CUL3 missense variants in ExAC


The table below lists the CUL3 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. 225362478 c.1699G>A p.V567I missense 0.12798027
2. 225376142 c.812A>G p.K271R missense 0.00018125
3. 225367719 c.1448C>T p.T483M missense 0.00015653
4. 225379383 c.485G>A p.R162Q missense 0.00008243
5. 225360560 c.1831T>A p.Y611N missense 0.00007486
6. 225422503 c.137G>A p.R46H missense 0.00006687
7. 225371682 c.922A>C p.N308H missense 0.00005786
8. 225449686 c.41C>A p.T14N missense 0.00003470
9. 225400352 c.271G>A p.E91K missense 0.00003406
10. 225367687 c.1480A>G p.T494A missense 0.00003296
11. 225378348 c.547A>G p.I183V missense 0.00002523
12. 225371694 c.910A>G p.S304G missense 0.00002484
13. 225370797 c.1082A>G p.N361S missense 0.00002479
14. 225365200 c.1490C>T p.S497F missense 0.00002473
15. 225342933 c.2159A>G p.N720S missense 0.00002472
16. 225376187 c.767C>T p.T256M missense 0.00002471
17. 225368517 c.1229C>T p.T410I missense 0.00002213
18. 225400346 c.277G>A p.V93I missense 0.00001695
19. 225400312 c.311C>T p.T104M missense 0.00001688
20. 225370788 c.1091G>A p.R364H missense 0.00001652
21. 225339047 c.2222T>C p.I741T missense 0.00001650
22. 225342973 c.2119A>G p.I707V missense 0.00001648
23. 225367734 c.1433G>C p.S478T missense 0.00001648
24. 225346665 c.1973T>C p.I658T missense 0.00001648
25. 225367715 c.1452G>C p.M484I missense 0.00001648
26. 225365093 c.1597G>C p.E533Q missense 0.00001648
27. 225449710 c.17A>G p.K6R missense 0.00001452
28. 225368381 c.1365A>G p.I455M missense 0.00001001
29. 225368483 c.1263T>G p.F421L missense 0.00000960
30. 225400277 c.346A>G p.M116V missense 0.00000878
31. 225400298 c.325T>G p.W109G missense 0.00000857
32. 225400354 c.269G>A p.R90Q missense 0.00000855
33. 225400312 c.311C>G p.T104R missense 0.00000844
34. 225422420 c.220T>C p.Y74H missense 0.00000842
35. 225422453 c.187A>G p.T63A missense 0.00000837
36. 225422448 c.192G>A p.M64I missense 0.00000837
37. 225422536 c.104A>G p.D35G missense 0.00000836
38. 225422504 c.136C>T p.R46C missense 0.00000836
39. 225422522 c.118G>T p.A40S missense 0.00000835
40. 225422519 c.121A>G p.I41V missense 0.00000835
41. 225376269 c.685A>T p.S229C missense 0.00000831
42. 225360565 c.1826A>G p.E609G missense 0.00000830
43. 225346787 c.1851G>T p.Q617H missense 0.00000829
44. 225376266 c.688G>A p.A230T missense 0.00000829
45. 225339074 c.2195C>T p.A732V missense 0.00000829
46. 225370809 c.1070T>G p.L357R missense 0.00000828
47. 225378275 c.620C>T p.A207V missense 0.00000827
48. 225371679 c.925G>T p.G309C missense 0.00000826
49. 225376076 c.878C>T p.T293I missense 0.00000826
50. 225360583 c.1808T>C p.M603T missense 0.00000826
51. 225346771 c.1867C>A p.P623T missense 0.00000826
52. 225370785 c.1094T>G p.L365R missense 0.00000826
53. 225370789 c.1090C>T p.R364C missense 0.00000826
54. 225346773 c.1865T>C p.I622T missense 0.00000826
55. 225362559 c.1618T>G p.L540V missense 0.00000825
56. 225376247 c.707A>G p.K236R missense 0.00000825
57. 225370764 c.1115G>A p.G372D missense 0.00000825
58. 225379339 c.529G>T p.V177F missense 0.00000825
59. 225339039 c.2230C>T p.R744C missense 0.00000825
60. 225371627 c.977A>G p.K326R missense 0.00000825
61. 225371645 c.959A>G p.Y320C missense 0.00000825
62. 225379384 c.484C>T p.R162W missense 0.00000824
63. 225346671 c.1967G>A p.G656D missense 0.00000824
64. 225338988 c.2281C>T p.R761C missense 0.00000824
65. 225362492 c.1685C>T p.T562I missense 0.00000824
66. 225342921 c.2171C>T p.A724V missense 0.00000824
67. 225338984 c.2285A>G p.K762R missense 0.00000824
68. 225365111 c.1579G>C p.A527P missense 0.00000824
69. 225346672 c.1966G>T p.G656C missense 0.00000824
70. 225379396 c.472A>G p.R158G missense 0.00000824
71. 225376155 c.799G>C p.E267Q missense 0.00000824
72. 225362517 c.1660A>G p.M554V missense 0.00000824
73. 225342975 c.2117C>G p.A706G missense 0.00000824
74. 225376097 c.857A>G p.H286R missense 0.00000824
75. 225338987 c.2282G>T p.R761L missense 0.00000824
76. 225365102 c.1588C>T p.H530Y missense 0.00000824
77. 225367704 c.1463G>A p.R488K missense 0.00000824
78. 225365188 c.1502T>G p.V501G missense 0.00000824
79. 225379383 c.485G>C p.R162P missense 0.00000824
80. 225376193 c.761A>C p.K254T missense 0.00000824
81. 225376175 c.779T>C p.I260T missense 0.00000824
82. 225343000 c.2092G>A p.D698N missense 0.00000824
83. 225367749 c.1418T>C p.M473T missense 0.00000824
84. 225362540 c.1637G>A p.R546Q missense 0.00000824
85. 225376133 c.821A>G p.K274R missense 0.00000824
86. 225338987 c.2282G>A p.R761H missense 0.00000824
87. 225376176 c.778A>G p.I260V missense 0.00000824
88. 225376220 c.734T>C p.I245T missense 0.00000824
89. 225342936 c.2156A>G p.H719R missense 0.00000824
90. 225367767 c.1400C>T p.T467M 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.