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

* 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.