ANKRD1 non-truncating variants in ExAC


The table below lists the ANKRD1 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. 92680784 c.1A>G p.Met1? missense 0.00000825
2. 92680783 c.2T>A p.Met1? missense 0.00000825
3. 92680783 c.2T>G p.Met1? missense 0.00000825
4. 92680780 c.5T>C p.M2T missense 0.00001651
5. 92680105 c.28G>A p.V10I missense 0.00003296
6. 92680090 c.43A>C p.N15H missense 0.00001648
7. 92680081 c.52G>A p.G18R missense 0.00000824
8. 92680080 c.53G>C p.G18A missense 0.00000824
9. 92680074 c.59C>T p.A20V missense 0.00000824
10. 92680074 c.59C>A p.A20E missense 0.00000824
11. 92680060 c.73C>T p.P25S missense 0.00000824
12. 92680048 c.85A>G p.R29G missense 0.00000824
13. 92680041 c.92G>A p.G31E missense 0.00000824
14. 92680029 c.104C>T p.A35V missense 0.00000824
15. 92680026 c.107C>T p.A36V missense 0.00000824
16. 92680023 c.110T>C p.V37A missense 0.00000824
17. 92680020 c.113C>T p.T38I missense 0.00000824
18. 92680002 c.131A>G p.D44G missense 0.00002471
19. 92680001 c.132T>A p.D44E missense 0.00004942
20. 92680000 c.133C>G p.L45V missense 0.00001647
21. 92679999 c.134T>A p.L45Q missense 0.00000824
22. 92679979 c.154C>T p.P52S missense 0.00000824
23. 92679952 c.181A>G p.K61E missense 0.00000824
24. 92679946 c.187G>A p.E63K missense 0.00005766
25. 92679939 c.194_196delAAC p.Q65_R66delinsR inframe 0.00000824
26. 92679939 c.194A>C p.Q65P missense 0.00000824
27. 92678999 c.234A>T p.R78S missense 0.00006260
28. 92678976 c.257A>G p.D86G missense 0.00000875
29. 92678974 c.259C>T p.L87F missense 0.00000873
30. 92678973 c.260T>A p.L87H missense 0.00000873
31. 92678962 c.271A>G p.I91V missense 0.00000862
32. 92678949 c.284A>G p.K95R missense 0.00000851
33. 92678729 c.346A>G p.T116A missense 0.00000861
34. 92678717 c.358G>A p.D120N missense 0.00000831
35. 92678711 c.364C>G p.P122A missense 0.00001659
36. 92678710 c.365C>T p.P122L missense 0.00001655
37. 92678675 c.400C>T p.P134S missense 0.00001652
38. 92678626 c.449A>T p.D150V missense 0.00009082
39. 92678626 c.449A>G p.D150G missense 0.00000826
40. 92677583 c.458A>C p.K153T missense 0.00000828
41. 92677581 c.460C>T p.R154W missense 0.00000828
42. 92677580 c.461G>A p.R154Q missense 0.00000828
43. 92677575 c.466G>A p.A156T missense 0.00000827
44. 92677569 c.472C>T p.H158Y missense 0.00000826
45. 92677565 c.476G>C p.R159T missense 0.00002478
46. 92677565 c.476G>T p.R159I missense 0.00000826
47. 92677563 c.478G>A p.A160T missense 0.00000826
48. 92677533 c.508G>A p.E170K missense 0.00000825
49. 92677514 c.527G>A p.G176E missense 0.00000825
50. 92677512 c.529G>A p.A177T missense 0.00000825
51. 92677503 c.538G>A p.E180K missense 0.00000825
52. 92677497 c.544C>T p.R182C missense 0.00000826
53. 92676009 c.570C>G p.I190M missense 0.00000827
54. 92675996 c.583C>T p.R195C missense 0.00001651
55. 92675995 c.584G>C p.R195P missense 0.00000826
56. 92675954 c.625G>C p.G209R missense 0.00001650
57. 92675939 c.640G>A p.A214T missense 0.00000826
58. 92675928 c.651G>T p.K217N missense 0.00001655
59. 92675634 c.655C>T p.L219F missense 0.00001703
60. 92675631 c.658A>C p.S220R missense 0.00000845
61. 92675622 c.667C>A p.L223M missense 0.00000836
62. 92675619 c.670C>T p.H224Y missense 0.00000834
63. 92675613 c.676G>C p.A226P missense 0.00000832
64. 92675592 c.697G>C p.E233Q missense 0.00000828
65. 92675586 c.703G>A p.A235T missense 0.00000826
66. 92675583 c.706G>A p.E236K missense 0.00000826
67. 92675579 c.710A>G p.H237R missense 0.00002476
68. 92675573 c.716T>C p.I239T missense 0.00000825
69. 92675571 c.718G>C p.A240P missense 0.00000825
70. 92675570 c.719C>T p.A240V missense 0.00000825
71. 92675567 c.722G>A p.C241Y missense 0.00001649
72. 92675561 c.728C>G p.A243G missense 0.00001649
73. 92675559 c.730G>C p.D244H missense 0.00000824
74. 92675553 c.736A>G p.N246D missense 0.00001649
75. 92675550 c.739G>A p.A247T missense 0.00000824
76. 92675385 c.764C>T p.P255L missense 0.00000825
77. 92675364 c.785T>G p.L262R missense 0.00000825
78. 92675355 c.794A>G p.Y265C missense 0.00001650
79. 92675353 c.796A>G p.K266E missense 0.00000825
80. 92675343 c.806G>A p.R269Q missense 0.00002475
81. 92675338 c.811C>A p.L271M missense 0.00000825
82. 92675331 c.818T>C p.M273T missense 0.00009082
83. 92675330 c.819G>A p.M273I missense 0.00000826
84. 92675329 c.820T>C p.Y274H missense 0.00003303
85. 92675328 c.821A>G p.Y274C missense 0.00001652
86. 92675311 c.838A>G p.I280V missense 0.00003316
87. 92672732 c.851C>G p.A284G missense 0.00000824
88. 92672712 c.871C>A p.L291M missense 0.00000824
89. 92672709 c.874G>C p.V292L missense 0.00000824
90. 92672702 c.881A>G p.H294R missense 0.00002471
91. 92672687 c.896C>A p.T299N missense 0.00000824
92. 92672678 c.905T>C p.I302T missense 0.00001647
93. 92672676 c.907T>C p.F303L missense 0.00000824
94. 92672675 c.908T>G p.F303C missense 0.00001647
95. 92672656 c.927C>A p.N309K missense 0.00000824
96. 92672654 c.929_931delCCT p.Ser310del inframe 0.00000824
97. 92672649 c.934A>G p.K312E missense 0.00000824
98. 92672640 c.943C>T p.R315C missense 0.00000824
99. 92672639 c.944G>A p.R315H missense 0.00005766
100. 92672639 c.944G>T p.R315L missense 0.00001647
101. 92672636 c.947T>C p.I316T missense 0.00001647
102. 92672634 c.949G>C p.A317P missense 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.