HSP90AA1 splice variants in ExAC


The table below lists the HSP90AA1 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. 102549873 c.1486+10C>T splice site 0.06538036
2. 102548441 c.2089+7C>A splice site 0.00389289
3. 102550121 c.1338+9A>G splice site 0.00155888
4. 102550733 c.1147+3A>G splice site 0.00128643
5. 102551777 c.530-9C>T splice site 0.00016195
6. 102551777 c.530-9C>G splice site 0.00014491
7. 102551778 c.530-10_530-8delTCT splice site 0.00008469
8. 102549644 c.1487-5C>A splice site 0.00007417
9. 102550038 c.1339-8T>C splice site 0.00004951
10. 102550038 c.1339-8dupT splice site 0.00004950
11. 102551777 c.530-9_530-7delCTC splice site 0.00003371
12. 102548441 c.2089+7C>G splice site 0.00001849
13. 102551775 c.530-7C>T splice site 0.00001694
14. 102551344 c.664-9_664-7delCTT splice site 0.00001674
15. 102551333 c.666G>A splice site 0.00001673
16. 102550127 c.1338+3T>C splice site 0.00001666
17. 102551628 c.663+7T>G splice site 0.00001661
18. 102551632 c.663+3A>G splice site 0.00001661
19. 102552543 c.162+11T>C splice site 0.00001657
20. 102552547 c.162+7C>T splice site 0.00001656
21. 102549879 c.1486+4dupA splice site 0.00001651
22. 0 c.1-4C>T splice site 0.00001650
23. 102550038 c.1339-8T>G splice site 0.00001650
24. 102551015 c.981+3G>C splice site 0.00001648
25. 102548786 c.1756-5delT splice site 0.00000881
26. 102550327 c.1148-7T>C splice site 0.00000875
27. 102550319 c.1149C>T p.N383N splice site 0.00000860
28. 102551774 c.530-6T>C splice site 0.00000843
29. 102551338 c.664-3A>G splice site 0.00000837
30. 102551341 c.664-6T>G splice site 0.00000837
31. 102550126 c.1338+4G>C splice site 0.00000833
32. 102552089 c.529+6C>T splice site 0.00000828
33. 102552551 c.162+3A>G splice site 0.00000828
34. 102550908 c.982-7A>G splice site 0.00000827
35. 102550909 c.982-8T>C splice site 0.00000827
36. 0 c.1-8C>G splice site 0.00000825
37. 102549880 c.1486+3A>G splice site 0.00000825
38. 102552722 c.1-7G>C splice site 0.00000825
39. 102549638 c.1488T>C splice site 0.00000824
40. 102549645 c.1487-6_1487-5insA splice site 0.00000824
41. 102549367 c.1755+4T>C splice site 0.00000824
42. 102551010 c.981+8A>G splice site 0.00000824
43. 102549365 c.1755+6T>G splice site 0.00000824
44. 102548166 c.2090-8G>A splice site 0.00000824
45. 102548161 c.2090-3C>T splice site 0.00000824
46. 102549644 c.1487-5C>T splice site 0.00000824
47. 102549366 c.1755+5G>C splice site 0.00000824
48. 102549645 c.1487-6C>T 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.