SCN10A splice variants in ExAC


The table below lists the SCN10A 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. 38784029 c.1868-9A>G splice site 0.65368451
2. 38743331 c.4656G>A p.A1552A splice site 0.00136060
3. 38797453 c.1291-4G>A splice site 0.00027209
4. 38797454 c.1291-5C>T splice site 0.00022266
5. 38760135 c.3681+9C>T splice site 0.00018194
6. 38830536 c.390-9G>A splice site 0.00014264
7. 38791556 c.1867+8C>T splice site 0.00014222
8. 38755443 c.3804+6delT splice site 0.00010780
9. 38783774 c.2106+8C>T splice site 0.00006671
10. 38743325 c.4657+5G>A splice site 0.00005224
11. 38798369 c.1093-7C>A splice site 0.00004959
12. 38802878 c.692-4G>A splice site 0.00004288
13. 38763902 c.3354A>G splice site 0.00004157
14. 38791559 c.1867+5G>A splice site 0.00003339
15. 38830442 c.470+5G>A splice site 0.00003338
16. 38750962 c.4281+7G>T splice site 0.00002600
17. 38802881 c.692-7C>T splice site 0.00002582
18. 38802879 c.692-5C>T splice site 0.00002574
19. 38798365 c.1093-3C>A splice site 0.00002479
20. 38748883 c.4282-9T>C splice site 0.00002475
21. 38765048 c.3229-4G>A splice site 0.00002188
22. 38765042 c.3231A>G splice site 0.00001978
23. 38793710 c.1755G>A splice site 0.00001807
24. 38750964 c.4281+5G>A splice site 0.00001728
25. 38770403 c.2281-11T>C splice site 0.00001726
26. 38740051 c.4660C>T splice site 0.00001676
27. 38791557 c.1867+7G>A splice site 0.00001672
28. 38812763 c.599+7A>T splice site 0.00001664
29. 38791683 c.1756-8C>T splice site 0.00000946
30. 38791680 c.1756-5A>T splice site 0.00000924
31. 38752394 c.4090-6C>T splice site 0.00000922
32. 38752386 c.4092A>C p.A1364A splice site 0.00000908
33. 38793705 c.1755+5G>C splice site 0.00000904
34. 38793705 c.1755+5G>A splice site 0.00000904
35. 38768090 c.3087+7G>A splice site 0.00000904
36. 38770025 c.2640+8G>A splice site 0.00000900
37. 38770028 c.2640+5G>C splice site 0.00000899
38. 38798657 c.951-7G>C splice site 0.00000883
39. 38802679 c.883+4A>G splice site 0.00000877
40. 38751113 c.4144-7G>C splice site 0.00000868
41. 38751111 c.4144-5C>T splice site 0.00000866
42. 38751112 c.4144-6T>G splice site 0.00000866
43. 38750963 c.4281+6T>C splice site 0.00000865
44. 38750963 c.4281+6T>G splice site 0.00000865
45. 38770399 c.2281-7T>C splice site 0.00000860
46. 38802878 c.692-4G>T splice site 0.00000858
47. 38770395 c.2281-3C>T splice site 0.00000856
48. 38766659 c.3228+6T>A splice site 0.00000851
49. 38802873 c.693C>T splice site 0.00000850
50. 38802872 c.694C>T p.L232L splice site 0.00000849
51. 38768551 c.2641-8C>A splice site 0.00000848
52. 38740061 c.4658-8T>C splice site 0.00000846
53. 38768548 c.2641-5T>C splice site 0.00000842
54. 38781185 c.2107-6T>C splice site 0.00000838
55. 38830527 c.390G>A p.S130S splice site 0.00000837
56. 38791558 c.1867+6T>G splice site 0.00000835
57. 38753942 c.3805-6C>T splice site 0.00000835
58. 38830441 c.470+6T>C splice site 0.00000835
59. 38753943 c.3805-7C>A splice site 0.00000835
60. 38763910 c.3353-7C>A splice site 0.00000834
61. 38763908 c.3353-5C>A splice site 0.00000833
62. 38812762 c.599+8T>C splice site 0.00000833
63. 38753649 c.4089+3G>A splice site 0.00000831
64. 38755444 c.3804+5G>C splice site 0.00000829
65. 38835225 c.270+7G>A splice site 0.00000827
66. 38798160 c.1290+5G>T splice site 0.00000827
67. 38760136 c.3681+8G>A splice site 0.00000827
68. 38798159 c.1290+6dupT splice site 0.00000827
69. 38760138 c.3681+6T>C splice site 0.00000826
70. 38748877 c.4282-3C>T splice site 0.00000825
71. 38797453 c.1291-4G>C splice site 0.00000825
72. 38797271 c.1461+8G>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.