MYL3 missense variants in ExAC

MYL3 gene summary
MYL3 variants in HCM, DCM

The table below lists the MYL3 missense variants found in the ExAC population database. Click on each variant for more details, including presence in the 1000 Genomes and Exome Sequencing Project databases, a breakdown by ethnic class and the variant's role in inherited cardiac disease. Use the form below to customise the variant selection. The table can be sorted by variant location, variant type or ExAC frequency.




No. Genomic coord.✝ Variant (CDS)▼ Variant (Protein) Variant Type▼ ExAC frequency▼Populations*
1. 46899901 c.532G>A p.D178N missense 0.00026373●●●●●●
2. 46902303 c.170C>A p.A57D missense 0.00011538●●●●●●
3. 46904789 c.92G>A p.R31H missense 0.00010709●●●●●●
4. 46902303 c.170C>G p.A57G missense 0.00009066●●●●●●
5. 46902253 c.220G>A p.G74R missense 0.00005769●●●●●●
6. 46899903 c.530A>G p.E177G missense 0.00004945●●●●●●
7. 46904877 c.4G>C p.A2P missense 0.00004159●●●●●●
8. 46902228 c.245C>T p.A82V missense 0.00003298●●●●●●
9. 46902238 c.235G>A p.V79I missense 0.00003297●●●●●●
10. 46902467 c.140C>T p.T47I missense 0.00002480●●●●●●
11. 46904826 c.55G>T p.A19S missense 0.00002473●●●●●●
12. 46902285 c.188G>A p.R63H missense 0.00002472●●●●●●
13. 46900985 c.461G>A p.R154H missense 0.00002471●●●●●●
14. 46900970 c.476C>T p.T159M missense 0.00002471●●●●●●
15. 46904880 c.1A>G p.Met1? missense 0.00001666●●●●●●
16. 46902455 c.152T>C p.I51T missense 0.00001652●●●●●●
17. 46904808 c.73C>T p.P25S missense 0.00001648●●●●●●
18. 46904790 c.91C>T p.R31C missense 0.00001648●●●●●●
19. 46904787 c.94C>T p.P32S missense 0.00001648●●●●●●
20. 46900980 c.466G>A p.V156M missense 0.00001647●●●●●●
21. 46901099 c.347C>T p.P116L missense 0.00001647●●●●●●
22. 46900986 c.460C>T p.R154C missense 0.00001647●●●●●●
23. 46904873 c.8C>A p.P3H missense 0.00000832●●●●●●
24. 46904864 c.17C>G p.P6R missense 0.00000828●●●●●●
25. 46902471 c.136T>C p.F46L missense 0.00000827●●●●●●
26. 46902172 c.301C>G p.Q101E missense 0.00000827●●●●●●
27. 46902179 c.294G>T p.K98N missense 0.00000827●●●●●●
28. 46902193 c.280C>T p.R94C missense 0.00000826●●●●●●
29. 46899945 c.488G>C p.R163T missense 0.00000826●●●●●●
30. 46899948 c.485A>G p.E162G missense 0.00000826●●●●●●
31. 46904851 c.30G>C p.K10N missense 0.00000826●●●●●●
32. 46902455 c.152T>G p.I51S missense 0.00000826●●●●●●
33. 46899949 c.484G>A p.E162K missense 0.00000826●●●●●●
34. 46899940 c.493A>G p.T165A missense 0.00000825●●●●●●
35. 46904845 c.36T>G p.D12E missense 0.00000825●●●●●●
36. 46902199 c.274G>A p.V92M missense 0.00000825●●●●●●
37. 46901129 c.317C>A p.T106N missense 0.00000824●●●●●●
38. 46901000 c.446T>C p.M149T missense 0.00000824●●●●●●
39. 46902232 c.241C>T p.R81W missense 0.00000824●●●●●●
40. 46901046 c.400G>T p.V134L missense 0.00000824●●●●●●
41. 46900985 c.461G>T p.R154L missense 0.00000824●●●●●●
42. 46901072 c.374A>G p.K125R missense 0.00000824●●●●●●
43. 46904790 c.91C>G p.R31G missense 0.00000824●●●●●●
44. 46904820 c.61C>T p.P21S missense 0.00000824●●●●●●
45. 46902313 c.160T>G p.F54V missense 0.00000824●●●●●●
46. 46902286 c.187C>T p.R63C missense 0.00000824●●●●●●
47. 46901135 c.311T>C p.L104P missense 0.00000824●●●●●●
48. 46900990 c.456G>T p.E152D missense 0.00000824●●●●●●
49. 46901057 c.389A>T p.Y130F missense 0.00000824●●●●●●
50. 46902246 c.227G>A p.C76Y missense 0.00000824●●●●●●
51. 46904796 c.85C>G p.P29A missense 0.00000824●●●●●●
52. 46902289 c.184G>A p.D62N missense 0.00000824●●●●●●
53. 46899876 c.557A>C p.E186A missense 0.00000824●●●●●●
54. 46904775 c.106G>A p.E36K missense 0.00000824●●●●●●
55. 46902271 c.202G>C p.E68Q missense 0.00000824●●●●●●
56. 46899912 c.521C>T p.A174V missense 0.00000824●●●●●●
57. 46902297 c.176T>C p.M59T missense 0.00000824●●●●●●
58. 46901007 c.439A>G p.T147A missense 0.00000824●●●●●●
59. 46904799 c.82G>A p.E28K missense 0.00000824●●●●●●
60. 46902279 c.194C>G p.P65R missense 0.00000824●●●●●●

* This highlights the relative frequency of the variant in the ExAC populations - Non-Finnish European, African, East Asian, South Asian, American and Finnish. Higher frequencies are denoted by darker shades of green, variants absent in a population are coloured light gray.

✝ Genomic coordinates refer to the GRCh37 release of the human genome.