VCL splice variants in ExAC


The table below lists the VCL 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. 75758140 c.168+7G>T splice site 0.00008134
2. 75802834 c.169-7C>G splice site 0.00004150
3. 75802837 c.169-4G>A splice site 0.00000829
4. 75802917 c.239+6T>G splice site 0.00002476
5. 75802920 c.239+9T>C splice site 0.00002477
6. 75830422 c.240-6_240-5insT splice site 0.00004943
7. 75830424 c.240-4A>G splice site 0.00002471
8. 75830840 c.498A>G splice site 0.00002479
9. 75832609 c.621A>T splice site 0.00000824
10. 75832614 c.622+4C>T splice site 0.00058493
11. 75832614 c.622+4C>A splice site 0.00001648
12. 75832614 c.622+4C>G splice site 0.00004119
13. 75834665 c.783+4C>T splice site 0.00000826
14. 75834666 c.783+5G>A splice site 0.00000826
15. 75842309 c.874+7C>G splice site 0.00000830
16. 75842310 c.874+8T>C splice site 0.00000830
17. 75843274 c.1022+3A>T splice site 0.00001686
18. 75849112 c.1176+5T>C splice site 0.00000826
19. 75849774 c.1177-7T>C splice site 0.00000824
20. 75849775 c.1177-6G>C splice site 0.00002473
21. 75849776 c.1177-5T>C splice site 0.00006593
22. 75849961 c.1352+5G>A splice site 0.00006592
23. 75854218 c.1542C>T p.V514V splice site 0.00121003
24. 75854223 c.1543+4A>G splice site 0.00000989
25. 75855410 c.1544-4C>T splice site 0.00000824
26. 75855617 c.1743+4G>A splice site 0.00002494
27. 75855619 c.1743+6A>T splice site 0.00014976
28. 75855619 c.1743+6A>G splice site 0.00006656
29. 75857097 c.1872+7A>G splice site 0.00000827
30. 75860698 c.1873-8T>G splice site 0.00000831
31. 75860702 c.1873-4C>T splice site 0.00000830
32. 75860855 c.2022G>A splice site 0.00000937
33. 75863580 c.2025G>A p.V675V splice site 0.00253711
34. 75866982 c.2435-6G>A splice site 0.00000824
35. 75868729 c.2560C>T splice site 0.00013205
36. 75868922 c.2745+8G>A splice site 0.00000829
37. 75871659 c.2746-8C>T splice site 0.00004167
38. 75871660 c.2746-7G>A splice site 0.00001665
39. 75871662 c.2746-5C>T splice site 0.00000831
40. 75871669 c.2748G>A splice site 0.00000829
41. 75871874 c.2949+4C>T splice site 0.00000824
42. 75873936 c.2950-6C>T splice site 0.00000828
43. 75874151 c.3153+6C>T splice site 0.00001669
44. 75874152 c.3153+7G>A splice site 0.00000838
45. 75874547 c.3154-6C>T splice site 0.00001944
46. 75874547 c.3154-6C>G splice site 0.00001944
47. 75874548 c.3154-5T>G splice site 0.00001895
48. 75874550 c.3154-3T>C splice site 0.00001787
49. 75874662 c.3258+5G>A splice site 0.00002288
50. 75874667 c.3258+10A>T splice site 0.00371424
51. 75877770 c.3259-11T>C splice site 0.00000824
52. 75877774 c.3259-7C>T splice site 0.00000824
53. 75877778 c.3259-3C>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.