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