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