MYOM1 splice variants in ExAC


The table below lists the MYOM1 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. 3214924 c.290+8G>A splice site 0.00010294
2. 3214924 c.290+8G>T splice site 0.00000936
3. 3193811 c.431+5G>C splice site 0.00002503
4. 3189095 c.432-10_432-8delTGT splice site 0.00040116
5. 3188740 c.771+6A>G splice site 0.00006509
6. 3187640 c.772-5T>C splice site 0.00006808
7. 3187639 c.772-4T>C splice site 0.00000963
8. 3187480 c.927G>C splice site 0.00000829
9. 3187475 c.929+3A>G splice site 0.00001658
10. 3174214 c.1023-8T>C splice site 0.00000831
11. 3174110 c.1111+8delT splice site 0.00000828
12. 3174009 c.1112-11T>C splice site 0.00364673
13. 3174002 c.1112-4C>T splice site 0.00003315
14. 3174001 c.1112-3T>C splice site 0.00000829
15. 3168816 c.1338C>T p.N446N splice site 0.26201991
16. 3168804 c.1339+11A>C splice site 0.00000834
17. 3164441 c.1340-4C>A splice site 0.00034944
18. 3155085 c.1503T>C splice site 0.00001976
19. 3151902 c.1644-11C>T splice site 0.00013414
20. 3151896 c.1644-5T>A splice site 0.00001667
21. 3151895 c.1644-4T>G splice site 0.00001666
22. 3151685 c.1843+7A>C splice site 0.00000859
23. 3151682 c.1843+10T>G splice site 0.00104287
24. 3149140 c.1900+3A>C splice site 0.00386241
25. 3149137 c.1900+6_1900+8delAAG splice site 0.00027355
26. 3149136 c.1900+7delA splice site 0.00000829
27. 3149136 c.1900+7A>G splice site 0.00000829
28. 3142070 c.1901-9_1901-7delGTT splice site 0.00001673
29. 3142060 c.1902G>A splice site 0.00024236
30. 3135733 c.2026-5T>C splice site 0.00000838
31. 3135732 c.2026-4G>A splice site 0.00000838
32. 3134826 c.2210-4T>G splice site 0.01005893
33. 3134644 c.2384+4A>T splice site 0.00085628
34. 3131500 c.2385-6T>G splice site 0.00000900
35. 3131369 c.2506+4A>G splice site 0.00000830
36. 3131368 c.2506+5G>A splice site 0.00000830
37. 3129521 c.2507-4G>A splice site 0.00000861
38. 3129520 c.2507-3T>C splice site 0.00000860
39. 3126691 c.2991+8C>A splice site 0.00079536
40. 3126691 c.2991+8C>T splice site 0.00002743
41. 3119999 c.2992-6T>C splice site 0.00001718
42. 3119859 c.3118+8A>G splice site 0.00000849
43. 3116512 c.3120A>G splice site 0.00001800
44. 3116325 c.3303+4delA splice site 0.00008640
45. 3112290 c.3418+6C>A splice site 0.00001686
46. 3102635 c.3419-7C>A splice site 0.00000835
47. 3102632 c.3419-4G>T splice site 0.00000834
48. 3100432 c.3576-8T>A splice site 0.00001053
49. 3100430 c.3576-6C>G splice site 0.00001041
50. 3100429 c.3576-5C>T splice site 0.44223876
51. 3100428 c.3576-4G>A splice site 0.00000897
52. 3100428 c.3576-4G>C splice site 0.00000897
53. 3100314 c.3682+4A>G splice site 0.00000837
54. 3100212 c.3683-11T>C splice site 0.00000828
55. 3100208 c.3683-7C>T splice site 0.00001656
56. 3100207 c.3683-6C>T splice site 0.00000828
57. 3100158 c.3726A>C p.P1242P splice site 0.00000828
58. 3100155 c.3727+2dupT splice site 0.00000828
59. 3094312 c.3728-8T>G splice site 0.00001046
60. 3094168 c.3864G>A splice site 0.00000830
61. 3094165 c.3864+3A>C splice site 0.00000830
62. 3090808 c.3865-8C>T splice site 0.00000830
63. 3090807 c.3865-7A>C splice site 0.00011612
64. 3090805 c.3865-5delT splice site 0.00000829
65. 3090803 c.3865-3A>G splice site 0.00000829
66. 3090798 c.3867A>G splice site 0.00000829
67. 3089598 c.4010-4G>T splice site 0.00000938
68. 3089531 c.4069+4A>C splice site 0.00247269
69. 3089167 c.4137+5G>C splice site 0.00002549
70. 3086156 c.4138-7C>G splice site 0.00000874
71. 3086033 c.4251+3A>G splice site 0.00000848
72. 3086030 c.4251+6C>T splice site 0.00003427
73. 3086029 c.4251+7G>A splice site 0.00004318
74. 3086029 c.4251+7G>T splice site 0.00000864
75. 3086027 c.4251+9T>C splice site 0.00004349
76. 3085135 c.4252-5delC splice site 0.00001486
77. 3084033 c.4340-8C>G splice site 0.00011267
78. 3084030 c.4340-5C>T splice site 0.00002719
79. 3083980 c.4378+7C>G splice site 0.00002437
80. 3083896 c.4379-4T>G splice site 0.00034286
81. 3083891 c.4380T>G splice site 0.00002856
82. 3083784 c.4484+3A>C splice site 0.00004266
83. 3079345 c.4485-5C>T splice site 0.00010360
84. 3079343 c.4485-3C>T splice site 0.00001714
85. 3079178 c.4647A>G p.Q1549Q splice site 0.00001747
86. 3079170 c.4648+7A>G splice site 0.00018218
87. 3079169 c.4648+8_4648+9delGA splice site 0.00000924
88. 3079169 c.4648+8G>T splice site 0.00000916
89. 3075765 c.4649-6T>C splice site 0.00027906
90. 3075758 c.4650A>G splice site 0.00001893
91. 3075720 c.4685+3_4685+6delAAGT splice site 0.00014154
92. 3075712 c.4685+11G>T splice site 0.53986869
93. 3075445 c.4708+7A>C splice site 0.00000830
94. 3071822 c.4764+10A>G splice site 0.00065943
95. 3067557 c.4765-4G>T splice site 0.00000842
96. 3067556 c.4765-3C>T splice site 0.00000841

* 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.