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

* 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.