AKAP9 splice variants in ExAC


The table below lists the AKAP9 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. 91707197 c.6945+8C>T splice site 0.40764656
2. 91694541 c.5978-4A>G splice site 0.00260005
3. 91734981 c.11331-11A>T splice site 0.00174288
4. 91718853 c.9358+10A>G splice site 0.00104184
5. 91699336 c.6331-8T>C splice site 0.00062832
6. 91660820 c.4246-6A>T splice site 0.00035567
7. 91732147 c.11330+7A>G splice site 0.00025228
8. 91712477 c.8161-7G>A splice site 0.00021746
9. 91725996 c.9730-7G>A splice site 0.00021239
10. 91670215 c.4917+3A>C splice site 0.00012160
11. 91682037 c.5369-3T>C splice site 0.00011068
12. 91712478 c.8161-6T>A splice site 0.00009198
13. 91695863 c.6330+3A>G splice site 0.00009130
14. 91718693 c.9214-6T>C splice site 0.00008258
15. 91714125 c.8711-8T>C splice site 0.00005816
16. 91700331 c.6612+8G>T splice site 0.00004962
17. 91691579 c.5765-9G>A splice site 0.00004171
18. 91674531 c.5368+4C>T splice site 0.00003303
19. 91728998 c.10714-3C>T splice site 0.00003295
20. 91691581 c.5765-7A>G splice site 0.00002500
21. 91674311 c.5163-11T>C splice site 0.00002481
22. 91621530 c.405+5A>G splice site 0.00002477
23. 91709471 c.8019+5G>C splice site 0.00002197
24. 91727532 c.10713+4A>G splice site 0.00002005
25. 91708386 c.6946-7delT splice site 0.00001876
26. 91603022 c.49-3T>C splice site 0.00001865
27. 91722634 c.9578+4T>C splice site 0.00001737
28. 91724330 c.9579-7G>A splice site 0.00001688
29. 91724331 c.9579-6A>T splice site 0.00001686
30. 91707002 c.6766-8G>A splice site 0.00001654
31. 91570466 c.48+5G>A splice site 0.00001653
32. 91714260 c.8832+6A>C splice site 0.00001652
33. 91622377 c.576+8T>C splice site 0.00001652
34. 91622373 c.576+4T>G splice site 0.00001651
35. 91651548 c.3838-4A>G splice site 0.00001650
36. 91736599 c.11417-8T>A splice site 0.00001648
37. 91706163 c.6613-6T>C splice site 0.00001576
38. 91739428 c.11687-8T>C splice site 0.00001303
39. 91739429 c.11687-7C>T splice site 0.00001299
40. 91694535 c.5978-10_5978-8delTAA splice site 0.00001286
41. 91652121 c.3953-7A>G splice site 0.00001156
42. 91694785 c.6210+8T>C splice site 0.00001132
43. 91652125 c.3953-3T>C splice site 0.00001119
44. 91694542 c.5978-3C>T splice site 0.00001112
45. 91694777 c.6210T>C p.D2070D splice site 0.00001049
46. 91643642 c.3612G>A splice site 0.00001001
47. 91722638 c.9578+8A>G splice site 0.00000883
48. 91706326 c.6765+5_6765+8delTTAG splice site 0.00000881
49. 91682277 c.5601+5_5601+7delCCT splice site 0.00000873
50. 91722633 c.9578+3G>C splice site 0.00000866
51. 91722405 c.9359-6G>A splice site 0.00000865
52. 91712976 c.8646+7G>T splice site 0.00000857
53. 91691807 c.5977+7A>G splice site 0.00000857
54. 91691808 c.5977+8T>C splice site 0.00000857
55. 91712975 c.8646+6T>C splice site 0.00000856
56. 91727423 c.10608A>G splice site 0.00000853
57. 91622191 c.406-8T>G splice site 0.00000850
58. 91725996 c.9730-7G>C splice site 0.00000850
59. 91609652 c.351+5G>A splice site 0.00000850
60. 91725998 c.9730-5A>T splice site 0.00000847
61. 91624909 c.733-8_733-7insT splice site 0.00000844
62. 91691799 c.5976A>G splice site 0.00000843
63. 91700211 c.6508-8A>G splice site 0.00000843
64. 91671975 c.5059-7_5059-6insA splice site 0.00000833
65. 91671975 c.5059-7T>C splice site 0.00000833
66. 91711984 c.8160+8A>G splice site 0.00000832
67. 91711980 c.8160+4A>G splice site 0.00000831
68. 91724495 c.9729+8T>C splice site 0.00000831
69. 91726896 c.10399-4C>T splice site 0.00000830
70. 91714016 c.8709T>C splice site 0.00000829
71. 91724492 c.9729+5delT splice site 0.00000829
72. 91674316 c.5163-6A>T splice site 0.00000827
73. 91660822 c.4246-4G>A splice site 0.00000827
74. 91674315 c.5163-7T>G splice site 0.00000827
75. 91736744 c.11546+8T>C splice site 0.00000826
76. 91621530 c.405+5A>T splice site 0.00000826
77. 91718692 c.9214-7G>A splice site 0.00000826
78. 91660921 c.4338+3A>G splice site 0.00000826
79. 91714262 c.8832+8A>G splice site 0.00000826
80. 91714806 c.8833-3C>T splice site 0.00000826
81. 91660924 c.4338+6C>G splice site 0.00000826
82. 91570465 c.48+4G>A splice site 0.00000826
83. 91715539 c.9025-3T>G splice site 0.00000825
84. 91699520 c.6507G>A splice site 0.00000824
85. 91659205 c.4149-4T>C splice site 0.00000824
86. 91699523 c.6507+3G>A splice site 0.00000824
87. 91699526 c.6507+6G>T 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.