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

* 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.