NEBL splice variants in ExAC


The table below lists the NEBL 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. 21141469 c.1008+5A>G splice site 0.97092899
2. 21120116 c.1671+9T>C splice site 0.38930519
3. 21177144 c.259-8dupT splice site 0.02581898
4. 21104651 c.2149-5G>A splice site 0.00756280
5. 21177144 c.259-8delT splice site 0.00416788
6. 21169720 c.480+3A>G splice site 0.00324702
7. 21178889 c.154-11C>A splice site 0.00286361
8. 21134303 c.1117-6T>G splice site 0.00190368
9. 21141470 c.1008+4C>T splice site 0.00143633
10. 21120521 c.1450-9T>G splice site 0.00138572
11. 21102862 c.2346+6G>A splice site 0.00048031
12. 21185962 c.82-4A>G splice site 0.00023067
13. 21177021 c.369+5G>A splice site 0.00019840
14. 21106525 c.2148+4T>C splice site 0.00019793
15. 21112130 c.1962+7A>G splice site 0.00018146
16. 21158660 c.582+9T>C splice site 0.00015703
17. 21115368 c.1869+8C>G splice site 0.00015678
18. 21129785 c.1228-7C>T splice site 0.00015375
19. 21108353 c.2055G>A splice site 0.00013180
20. 21134182 c.1227+5G>A splice site 0.00011759
21. 21148635 c.798+7T>A splice site 0.00010865
22. 21141466 c.1008+8C>G splice site 0.00007443
23. 21134183 c.1227+4C>T splice site 0.00005861
24. 21102863 c.2346+5G>A splice site 0.00005795
25. 21147169 c.903C>T p.G301G splice site 0.00004969
26. 21108345 c.2055+8G>A splice site 0.00004943
27. 21097594 c.2612-6A>G splice site 0.00004167
28. 21139437 c.1009-6A>G splice site 0.00002508
29. 21097594 c.2612-6A>C splice site 0.00002500
30. 21177022 c.369+4G>A splice site 0.00002480
31. 21104554 c.2241G>A p.S747S splice site 0.00002478
32. 21108346 c.2055+7C>T splice site 0.00002471
33. 21076236 c.2763A>G splice site 0.00001885
34. 21134300 c.1117-3C>T splice site 0.00001683
35. 21134182 c.1227+5G>C splice site 0.00001680
36. 21178881 c.154-3dupT splice site 0.00001670
37. 21148636 c.798+6T>C splice site 0.00001670
38. 21147164 c.903+5G>A splice site 0.00001659
39. 21098729 c.2611+6A>G splice site 0.00001657
40. 21169842 c.370-9G>A splice site 0.00001655
41. 21177020 c.369+6G>A splice site 0.00001654
42. 21169713 c.480+10C>A splice site 0.00001648
43. 21108345 c.2055+8G>C splice site 0.00001648
44. 21148763 c.685-8T>C splice site 0.00001094
45. 21076131 c.2868A>G splice site 0.00001040
46. 21177144 c.259-8T>C splice site 0.00000976
47. 21141584 c.904-6T>C splice site 0.00000976
48. 21141583 c.904-5T>G splice site 0.00000971
49. 21129662 c.1338+6T>C splice site 0.00000883
50. 21117451 c.1776+8G>A splice site 0.00000864
51. 21117459 c.1776G>A p.A592A splice site 0.00000857
52. 21177140 c.259-4C>G splice site 0.00000850
53. 21147277 c.799-4A>G splice site 0.00000844
54. 21120516 c.1450-4G>A splice site 0.00000844
55. 21112227 c.1872G>A splice site 0.00000842
56. 21101867 c.2349A>G splice site 0.00000840
57. 21115466 c.1779A>G splice site 0.00000835
58. 21178876 c.156C>A splice site 0.00000833
59. 21178876 c.156C>T splice site 0.00000833
60. 21148642 c.798T>C splice site 0.00000832
61. 21102981 c.2242-9A>G splice site 0.00000831
62. 21186051 c.81+3G>A splice site 0.00000831
63. 21186046 c.81+8A>G splice site 0.00000828
64. 21120120 c.1671+5G>C splice site 0.00000828
65. 21158661 c.582+8C>G splice site 0.00000826
66. 21120395 c.1560+7C>G splice site 0.00000826
67. 21101699 c.2517T>G splice site 0.00000825
68. 21106529 c.2148T>C splice site 0.00000825
69. 21141469 c.1008+5A>T splice site 0.00000825
70. 21101692 c.2518+6C>G splice site 0.00000825
71. 21101695 c.2518+3A>T splice site 0.00000825
72. 21124434 c.1449+8G>C splice site 0.00000824
73. 21108452 c.1963-7C>G splice site 0.00000824
74. 21185882 c.153+5G>A splice site 0.00000824
75. 21157593 c.684A>G splice site 0.00000824
76. 21108443 c.1965C>G 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.