CCT4 splice variants in ExAC


The table below lists the CCT4 splice 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. 62104048 c.777+7A>G splice site 0.00117280
2. 62100322 c.1014+10dupT splice site 0.00023128
3. 62115508 c.127+8T>C splice site 0.00008169
4. 62107414 c.379+7A>G splice site 0.00007440
5. 62100134 c.1125+3_1125+6dupAACA splice site 0.00007418
6. 62103223 c.917+7G>T splice site 0.00005014
7. 62110587 c.270+7G>A splice site 0.00003998
8. 62112215 c.128-8dupA splice site 0.00003498
9. 62103227 c.917+3G>T splice site 0.00003332
10. 62103219 c.917+11A>G splice site 0.00002515
11. 62103224 c.917+6G>A splice site 0.00001670
12. 62104191 c.645-4T>G splice site 0.00001654
13. 62103375 c.778-6G>A splice site 0.00001654
14. 62100328 c.1014+4A>G splice site 0.00001653
15. 62107527 c.273G>C splice site 0.00001648
16. 62104653 c.523-4C>G splice site 0.00001360
17. 62110688 c.181-5T>G splice site 0.00001137
18. 62110681 c.183T>C splice site 0.00001085
19. 62115509 c.127+7C>T splice site 0.00000907
20. 62112213 c.128-6C>T splice site 0.00000842
21. 62096696 c.1492-8A>T splice site 0.00000838
22. 62096572 c.1605+3A>G splice site 0.00000838
23. 62104055 c.777C>T splice site 0.00000837
24. 62096692 c.1492-4G>T splice site 0.00000837
25. 62104530 c.642T>C splice site 0.00000831
26. 62099587 c.1256+6G>A splice site 0.00000830
27. 62099726 c.1126-3A>T splice site 0.00000827
28. 62103377 c.778-8delC splice site 0.00000827
29. 62095845 c.1606-4T>C splice site 0.00000826
30. 62107422 c.378A>G splice site 0.00000825
31. 62100251 c.1015-4C>T splice site 0.00000824
32. 62107529 c.271C>T splice site 0.00000824
33. 62100254 c.1015-7T>G splice site 0.00000824
34. 62107535 c.271-6A>T splice site 0.00000824
35. 62100251 c.1015-4_1015-3insT splice site 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.