MYO6 splice variants in ExAC


The table below lists the MYO6 splice 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 frequencyPopulations*
1. 76545684 c.553+11T>C splice site 0.12145742
2. 76570816 c.1546+4_1546+5delTG splice site 0.02465735
3. 76566810 c.1224-4A>G splice site 0.00201392
4. 76540124 c.262-9C>T splice site 0.00062053
5. 76570818 c.1546+6T>C splice site 0.00020759
6. 76551103 c.816+8A>G splice site 0.00019886
7. 76545683 c.553+10A>G splice site 0.00017442
8. 76538254 c.188-3T>C splice site 0.00011604
9. 76558256 c.1078+8_1078+12delTTTTA splice site 0.00010209
10. 76608087 c.3138-3T>C splice site 0.00004957
11. 0 c.-47-3C>G splice site 0.00004946
12. 76602418 c.3107+11C>T splice site 0.00004224
13. 76558254 c.1078+6C>T splice site 0.00004183
14. 76618209 c.3281-4A>G splice site 0.00004142
15. 76550405 c.651+6T>C splice site 0.00003677
16. 76542669 c.497+5G>A splice site 0.00002492
17. 76624005 c.3658+7A>G splice site 0.00002478
18. 76618352 c.3412+8G>T splice site 0.00002477
19. 76589845 c.2286+8T>C splice site 0.00002325
20. 76589841 c.2286+4A>T splice site 0.00002252
21. 76550924 c.652-7T>G splice site 0.00001688
22. 76550294 c.554-8C>T splice site 0.00001665
23. 76604983 c.3137+6T>G splice site 0.00001665
24. 76604982 c.3137+5G>A splice site 0.00001664
25. 76617431 c.3280+6_3280+9delTGTT splice site 0.00001661
26. 76540269 c.391+7G>C splice site 0.00001659
27. 76554609 c.817-5C>T splice site 0.00001654
28. 76554607 c.817-7G>C splice site 0.00001654
29. 76540125 c.262-8G>A splice site 0.00001654
30. 76576345 c.1770+7A>G splice site 0.00001652
31. 76576342 c.1770+4A>G splice site 0.00001651
32. 0 c.-47-3C>T splice site 0.00001649
33. 76572445 c.1674+5G>A splice site 0.00001648
34. 76564848 c.1079-8T>C splice site 0.00001549
35. 76600939 c.2868-6T>C splice site 0.00001525
36. 76600942 c.2868-3T>C splice site 0.00001413
37. 76564851 c.1079-5A>G splice site 0.00001398
38. 76601030 c.2946+7A>G splice site 0.00001164
39. 76568714 c.1473+4A>G splice site 0.00001142
40. 76589842 c.2286+5A>G splice site 0.00001132
41. 76595714 c.2417-7C>T splice site 0.00001034
42. 76580358 c.1945-6T>G splice site 0.00000890
43. 76572305 c.1547-8T>G splice site 0.00000881
44. 76572306 c.1547-7G>A splice site 0.00000878
45. 76580406 c.1983+4A>G splice site 0.00000857
46. 76542554 c.392-5C>T splice site 0.00000834
47. 76604942 c.3108-6T>C splice site 0.00000834
48. 76558252 c.1078+4T>G splice site 0.00000833
49. 76550295 c.554-7T>A splice site 0.00000832
50. 76542669 c.497+5G>C splice site 0.00000831
51. 76542671 c.497+7A>G splice site 0.00000831
52. 76540268 c.391+6T>A splice site 0.00000830
53. 76540268 c.391+6T>C splice site 0.00000830
54. 76617319 c.3177-3C>T splice site 0.00000830
55. 76545679 c.553+6G>A splice site 0.00000830
56. 76618206 c.3281-7T>C splice site 0.00000829
57. 76618205 c.3281-8A>C splice site 0.00000829
58. 76623777 c.3440-3T>C splice site 0.00000829
59. 76554699 c.897+5A>G splice site 0.00000829
60. 76623775 c.3440-5A>G splice site 0.00000829
61. 76608136 c.3176+8C>G splice site 0.00000827
62. 76596719 c.2658+8A>G splice site 0.00000827
63. 76608086 c.3138-4G>C splice site 0.00000826
64. 76558070 c.900C>T splice site 0.00000825
65. 76624524 c.3659-6A>G splice site 0.00000825
66. 76558062 c.898-6T>C splice site 0.00000825
67. 76591545 c.2416+10T>C splice site 0.00000824
68. 76589529 c.2078-8G>C splice site 0.00000824
69. 76589532 c.2078-5T>A splice site 0.00000824
70. 76566975 c.1381+4A>C splice site 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.