CASQ2 non-truncating variants in ExAC


The table below lists the CASQ2 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. 116311155 c.8G>C p.R3T missense 0.00000865
2. 116311152 c.11C>T p.T4I missense 0.00000857
3. 116311148 c.15C>G p.H5Q missense 0.00000848
4. 116311145 c.18G>T p.L6F missense 0.00000845
5. 116311129 c.34T>A p.Y12N missense 0.00000832
6. 116311099 c.64G>A p.G22R missense 0.00000825
7. 116311098 c.65G>A p.G22E missense 0.00000825
8. 116311086 c.77C>T p.P26L missense 0.00000824
9. 116311083 c.80C>T p.T27I missense 0.00000824
10. 116311071 c.92A>G p.K31R missense 0.00000824
11. 116311065 c.98G>A p.R33Q missense 0.00000824
12. 116311060 c.103G>C p.V35L missense 0.00002472
13. 116311048 c.115G>A p.E39K missense 0.00004119
14. 116311030 c.133G>T p.V45F missense 0.00000824
15. 116311019 c.144A>C p.K48N missense 0.00003295
16. 116311018 c.145T>C p.Y49H missense 0.00000824
17. 116310990 c.173A>T p.E58V missense 0.00004942
18. 116310981 c.182C>T p.S61F missense 0.00000824
19. 116310951 c.212A>C p.Q71P missense 0.00000824
20. 116310950 c.213A>C p.Q71H missense 0.00000824
21. 116310934 c.229C>T p.L77F missense 0.00000824
22. 116287533 c.235C>T p.L79F missense 0.00000871
23. 116287523 c.245A>G p.Q82R missense 0.00000860
24. 116287511 c.257A>G p.H86R missense 0.00000851
25. 116287503 c.265A>G p.I89V missense 0.00000848
26. 116287499 c.269G>A p.G90D missense 0.00000846
27. 116287487 c.281T>C p.V94A missense 0.00001685
28. 116287479 c.289A>G p.K97E missense 0.00000841
29. 116283434 c.335G>A p.G112E missense 0.00001665
30. 116283432 c.337A>C p.S113R missense 0.00000831
31. 116283431 c.338G>A p.S113N missense 0.00004157
32. 116283408 c.361C>T p.R121C missense 0.00001652
33. 116283407 c.362G>A p.R121H missense 0.00002478
34. 116283402 c.367A>G p.I123V missense 0.00000826
35. 116283393 c.376G>C p.D126H missense 0.00000826
36. 116283389 c.380G>A p.G127D missense 0.00000826
37. 116283360 c.409T>C p.F137L missense 0.00001651
38. 116283356 c.413T>C p.L138P missense 0.00000826
39. 116280945 c.432C>G p.D144E missense 0.00000824
40. 116280944 c.433C>T p.P145S missense 0.00002471
41. 116280928 c.449G>T p.S150I missense 0.00000824
42. 116280913 c.464T>C p.V155A missense 0.00000824
43. 116280908 c.469G>C p.A157P missense 0.00001647
44. 116280902 c.475G>C p.E159Q missense 0.00000824
45. 116280899 c.478C>T p.R160C missense 0.00001647
46. 116280898 c.479G>A p.R160H missense 0.00003295
47. 116280896 c.481A>C p.I161L missense 0.00000824
48. 116280895 c.482T>C p.I161T missense 0.00001647
49. 116280889 c.488A>T p.D163V missense 0.00000824
50. 116280886 c.491A>G p.Y164C missense 0.00001647
51. 116280881 c.496A>C p.K166Q missense 0.00000824
52. 116280874 c.503T>C p.I168T missense 0.00001647
53. 116275595 c.533A>G p.Y178C missense 0.00000824
54. 116275587 c.541G>C p.A181P missense 0.00000824
55. 116275587 c.541G>A p.A181T missense 0.00000824
56. 116275581 c.547G>A p.E183K missense 0.00000824
57. 116275572 c.556G>A p.A186T missense 0.00000824
58. 116275565 c.563A>G p.H188R missense 0.00001648
59. 116275550 c.578T>A p.I193N missense 0.00000824
60. 116275547 c.581A>C p.K194T missense 0.00000824
61. 116275539 c.589G>T p.A197S missense 0.00000824
62. 116275523 c.605G>C p.G202A missense 0.00000824
63. 116269735 c.615G>T p.K205N missense 0.00002537
64. 116269728 c.622T>C p.S208P missense 0.00000842
65. 116269718 c.632T>C p.M211T missense 0.00000840
66. 116269717 c.633G>T p.M211I missense 0.00000839
67. 116269711 c.639G>C p.E213D missense 0.00000838
68. 116269710 c.640G>T p.V214F missense 0.00000838
69. 116269701 c.649T>C p.Y217H missense 0.00000836
70. 116269700 c.650A>G p.Y217C missense 0.00001671
71. 116269683 c.667G>A p.E223K missense 0.00000836
72. 116269677 c.673A>G p.I225V missense 0.00001673
73. 116269659 c.691C>A p.P231T missense 0.00000839
