FHL2 missense variants in ExAC


The table below lists the FHL2 missense 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. 106002970 c.4A>G p.T2A missense 0.00001654
2. 106002964 c.10C>T p.R4C missense 0.00002478
3. 106002964 c.10C>A p.R4S missense 0.00002478
4. 106002963 c.11G>A p.R4H missense 0.00000826
5. 106002957 c.17A>G p.D6G missense 0.00000825
6. 106002948 c.26A>G p.H9R missense 0.00000825
7. 106002946 c.28T>C p.C10R missense 0.00000825
8. 106002940 c.34G>A p.E12K missense 0.00000824
9. 106002939 c.35A>G p.E12G missense 0.00000824
10. 106002937 c.37T>A p.S13T missense 0.00001649
11. 106002919 c.55T>C p.Y19H missense 0.00000824
12. 106002918 c.56A>T p.Y19F missense 0.00001648
13. 106002912 c.62T>A p.L21Q missense 0.00001648
14. 106002912 c.62T>G p.L21R missense 0.00000824
15. 106002910 c.64C>T p.R22W missense 0.00001648
16. 106002902 c.72G>C p.E24D missense 0.00002472
17. 106002889 c.85G>A p.V29M missense 0.00107966
18. 106002865 c.109G>T p.A37S missense 0.00058551
19. 106002865 c.109G>A p.A37T missense 0.00004948
20. 106002861 c.113A>G p.N38S missense 0.00000825
21. 106002858 c.116C>T p.T39I missense 0.00000825
22. 106002853 c.121G>A p.E41K missense 0.00002476
23. 106002852 c.122A>G p.E41G missense 0.00000825
24. 106002846 c.128G>T p.C43F missense 0.00000826
25. 106002844 c.130G>A p.G44R missense 0.00000826
26. 106002832 c.142G>A p.G48S missense 0.00002483
27. 106002832 c.142G>C p.G48R missense 0.00000828
28. 106002820 c.154A>G p.K52E missense 0.00000831
29. 106002819 c.155A>G p.K52R missense 0.00001662
30. 105990190 c.157G>A p.D53N missense 0.00000827
31. 105990172 c.175C>T p.R59W missense 0.00002475
32. 105990171 c.176G>A p.R59Q missense 0.00000825
33. 105990164 c.183G>T p.W61C missense 0.00000825
34. 105990156 c.191C>T p.A64V missense 0.00000824
35. 105990156 c.191C>G p.A64G missense 0.00000824
36. 105990154 c.193T>C p.C65R missense 0.00002473
37. 105990139 c.208C>G p.Q70E missense 0.00012360
38. 105990114 c.233A>G p.K78R missense 0.00000824
39. 105990112 c.235C>G p.P79A missense 0.00002472
40. 105990111 c.236C>G p.P79R missense 0.00001648
41. 105990111 c.236C>T p.P79L missense 0.00000824
42. 105990072 c.275G>A p.C92Y missense 0.00000824
43. 105990066 c.281C>T p.S94F missense 0.00001648
44. 105990062 c.285C>G p.N95K missense 0.00003297
45. 105990052 c.295T>A p.S99T missense 0.00000824
46. 105984191 c.337C>T p.R113C missense 0.00038489
47. 105984190 c.338G>T p.R113L missense 0.00001673
48. 105984190 c.338G>A p.R113H missense 0.00002510
49. 105984188 c.340A>G p.K114E missense 0.00000836
50. 105984176 c.352A>C p.K118Q missense 0.00001659
51. 105984166 c.362G>A p.S121N missense 0.00000827
52. 105984155 c.373A>T p.T125S missense 0.00000825
53. 105984154 c.374C>A p.T125N missense 0.00000825
54. 105984137 c.391C>A p.R131S missense 0.00000826
55. 105984136 c.392G>A p.R131H missense 0.00004956
56. 105984126 c.402G>C p.Q134H missense 0.00013183
57. 105984124 c.404C>A p.P135Q missense 0.00000824
58. 105984122 c.406A>T p.I136F missense 0.00000824
59. 105984098 c.430A>G p.K144E missense 0.00000824
60. 105984067 c.461A>G p.Y154C missense 0.00001650
61. 105984050 c.478A>G p.M160V missense 0.00000829
62. 105984041 c.487G>A p.V163I missense 0.00002508
63. 105979921 c.509C>T p.T170I missense 0.00001290
64. 105979918 c.512C>T p.T171M missense 0.00006295
65. 105979909 c.521T>C p.V174A missense 0.00002356
66. 105979909 c.521T>A p.V174D missense 0.00002356
67. 105979907 c.523A>C p.T175P missense 0.00018435
68. 105979901 c.529C>T p.R177W missense 0.00002235
69. 105979900 c.530G>A p.R177Q missense 0.00538927
70. 105979898 c.532G>A p.E178K missense 0.00001094
71. 105979871 c.559G>T p.V187L missense 0.00023145
72. 105979871 c.559G>A p.V187M missense 0.00003858
73. 105979837 c.593A>G p.Q198R missense 0.00000866
74. 105979835 c.595C>T p.R199C missense 0.00002585
75. 105979798 c.632A>T p.N211I missense 0.00000830
76. 105979798 c.632A>G p.N211S missense 0.00000830
77. 105979789 c.641G>A p.C214Y missense 0.00000829
78. 105979786 c.644A>C p.D215A missense 0.00000829
79. 105979775 c.655A>C p.K219Q missense 0.00000828
80. 105979762 c.668G>T p.G223V missense 0.00000828
81. 105979742 c.688G>A p.G230R missense 0.00008307
82. 105977891 c.689G>T p.G230V missense 0.00001651
83. 105977856 c.724C>T p.R242W missense 0.00001648
84. 105977855 c.725G>A p.R242Q missense 0.00002472
85. 105977855 c.725G>C p.R242P missense 0.00000824
86. 105977841 c.739G>A p.D247N missense 0.00005767
87. 105977830 c.750C>G p.N250K missense 0.00003295
88. 105977824 c.756G>C p.K252N missense 0.00000824
89. 105977820 c.760T>G p.C254G missense 0.00000824
90. 105977802 c.778G>A p.G260R missense 0.00000824
91. 105977798 c.782G>A p.R261H missense 0.00003295
92. 105977786 c.794C>T p.T265I missense 0.00000824
93. 105977775 c.805G>A p.D269N missense 0.00001648
94. 105977775 c.805G>C p.D269H missense 0.00000824
95. 105977765 c.815G>A p.C272Y missense 0.00001649
96. 105977760 c.820G>A p.D274N missense 0.00002475
97. 105977759 c.821A>G p.D274G missense 0.00002475
98. 105977757 c.823T>C p.C275R missense 0.00000825
99. 105977756 c.824G>A p.C275Y missense 0.00000826

* 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.