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