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

* 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.