DSP splice variants in ExAC


The table below lists the DSP 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. 7556058 c.273+5G>A splice site 0.00035156
2. 7568145 c.1266+6G>T splice site 0.00059123
3. 7571824 c.1903+7T>C splice site 0.00703713
4. 7576527 c.2631G>A p.R877R splice site 0.77179183
5. 7556063 c.273+10C>T splice site 0.02513941
6. 7563020 c.726+7G>C splice site 0.00010710
7. 7563971 c.729C>T p.R243R splice site 0.00014005
8. 7578691 c.2986-6T>A splice site 0.00035525
9. 7567579 c.1045-8T>C splice site 0.00000824
10. 7569580 c.1574+7C>T splice site 0.00004118
11. 7577194 c.2796C>T p.N932N splice site 0.00005854
12. 7577187 c.2794-5_2794-4insA splice site 0.00010119
13. 7556060 c.273+7T>C splice site 0.00000907
14. 7567688 c.1140+6T>C splice site 0.00009071
15. 7558345 c.274-4T>G splice site 0.00003295
16. 7558504 c.422+7delT splice site 0.00000942
17. 7558503 c.422+6G>T splice site 0.00000942
18. 7559453 c.423-6T>G splice site 0.00000828
19. 7562880 c.598-5C>T splice site 0.00003295
20. 7562881 c.598-4G>A splice site 0.00001647
21. 7562887 c.600G>C splice site 0.00000824
22. 7563017 c.726+4C>T splice site 0.00000824
23. 7563017 c.726+4C>G splice site 0.00000824
24. 7563962 c.727-7C>G splice site 0.00000824
25. 7564024 c.777+5G>A splice site 0.00000824
26. 7565753 c.939C>T splice site 0.00014011
27. 7565758 c.939+5G>T splice site 0.00000824
28. 7566717 c.1044+3A>G splice site 0.00000835
29. 7567584 c.1045-3C>T splice site 0.00002471
30. 7567688 c.1140+6T>A splice site 0.00000825
31. 7568145 c.1266+6G>A splice site 0.00006662
32. 7568829 c.1419+7A>T splice site 0.00000825
33. 7569571 c.1572C>T splice site 0.00000824
34. 7569581 c.1574+8A>G splice site 0.00000824
35. 7570666 c.1575-4T>G splice site 0.00000824
36. 7570800 c.1701+4T>C splice site 0.00001648
37. 7571820 c.1903+3C>T splice site 0.00000826
38. 7571821 c.1903+4G>A splice site 0.00004958
39. 7574312 c.2131-7T>C splice site 0.00000825
40. 7574314 c.2131-5G>C splice site 0.00006602
41. 7575520 c.2437-8T>C splice site 0.00000828
42. 7576522 c.2631-5C>T splice site 0.00003314
43. 7576696 c.2793+7G>A splice site 0.00000826
44. 7577186 c.2794-6G>A splice site 0.00001690
45. 7578008 c.2878-4G>A splice site 0.00003296
46. 7578119 c.2985G>A splice site 0.00001648
47. 7578127 c.2985+8T>C splice site 0.00000825
48. 7579505 c.3085-3C>T splice site 0.00000872
49. 7581810 c.5379+8C>A splice site 0.00002562
50. 7582871 c.5380-4C>G splice site 0.00000827

* 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.