NF1 splice variants in ExAC


The table below lists the NF1 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. 29663499 c.6084+8C>G splice site 0.00142751
2. 29560021 c.3498C>T p.G1166G splice site 0.00124440
3. 29587544 c.4514+11C>G splice site 0.00088986
4. 29585352 c.4111-10_4111-8delTTG splice site 0.00055276
5. 29509520 c.731-6A>C splice site 0.00035902
6. 29663502 c.6084+11T>C splice site 0.00019809
7. 29665168 c.6756+11C>T splice site 0.00010711
8. 29509688 c.888+5G>A splice site 0.00009493
9. 29557945 c.3197+2_3197+3insA splice site 0.00007886
10. 29664383 c.6365-3C>T splice site 0.00006858
11. 29562621 c.3709-8G>C splice site 0.00005769
12. 29557274 c.2991-4A>G splice site 0.00005022
13. 29663499 c.6084+8C>T splice site 0.00004126
14. 29533394 c.1392+5G>T splice site 0.00004120
15. 29533395 c.1392+6A>T splice site 0.00004120
16. 29665161 c.6756+4C>T splice site 0.00004119
17. 29528425 c.1186-4A>G splice site 0.00003371
18. 29575998 c.3975-4G>A splice site 0.00003332
19. 29554629 c.2409+5G>C splice site 0.00003320
20. 29528052 c.1063-3T>C splice site 0.00003317
21. 29677344 c.7394+8G>T splice site 0.00003299
22. 29576141 c.4110+4T>C splice site 0.00003295
23. 29676131 c.7127-7T>G splice site 0.00002863
24. 29676133 c.7127-5T>C splice site 0.00002823
25. 29676139 c.7128G>A splice site 0.00002573
26. 29559715 c.3315-3C>T splice site 0.00002497
27. 29559907 c.3496+8C>T splice site 0.00002480
28. 29652835 c.4773-3T>C splice site 0.00002479
29. 29684279 c.7807-8C>A splice site 0.00002474
30. 29562932 c.3871-4G>C splice site 0.00002472
31. 29665164 c.6756+7G>C splice site 0.00002471
32. 29509691 c.888+8G>A splice site 0.00001919
33. 29546144 c.1641+8G>A splice site 0.00001893
34. 29685490 c.7908-8T>C splice site 0.00001728
35. 29664906 c.6641+8C>T splice site 0.00001723
36. 29670161 c.7126+8A>G splice site 0.00001685
37. 29670155 c.7126+2_7126+3insA splice site 0.00001679
38. 29557278 c.2991G>A splice site 0.00001672
39. 29559710 c.3315-8T>C splice site 0.00001670
40. 29662053 c.5943+4T>C splice site 0.00001665
41. 29663345 c.5944-6A>G splice site 0.00001659
42. 29685980 c.8051-7G>A splice site 0.00001656
43. 29490401 c.479+7G>A splice site 0.00001656
44. 29508725 c.655-3T>C splice site 0.00001654
45. 29701027 c.8315-4C>T splice site 0.00001652
46. 29554532 c.2326-9T>A splice site 0.00001651
47. 29679268 c.7395-7C>T splice site 0.00001650
48. 29576140 c.4110+3A>G splice site 0.00001648
49. 29533389 c.1392G>A p.P464P splice site 0.00001648
50. 29562925 c.3871-11C>T splice site 0.00001648
51. 29533260 c.1263C>T splice site 0.00001648
52. 29562932 c.3871-4G>A splice site 0.00001648
53. 29677202 c.7260T>G splice site 0.00001648
54. 29557854 c.3114-6C>T splice site 0.00000991
55. 29557854 c.3114-6C>G splice site 0.00000991
56. 29557856 c.3114-4A>G splice site 0.00000983
57. 29679439 c.7552+7T>C splice site 0.00000944
58. 29548951 c.1721+4T>A splice site 0.00000934
59. 29546139 c.1641+3A>G splice site 0.00000931
60. 29546139 c.1641+3delA splice site 0.00000929
61. 29497023 c.586+8T>C splice site 0.00000888
62. 29654508 c.5206-9A>G splice site 0.00000859
63. 29657524 c.5749+8A>G splice site 0.00000858
64. 29664901 c.6641+3A>G splice site 0.00000857
65. 29541610 c.1527+7_1527+8insT splice site 0.00000853
66. 29664829 c.6580-8T>A splice site 0.00000847
67. 29528423 c.1186-6C>A splice site 0.00000844
68. 29653277 c.5205+7T>C splice site 0.00000844
69. 29528423 c.1186-6C>T splice site 0.00000844
70. 29670160 c.7126+7A>G splice site 0.00000841
71. 29528431 c.1188C>T splice site 0.00000841
72. 29670157 c.7126+4A>C splice site 0.00000840
73. 29490197 c.289-7A>G splice site 0.00000838
74. 29508437 c.587-3C>T splice site 0.00000837
75. 29490198 c.289-6T>C splice site 0.00000837
76. 29662055 c.5943+6G>T splice site 0.00000833
77. 29592240 c.4662-7C>T splice site 0.00000833
78. 29557398 c.3111T>C p.F1037F splice site 0.00000832
79. 29556491 c.2850+8G>A splice site 0.00000832
80. 29592247 c.4662G>A p.R1554R splice site 0.00000832
81. 29556489 c.2850+6G>A splice site 0.00000832
82. 29554628 c.2409+4A>G splice site 0.00000830
83. 29486115 c.288+4A>C splice site 0.00000830
84. 29663348 c.5944-3T>C splice site 0.00000828
85. 29665827 c.6858+4A>G splice site 0.00000827
86. 29508720 c.655-8A>G splice site 0.00000827
87. 29508723 c.655-5T>C splice site 0.00000827
88. 29654865 c.5546+8T>C splice site 0.00000827
89. 29665828 c.6858+5T>C splice site 0.00000827
90. 29670019 c.7000-8delT splice site 0.00000826
91. 29550459 c.1722-3C>T splice site 0.00000826
92. 29588878 c.4661+3A>G splice site 0.00000826
93. 29687498 c.8098-7A>G splice site 0.00000826
94. 29701025 c.8315-6C>T splice site 0.00000826
95. 29585357 c.4111-5T>C splice site 0.00000825
96. 29588721 c.4515-8G>A splice site 0.00000825
97. 29670021 c.7000-6T>C splice site 0.00000825
98. 29588724 c.4515-5T>C splice site 0.00000825
99. 29657307 c.5547-7C>T splice site 0.00000825
100. 29683474 c.7553-4A>G splice site 0.00000825
101. 29670023 c.7000-4A>G splice site 0.00000825
102. 29562797 c.3870+7A>G splice site 0.00000824
103. 29587387 c.4368G>A p.R1456R splice site 0.00000824
104. 29533255 c.1261-3T>A splice site 0.00000824
105. 29483151 c.204+7A>G splice site 0.00000824
106. 29576140 c.4110+3A>C splice site 0.00000824
107. 29683975 c.7676-3C>T splice site 0.00000824
108. 29533396 c.1392+7T>C splice site 0.00000824
109. 29667515 c.6859-8T>C 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.