DTNA non-truncating variants in ExAC


The table below lists the DTNA non-truncating variants found in the ExAC population database with a mean allelic frequency (MAF) less than 0.0001, classified for this study as a rare variant. 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. 32335947 c.7G>A p.E3K missense 0.00000854
2. 32335951 c.11A>G p.D4G missense 0.00000850
3. 32335977 c.37G>A p.A13T missense 0.00000844
4. 32335982 c.42A>C p.E14D missense 0.00000844
5. 32345927 c.70G>T p.A24S missense 0.00001659
6. 32345942 c.85C>T p.R29C missense 0.00003311
7. 32345949 c.92G>C p.R31P missense 0.00000827
8. 32345969 c.112G>A p.A38T missense 0.00000827
9. 32374003 c.151C>T p.H51Y missense 0.00000906
10. 32374005 c.153C>G p.H51Q missense 0.00000893
11. 32374006 c.154C>G p.L52V missense 0.00000888
12. 32374009 c.157G>A p.V53M missense 0.00000874
13. 32374014 c.162C>A p.D54E missense 0.00000859
14. 32374018 c.166T>A p.W56R missense 0.00000849
15. 32374024 c.172G>T p.V58F missense 0.00001681
16. 32374028 c.176T>C p.I59T missense 0.00000836
17. 32374034 c.182C>G p.A61G missense 0.00002496
18. 32374039 c.187C>T p.R63W missense 0.00000830
19. 32374040 c.188G>A p.R63Q missense 0.00003317
20. 32374049 c.197C>T p.A66V missense 0.00000827
21. 32374058 c.206A>C p.N69T missense 0.00000826
22. 32374065 c.213C>G p.D71E missense 0.00000825
23. 32374082 c.230A>G p.N77S missense 0.00000824
24. 32374083 c.231C>G p.N77K missense 0.00000824
25. 32374088 c.236C>G p.S79C missense 0.00001649
26. 32374090 c.238C>T p.R80C missense 0.00001649
27. 32374091 c.239G>A p.R80H missense 0.00007419
28. 32374099 c.247G>T p.A83S missense 0.00000824
29. 32374100 c.248C>T p.A83V missense 0.00000824
30. 32374102 c.250G>A p.V84M missense 0.00000824
31. 32374111 c.259A>G p.T87A missense 0.00000824
32. 32374132 c.280A>G p.K94E missense 0.00000824
33. 32374144 c.292A>G p.T98A missense 0.00000824
34. 32374147 c.295A>G p.T99A missense 0.00001648
35. 32374169 c.317A>T p.Q106L missense 0.00000824
36. 32374204 c.352G>A p.A118T missense 0.00001648
37. 32374214 c.362C>T p.P121L missense 0.00000824
38. 32386210 c.390T>G p.F130L missense 0.00001656
39. 32386232 c.412A>G p.T138A missense 0.00003312
40. 32386249 c.429G>T p.K143N missense 0.00000831
41. 32386255 c.435G>A p.M145I missense 0.00000833
42. 32391931 c.457T>C p.S153P missense 0.00000826
43. 32391950 c.476G>A p.S159N missense 0.00007428
44. 32391956 c.482T>C p.V161A missense 0.00003300
45. 32391958 c.484A>G p.M162V missense 0.00000825
46. 32391971 c.497G>A p.R166Q missense 0.00003299
47. 32391989 c.515G>A p.R172Q missense 0.00003299
48. 32391994 c.520G>A p.V174I missense 0.00000825
49. 32392009 c.535A>G p.T179A missense 0.00000824
50. 32392010 c.536C>T p.T179M missense 0.00000824
51. 32392012 c.538G>A p.A180T missense 0.00000824
52. 32392027 c.553C>T p.P185S missense 0.00000825
53. 32395883 c.614C>T p.T205M missense 0.00009066
54. 32395903 c.634A>G p.T212A missense 0.00000824
55. 32395911 c.642G>A p.M214I missense 0.00001648
56. 32395915 c.646G>T p.D216Y missense 0.00000824
57. 32395919 c.650C>T p.P217L missense 0.00000824
58. 32395925 c.656C>T p.P219L missense 0.00000824
59. 32395936 c.667G>A p.V223I missense 0.00000824
60. 32395964 c.695C>T p.A232V missense 0.00000824
61. 32398137 c.719C>T p.P240L missense 0.00000824
62. 32398172 c.754A>G p.M252V missense 0.00001648
63. 32398188 c.770G>A p.R257Q missense 0.00001648
64. 32398202 c.784C>T p.H262Y missense 0.00003296
65. 32398204 c.786C>A p.H262Q missense 0.00000824
66. 32398205 c.787A>T p.N263Y missense 0.00000824
67. 32398220 c.802C>G p.Q268E missense 0.00000824
68. 32398242 c.824A>G p.H275R missense 0.00000826
69. 32398278 c.860A>G p.K287R missense 0.00000844
70. 32398287 c.869C>T p.T290M missense 0.00005166
71. 32400761 c.883C>T p.P295S missense 0.00000824
