LAMA4 splice variants in ExAC


The table below lists the LAMA4 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. 112435273 c.5305+6T>G splice site 0.23923374
2. 112463321 c.2646C>T p.N882N splice site 0.00001649
3. 112496511 c.1336+4G>T splice site 0.03149717
4. 112496690 c.1169-8C>G splice site 0.00961665
5. 112522893 c.423-4T>G splice site 0.01335667
6. 112453955 c.3813G>A p.G1271G splice site 0.00002515
7. 112476147 c.1941G>A p.A647A splice site 0.00026388
8. 112476767 c.1938T>C p.D646D splice site 0.00103001
9. 112439104 c.4801-3C>T splice site 0.00050451
10. 112441478 c.4644+8G>T splice site 0.00035587
11. 112454696 c.3537-7T>C splice site 0.00010717
12. 112493809 c.1530+4C>T splice site 0.00008246
13. 112537561 c.297+8G>A splice site 0.00032998
14. 112437058 c.5091+8C>T splice site 0.00000824
15. 112457459 c.3262-3C>G splice site 0.00016515
16. 112461954 c.2955+8A>G splice site 0.00000844
17. 112462553 c.2792+7T>C splice site 0.00000824
18. 112471706 c.2152+7A>T splice site 0.00000824
19. 112476152 c.1939-3T>C splice site 0.00003299
20. 112486482 c.1531-4G>A splice site 0.00002471
21. 112493806 c.1530+7C>A splice site 0.00000825
22. 112494013 c.1337-7T>C splice site 0.00001755
23. 112499315 c.1168+8T>C splice site 0.00004127
24. 112510411 c.719-4A>G splice site 0.00004177
25. 112512833 c.718+5A>G splice site 0.00000850
26. 112437199 c.4961-3delC splice site 0.00001652
27. 112463319 c.2646+2dupT splice site 0.00000825
28. 112480089 c.1648-7delT splice site 0.00019425
29. 112435858 c.5185+8A>G splice site 0.00000826
30. 112437062 c.5091+4G>A splice site 0.00001648
31. 112452165 c.3947+5A>G splice site 0.00000826
32. 112454095 c.3676-3C>T splice site 0.00000826
33. 0 c.2956-12delT splice site 0.00021476
34. 112486353 c.1647+9G>A splice site 0.00010710
35. 112486354 c.1647+8C>T splice site 0.00009062
36. 112522899 c.423-10C>T splice site 0.00461495
37. 112537679 c.196-9C>T splice site 0.00044286
38. 112435273 c.5305+6T>A splice site 0.00000825
39. 112435273 c.5305+6T>C splice site 0.00001650
40. 112435403 c.5186-5T>C splice site 0.00000826
41. 112435861 c.5185+5G>T splice site 0.00000826
42. 112437202 c.4961-6C>T splice site 0.00000827
43. 112440351 c.4800+8A>G splice site 0.00000826
44. 112441479 c.4644+7T>C splice site 0.00000827
45. 112441679 c.4455-4C>A splice site 0.00002582
46. 112443210 c.4454+7T>G splice site 0.00000825
47. 112443407 c.4267-3T>C splice site 0.00002496
48. 112450118 c.4266+6A>G splice site 0.00000828
49. 112450120 c.4266+4A>G splice site 0.00004140
50. 112451249 c.3948-7T>C splice site 0.00000827
51. 112453952 c.3813+3_3813+6delAAGT splice site 0.00000842
52. 112453950 c.3813+5G>A splice site 0.00000841
53. 112454100 c.3676-8G>A splice site 0.00000826
54. 112454543 c.3675+8C>T splice site 0.00003297
55. 112454543 c.3675+8C>A splice site 0.00000824
56. 112454689 c.3537G>A splice site 0.00000824
57. 112455663 c.3536+6G>A splice site 0.00001652
58. 112455663 c.3536+6G>C splice site 0.00000826
59. 112457318 c.3393+7delA splice site 0.00000826
60. 112457461 c.3262-5C>G splice site 0.00000826
61. 112460315 c.3261+7A>G splice site 0.00001648
62. 112462128 c.2793-4delA splice site 0.00000827
63. 112462128 c.2793-4A>G splice site 0.00000827
64. 112462711 c.2647-6T>C splice site 0.00000833
65. 112462713 c.2647-8T>C splice site 0.00001670
66. 112463313 c.2646+8C>T splice site 0.00000825
67. 112463500 c.2473-6C>T splice site 0.00001649
68. 112463502 c.2473-8C>T splice site 0.00000824
69. 112469544 c.2153-6G>A splice site 0.00000825
70. 112471705 c.2152+8T>A splice site 0.00001648
71. 112476048 c.2035+5A>G splice site 0.00000824
72. 112476761 c.1938+6T>C splice site 0.00000824
73. 112476764 c.1938+3G>C splice site 0.00001648
74. 112476764 c.1938+3G>A splice site 0.00000824
75. 112476916 c.1797-8A>G splice site 0.00002473
76. 112480085 c.1648-3T>C splice site 0.00000912
77. 112480086 c.1648-4T>C splice site 0.00000912
78. 112486483 c.1531-5C>T splice site 0.00000824
79. 112493805 c.1530+8G>A splice site 0.00023092
80. 112493806 c.1530+7C>T splice site 0.00002474
81. 112496508 c.1336+7G>A splice site 0.00001648
82. 112496512 c.1336+3A>G splice site 0.00000824
83. 112506434 c.1056+5G>A splice site 0.00003295
84. 112508647 c.945+5G>A splice site 0.00000824
85. 112508648 c.945+4C>A splice site 0.00001648
86. 112510327 c.793+6G>A splice site 0.00000828
87. 112510327 c.793+6G>T splice site 0.00000828
88. 112510334 c.792A>C splice site 0.00000827
89. 112510406 c.720G>A splice site 0.00001665
90. 112512832 c.718+6G>T splice site 0.00003405
91. 112513052 c.504A>G splice site 0.00000901
92. 112537677 c.196-7G>A splice site 0.00000835
93. 112575153 c.195+5A>G splice site 0.00001458

* 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.