PKP2 splice variants in ExAC


The table below lists the PKP2 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. 33049437 c.223+6T>A splice site 0.00001306
2. 33031846 c.336+8A>G splice site 0.00000825
3. 33031483 c.337-6G>A splice site 0.00000874
4. 33030776 c.1034+4A>G splice site 0.00000877
5. 33003918 c.1171-11T>C splice site 0.00288930
6. 33003910 c.1171-3C>T splice site 0.00000828
7. 32996251 c.1379-4A>G splice site 0.00000832
8. 32996246 c.1380C>T splice site 0.00000833
9. 32994144 c.1511-5T>C splice site 0.00001662
10. 32993964 c.1686A>G splice site 0.00000824
11. 32993955 c.1688+7C>T splice site 0.00002472
12. 32993953 c.1688+9A>G splice site 0.00049444
13. 32977104 c.1689-8dupT splice site 0.00388513
14. 32976976 c.1806+3A>G splice site 0.00000825
15. 32974469 c.1972-6G>T splice site 0.00000826
16. 32974468 c.1972-5G>C splice site 0.00002478
17. 32974461 c.1974A>G p.Q658Q splice site 0.00004127
18. 32955330 c.2299+7C>T splice site 0.03238940
19. 32955329 c.2299+8G>A splice site 0.00004945
20. 32955326 c.2299+11A>G splice site 0.00001649
21. 32949238 c.2300-6T>C splice site 0.00017741
22. 32949236 c.2300-4G>C splice site 0.00008079
23. 32949236 c.2300-4G>A splice site 0.00000898
24. 32949045 c.2487T>C p.D829D splice site 0.00009061
25. 32945671 c.2490-6T>C splice site 0.00002472
26. 32945433 c.2578-7T>G splice site 0.00000824
27. 32945431 c.2578-5C>T splice site 0.00000824
28. 32945430 c.2578-4A>C 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.