C>T (p.Ile357=) rs58131640
NM_002471.4(MYH6):c.1122G>A (p.Ala374=) rs148091079
NM_002471.4(MYH6):c.1131C>G (p.Asp377Glu) rs61742472
NM_002471.4(MYH6):c.1131C>T (p.Asp377=) rs61742472
NM_002471.4(MYH6):c.1132G>A (p.Gly378Ser) rs148962966
NM_002471.4(MYH6):c.1200G>A (p.Leu400=)
NM_002471.4(MYH6):c.1275C>T (p.Ile425=) rs61742470
NM_002471.4(MYH6):c.1449C>T (p.Asn483=) rs145447555
NM_002471.4(MYH6):c.1892-10C>T
NM_002471.4(MYH6):c.1989C>T (p.Asn663=) rs28730774
NM_002471.4(MYH6):c.2071G>A (p.Val691Ile) rs148915045
NM_002471.4(MYH6):c.2579G>A (p.Arg860His) rs115845031
NM_002471.4(MYH6):c.2611C>T (p.Arg871Cys) rs376682837
NM_002471.4(MYH6):c.2614C>T (p.Arg872Cys) rs201193346
NM_002471.4(MYH6):c.2805C>T (p.Asn935=) rs757958461
NM_002471.4(MYH6):c.2806G>T (p.Ala936Ser) rs141704264
NM_002471.4(MYH6):c.2928+5G>A rs28730772
NM_002471.4(MYH6):c.2946G>A (p.Glu982=) rs145274612
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_002471.4(MYH6):c.3178G>A (p.Asp1060Asn)
NM_002471.4(MYH6):c.3303G>A (p.Val1101=) rs143825034
NM_002471.4(MYH6):c.3388G>A (p.Ala1130Thr) rs28730771
NM_002471.4(MYH6):c.3447C>G (p.Ser1149Arg) rs564367705
NM_002471.4(MYH6):c.3480C>T (p.Ser1160=) rs373345984
NM_002471.4(MYH6):c.3508G>A (p.Glu1170Lys) rs727503236
NM_002471.4(MYH6):c.3573C>T (p.Ala1191=) rs727505358
NM_002471.4(MYH6):c.3609C>G (p.Ala1203=) rs149369904
NM_002471.4(MYH6):c.3627C>T (p.Ile1209=) rs147871745
NM_002471.4(MYH6):c.3883G>C (p.Glu1295Gln) rs34935550
NM_002471.4(MYH6):c.3903G>A (p.Ser1301=) rs201804323
NM_002471.4(MYH6):c.3927T>C (p.Ser1309=) rs115742584
NM_002471.4(MYH6):c.3979-8_3979-7delinsGC rs727503235
NM_002471.4(MYH6):c.4136C>T (p.Thr1379Met) rs145611185
NM_002471.4(MYH6):c.4193G>A (p.Arg1398Gln) rs150815925
NM_002471.4(MYH6):c.4206C>T (p.Ala1402=) rs111638554
NM_002471.4(MYH6):c.4207G>A (p.Glu1403Lys) rs769398160
NM_002471.4(MYH6):c.4320T>A (p.Ala1440=) rs145566711
NM_002471.4(MYH6):c.4359+5A>G rs193283041
NM_002471.4(MYH6):c.4359+8A>C rs188675676
NM_002471.4(MYH6):c.4360-7C>T rs58949384
NM_002471.4(MYH6):c.4611G>A (p.Val1537=) rs142983918
NM_002471.4(MYH6):c.4683C>T (p.Leu1561=)
NM_002471.4(MYH6):c.4782G>A (p.Arg1594=) rs142823394
NM_002471.4(MYH6):c.4899C>T (p.His1633=) rs61742474
NM_002471.4(MYH6):c.4960-9G>A rs557113705
NM_002471.4(MYH6):c.4986G>A (p.Ala1662=) rs77416370
NM_002471.4(MYH6):c.5293G>A (p.Ala1765Thr) rs397516775
NM_002471.4(MYH6):c.5439G>A (p.Gln1813=) rs200854143
NM_002471.4(MYH6):c.5475G>A (p.Glu1825=) rs79143968
NM_002471.4(MYH6):c.5514G>T (p.Ser1838=) rs727503232
NM_002471.4(MYH6):c.643-5C>T rs199859986
NM_002471.4(MYH6):c.693C>T (p.Phe231=)
NM_002471.4(MYH6):c.831G>T (p.Gln277His) rs140660481
NM_002471.4(MYH6):c.909G>A (p.Leu303=) rs17091623

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.