72. 32400768 c.890A>G p.K297R missense 0.00000824
73. 32400782 c.904G>A p.A302T missense 0.00003295
74. 32400782 c.904G>T p.A302S missense 0.00000824
75. 32400810 c.932C>G p.S311C missense 0.00000824
76. 32400815 c.937C>T p.R313C missense 0.00001648
77. 32400815 c.937C>A p.R313S missense 0.00000824
78. 32400816 c.938G>A p.R313H missense 0.00000824
79. 32400822 c.944C>G p.P315R missense 0.00000824
80. 32400840 c.962C>T p.P321L missense 0.00000824
81. 32400847 c.969G>C p.Q323H missense 0.00004119
82. 32400860 c.982C>T p.L328F missense 0.00000824
83. 32400861 c.983T>A p.L328H missense 0.00000824
84. 32400867 c.989T>G p.L330W missense 0.00000824
85. 32400872 c.994C>T p.H332Y missense 0.00000824
86. 32400873 c.995A>G p.H332R missense 0.00000824
87. 32400875 c.997A>G p.I333V missense 0.00001648
88. 32407583 c.1028A>T p.N343I missense 0.00000824
89. 32407585 c.1030G>A p.D344N missense 0.00001647
90. 32407604 c.1049C>T p.S350F missense 0.00000824
91. 32407607 c.1052T>A p.V351D missense 0.00000824
92. 32407621 c.1066A>G p.S356G missense 0.00000824
93. 32407630 c.1075A>G p.I359V missense 0.00000824
94. 32407637 c.1082G>A p.R361K missense 0.00000824
95. 32418065 c.1093C>T p.P365S missense 0.00005815
96. 32418075 c.1103G>A p.S368N missense 0.00000829
97. 32418092 c.1120A>G p.K374E missense 0.00000828
98. 32418101 c.1129G>T p.A377S missense 0.00003313
99. 32418110 c.1138G>A p.A380T missense 0.00000829
100. 32418110 c.1138G>T p.A380S missense 0.00000829
101. 32418119 c.1147T>G p.F383V missense 0.00000829
102. 32418714 c.1169A>G p.Q390R missense 0.00000824
103. 32418725 c.1180A>G p.N394D missense 0.00004945
104. 32418744 c.1199C>T p.A400V missense 0.00000824
105. 32418746 c.1201G>A p.D401N missense 0.00000824
106. 32418758 c.1213C>A p.L405I missense 0.00000824
107. 32418764 c.1219G>A p.G407R missense 0.00001649
108. 32418765 c.1220G>C p.G407A missense 0.00000825
109. 32418777 c.1232A>G p.N411S missense 0.00001649
110. 32418779 c.1234A>G p.M412V missense 0.00000825
111. 32418785 c.1240C>T p.R414W missense 0.00004950
112. 32418786 c.1241G>A p.R414Q missense 0.00000825
113. 32418800 c.1255T>C p.C419R missense 0.00004131
114. 32418800 c.1255T>A p.C419S missense 0.00000826
115. 32428268 c.1265A>G p.E422G missense 0.00000827
116. 32428279 c.1276C>T p.R426W missense 0.00000826
117. 32428280 c.1277G>A p.R426Q missense 0.00000826
118. 32428310 c.1307G>C p.R436T missense 0.00001652
119. 32428313 c.1310A>G p.Y437C missense 0.00003304
120. 32428316 c.1313C>T p.A438V missense 0.00000826
121. 32428337 c.1334C>T p.S445F missense 0.00000828
122. 32428343 c.1340C>T p.S447L missense 0.00000829
123. 32431804 c.1354C>G p.Q452E missense 0.00000826
124. 32431805 c.1355A>G p.Q452R missense 0.00000826
125. 32431823 c.1373A>G p.D458G missense 0.00000825
126. 32431837 c.1387A>G p.I463V missense 0.00001650
127. 32431840 c.1390G>A p.D464N missense 0.00006601
128. 32431844 c.1394C>T p.A465V missense 0.00000825
129. 32431858 c.1408A>T p.R470W missense 0.00001652
130. 32431891 c.1441A>G p.R481G missense 0.00000833
131. 32438251 c.1445A>G p.E482G missense 0.00000847
132. 32438277 c.1471C>T p.R491W missense 0.00000832
133. 32438281 c.1475T>G p.L492R missense 0.00000830
134. 32438285 c.1479G>C p.E493D missense 0.00000830
135. 32438313 c.1507G>C p.E503Q missense 0.00000828
136. 32438314 c.1508A>T p.E503V missense 0.00000828
137. 32438319 c.1513G>A p.A505T missense 0.00000828
138. 32438329 c.1523A>G p.N508S missense 0.00000829
139. 32438335 c.1529C>T p.T510I missense 0.00000830
140. 32438352 c.1546C>T p.R516W missense 0.00000834
141. 32438355 c.1549C>T p.L517F missense 0.00000835
142. 32443954 c.1581G>C p.Q527H missense 0.00001056
143. 32446088 c.1667A>G p.K556R missense 0.00000824
144. 32446093 c.1672G>A p.G558R missense 0.00001648

* 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.