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