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