74. 116269658 c.692C>T p.P231L missense 0.00000840
75. 116269645 c.705G>T p.E235D missense 0.00000845
76. 116268173 c.739C>T p.P247S missense 0.00000841
77. 116268172 c.740C>G p.P247R missense 0.00000837
78. 116268172 c.740C>T p.P247L missense 0.00000837
79. 116268167 c.745C>G p.L249V missense 0.00000829
80. 116268164 c.748C>T p.R250C missense 0.00004961
81. 116268163 c.749G>T p.R250L missense 0.00000826
82. 116268163 c.749G>A p.R250H missense 0.00000826
83. 116268161 c.751C>T p.R251C missense 0.00000826
84. 116268160 c.752G>A p.R251H missense 0.00002487
85. 116268160 c.752G>T p.R251L missense 0.00000829
86. 116268155 c.757C>A p.R253S missense 0.00000825
87. 116268154 c.758G>A p.R253H missense 0.00008291
88. 116268148 c.764A>G p.E255G missense 0.00000825
89. 116260506 c.793T>G p.L265V missense 0.00000824
90. 116260490 c.809T>C p.I270T missense 0.00000824
91. 116260466 c.833A>G p.D278G missense 0.00000824
92. 116260464 c.835C>T p.P279S missense 0.00000824
93. 116247903 c.849A>C p.E283D missense 0.00001670
94. 116247892 c.860T>A p.I287N missense 0.00001655
95. 116247890 c.862C>G p.L288V missense 0.00000827
96. 116247883 c.869A>T p.Q290L missense 0.00003302
97. 116247882 c.870G>T p.Q290H missense 0.00000825
98. 116247877 c.875C>A p.A292D missense 0.00000825
99. 116247875 c.877C>T p.R293W missense 0.00004948
100. 116247874 c.878G>A p.R293Q missense 0.00003299
101. 116247869 c.883A>T p.N295Y missense 0.00000824
102. 116247868 c.884A>G p.N295S missense 0.00000824
103. 116247859 c.893A>G p.N298S missense 0.00006593
104. 116247854 c.898G>A p.D300N missense 0.00001648
105. 116247854 c.898G>T p.D300Y missense 0.00000824
106. 116247833 c.919G>A p.D307N missense 0.00001648
107. 116247829 c.923C>T p.P308L missense 0.00004119
108. 116247826 c.926A>G p.D309G missense 0.00000824
109. 116247826 c.926A>T p.D309V missense 0.00000824
110. 116247819 c.933T>A p.F311L missense 0.00000824
111. 116245613 c.943G>A p.V315I missense 0.00004837
112. 116245609 c.947C>T p.A316V missense 0.00002870
113. 116245607 c.949T>C p.Y317H missense 0.00000932
114. 116245585 c.971T>C p.I324T missense 0.00003556
115. 116245574 c.982A>G p.R328G missense 0.00001762
116. 116245568 c.988C>G p.Q330E missense 0.00002637
117. 116245565 c.991A>T p.I331F missense 0.00000879
118. 116244047 c.1015G>A p.A339T missense 0.00000861
119. 116244040 c.1022G>A p.S341N missense 0.00000852
120. 116244031 c.1031T>A p.M344K missense 0.00001684
121. 116244030 c.1032G>A p.M344I missense 0.00000842
122. 116244016 c.1046A>T p.D349V missense 0.00003333
123. 116244011 c.1051G>A p.D351N missense 0.00001661
124. 116244010 c.1052A>G p.D351G missense 0.00008304
125. 116243981 c.1081T>A p.W361R missense 0.00000826
126. 116243969 c.1093G>C p.V365L missense 0.00000825
127. 116243965 c.1097T>C p.L366P missense 0.00000825
128. 116243940 c.1122T>A p.D374E missense 0.00000825
129. 116243936 c.1126G>T p.D376Y missense 0.00000825
130. 116243934 c.1128_1130delTGA p.Asp376del inframe 0.00003305
131. 116243931 c.1131_1139delAGATGATGA p.Glu377_Asp379del inframe 0.00000825
132. 116243931 c.1131_1133delAGA p.Glu377del inframe 0.00000826
133. 116243928 c.1134T>A p.D378E missense 0.00000826
134. 116243917 c.1145A>G p.D382G missense 0.00000825
135. 116243916 c.1146_1147insGAT p.Asp383dup inframe 0.00003318
136. 116243914 c.1148A>G p.D383G missense 0.00009129
137. 116243912 c.1150A>C p.N384H missense 0.00000829
138. 116243897 c.1165G>T p.D389Y missense 0.00001651
139. 116243896 c.1166A>G p.D389G missense 0.00000825
140. 116243890 c.1172A>G p.D391G missense 0.00000825
141. 116243879 c.1183G>A p.D395N missense 0.00000825
142. 116243876 c.1186G>A p.D396N missense 0.00008381
143. 116243868 c.1194_1196dupTGA p.Asp398dup inframe 0.00000824
144. 116243866 c.1196A>C p.E399A 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.