MYBPC3 splice variants in ExAC


The table below lists the MYBPC3 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. 47374165 c.25+9A>G splice site 0.00001663
2. 47373055 c.27C>A splice site 0.00001265
3. 47372054 c.405A>G splice site 0.00008359
4. 47372048 c.406+5G>C splice site 0.00004342
5. 47371668 c.407-5C>T splice site 0.00009541
6. 47371566 c.504G>A splice site 0.00004213
7. 47371321 c.654+4G>A splice site 0.00000924
8. 47371317 c.654+8C>A splice site 0.00000929
9. 47371315 c.654+10C>T splice site 0.00000931
10. 47371314 c.654+11C>T splice site 0.00022461
11. 47369966 c.772+9G>T splice site 0.00001483
12. 47369397 c.821+11A>T splice site 0.00004415
13. 47369236 c.822-5C>T splice site 0.00003631
14. 47369234 c.822-3C>T splice site 0.00003619
15. 47369231 c.822G>A splice site 0.00003579
16. 47369040 c.852-10C>G splice site 0.00004034
17. 47368591 c.906-11_906-9delCTG splice site 0.00010750
18. 47368588 c.906-8T>C splice site 0.00001792
19. 47368587 c.906-7G>T splice site 0.00027619
20. 47368195 c.909C>T p.D303D splice site 0.00061428
21. 47368180 c.924G>A splice site 0.00001842
22. 47368174 c.926+4A>G splice site 0.00000919
23. 47368170 c.926+8C>T splice site 0.00034935
24. 47367924 c.927-3C>T splice site 0.00002139
25. 47367750 c.1090+8C>T splice site 0.00000839
26. 47365183 c.1091-8G>A splice site 0.00001971
27. 47364818 c.1224-5T>C splice site 0.00001040
28. 47364805 c.1226+6T>C splice site 0.00006195
29. 47364709 c.1227-13G>A splice site 0.00000998
30. 47364701 c.1227-5C>A splice site 0.00001970
31. 47364700 c.1227-4C>G splice site 0.00000985
32. 47364568 c.1351+4G>A splice site 0.00000880
33. 47364491 c.1352-5G>C splice site 0.00001798
34. 47364491 c.1352-5G>A splice site 0.00000899
35. 47364302 c.1458-7C>T splice site 0.00001667
36. 47364300 c.1458-5G>A splice site 0.00003328
37. 47364299 c.1458-4C>T splice site 0.00000832
38. 47364130 c.1623G>A splice site 0.00001221
39. 47364125 c.1624+4A>T splice site 0.00001347
40. 47363715 c.1625-8C>G splice site 0.00002574
41. 47363714 c.1625-7C>A splice site 0.00000856
42. 47363535 c.1790+7G>A splice site 0.00602362
43. 47362795 c.1791G>C splice site 0.00002522
44. 47362546 c.1927+8T>C splice site 0.00002892
45. 47361347 c.1928-6C>T splice site 0.00000831
46. 47361197 c.2067+5T>G splice site 0.00002193
47. 47360959 c.2068-4C>G splice site 0.00000829
48. 47360869 c.2148+6_2148+9delTGAG splice site 0.00002484
49. 47360238 c.2149-8C>G splice site 0.00005510
50. 47360238 c.2149-8C>T splice site 0.00002204
51. 47360235 c.2149-5C>T splice site 0.00127947
52. 47360235 c.2149-5C>G splice site 0.00004337
53. 47360233 c.2149-3C>T splice site 0.00001091
54. 47360072 c.2307C>T splice site 0.00002489
55. 47360068 c.2308+3G>A splice site 0.00000830
56. 47360063 c.2308+8C>T splice site 0.00004153
57. 47359235 c.2413+6T>C splice site 0.00002112
58. 47359234 c.2413+7G>A splice site 0.00002084
59. 47358943 c.2601C>T p.I867I splice site 0.00462683
60. 47357570 c.2603-8C>T splice site 0.00001495
61. 47357567 c.2603-5C>A splice site 0.00001500
62. 47357416 c.2737+12C>T splice site 0.10085737
63. 47356766 c.2738-6C>A splice site 0.00000867
64. 47356764 c.2738-4C>A splice site 0.00000867
65. 47356594 c.2904G>C splice site 0.00001089
66. 47355308 c.2995-5C>G splice site 0.00006070
67. 47355301 c.2997C>T p.G999G splice site 0.00008807
68. 47355105 c.3190+3G>A splice site 0.00000845
69. 47355104 c.3190+4C>T splice site 0.00009315
70. 47355103 c.3190+5G>A splice site 0.00001696
71. 47354888 c.3191-4G>A splice site 0.00003027
72. 47354740 c.3330+5G>C splice site 0.00003052
73. 47354362 c.3490+3_3490+7delGCTGT splice site 0.00001488
74. 47354362 c.3490+3G>A splice site 0.00001461
75. 47354359 c.3490+6G>A splice site 0.00001476
76. 47354252 c.3492C>T splice site 0.00001211
77. 47353814 c.3628-5T>C splice site 0.00000832
78. 47353813 c.3628-4A>G splice site 0.00000832
79. 47353624 c.3813A>G splice site 0.00000859
80. 47353440 c.3815-8T>C splice site 0.00001075
81. 47353431 c.3816G>A splice site 0.00001086
82. 47353398 c.*24C>A splice site 0.00002350
83. 0 c.506-12delC splice site 0.68791751
84. 0 c.*26+8C>T splice site 0.00001197
85. 0 c.906-12_906-11insCTG splice site 0.00001792

* 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.