ACTN1 splice variants in ExAC


The table below lists the ACTN1 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. 69392264 c.220+11A>C splice site 0.71034431
2. 69378863 c.427+10T>C splice site 0.20600989
3. 69371366 c.676+6A>G splice site 0.00198756
4. 69346834 c.2134-9G>A splice site 0.00098549
5. 69371363 c.676+9C>T splice site 0.00082489
6. 69346835 c.2134-10C>T splice site 0.00043895
7. 69345797 c.2281-11C>T splice site 0.00028955
8. 69369188 c.762+6C>T splice site 0.00011537
9. 69356857 c.1233C>T p.D411D splice site 0.00009237
10. 69345699 c.2361+7G>A splice site 0.00007425
11. 69376120 c.516-7C>T splice site 0.00006686
12. 69345170 c.2427+5C>T splice site 0.00005636
13. 69392268 c.220+7C>T splice site 0.00004989
14. 69387717 c.340+6G>T splice site 0.00003304
15. 69345245 c.2362-5C>T splice site 0.00002742
16. 69360462 c.765G>A p.A255A splice site 0.00002480
17. 69345699 c.2361+7G>T splice site 0.00002475
18. 69345245 c.2362-5C>G splice site 0.00001828
19. 69345250 c.2362-10C>T splice site 0.00001823
20. 69349168 c.1953+7C>A splice site 0.00001676
21. 69351029 c.1495-4C>T splice site 0.00001662
22. 69347713 c.1954-7T>G splice site 0.00001656
23. 69360368 c.855+4G>T splice site 0.00001652
24. 69376031 c.594+4delT splice site 0.00001652
25. 69369283 c.677-4A>G splice site 0.00001648
26. 69356851 c.1234+5G>C splice site 0.00001070
27. 69345169 c.2427+6G>A splice site 0.00000941
28. 69345247 c.2362-7C>T splice site 0.00000910
29. 69341742 c.2587-8C>T splice site 0.00000889
30. 69341737 c.2587-3C>T splice site 0.00000879
31. 69343796 c.2586+3G>T splice site 0.00000851
32. 69392397 c.106-8C>T splice site 0.00000843
33. 69392387 c.108A>T splice site 0.00000837
34. 69376119 c.516-6G>A splice site 0.00000835
35. 69358762 c.1086+8C>T splice site 0.00000833
36. 69351028 c.1495-3C>T splice site 0.00000831
37. 69349317 c.1819-8T>C splice site 0.00000830
38. 69358770 c.1086G>A splice site 0.00000830
39. 69349314 c.1819-5C>T splice site 0.00000829
40. 69360467 c.763-3C>T splice site 0.00000828
41. 69360364 c.855+8C>A splice site 0.00000827
42. 69376770 c.428-11C>T splice site 0.00000827
43. 69343963 c.2428-6C>T splice site 0.00000827
44. 69376763 c.428-4A>T splice site 0.00000826
45. 69371365 c.676+7G>A splice site 0.00000825
46. 69345700 c.2361+6C>T splice site 0.00000825
47. 69345701 c.2361+5T>G splice site 0.00000825
48. 69378869 c.427+4G>A splice site 0.00000824
49. 69369187 c.762+7G>C 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.