JAG1 splice variants in ExAC


The table below lists the JAG1 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. 10629766 c.1349-11T>G splice site 0.00142652
2. 10644666 c.388-4G>C splice site 0.00093920
3. 10644601 c.439+10G>A splice site 0.00037072
4. 10632219 c.1120+10A>G splice site 0.00036073
5. 10621899 c.2917-7G>A splice site 0.00010757
6. 10629762 c.1349-7T>A splice site 0.00006930
7. 10630167 c.1348+3G>A splice site 0.00005155
8. 10625997 c.2113+7G>A splice site 0.00004942
9. 10626740 c.1886-8T>G splice site 0.00004127
10. 10626731 c.1887T>C splice site 0.00004122
11. 10644673 c.388-11_388-8delTTGT splice site 0.00004119
12. 10629764 c.1349-9_1349-6delATTT splice site 0.00003456
13. 10629758 c.1349-3dupT splice site 0.00003437
14. 10623130 c.2572+6T>C splice site 0.00001686
15. 10628603 c.1720+5C>T splice site 0.00001654
16. 10639113 c.694+3A>G splice site 0.00001653
17. 10644666 c.388-4G>T splice site 0.00001648
18. 10625504 c.2344+7G>A splice site 0.00001648
19. 10625786 c.2227+5C>G splice site 0.00001647
20. 10632350 c.1007-8T>G splice site 0.00001008
21. 10631014 c.1121-6G>A splice site 0.00000995
22. 10620609 c.3200-6T>G splice site 0.00000925
23. 10624518 c.2373-7T>A splice site 0.00000876
24. 10653349 c.387G>A splice site 0.00000864
25. 10632230 c.1119A>C splice site 0.00000858
26. 10625031 c.2346T>C splice site 0.00000851
27. 10624998 c.2372+7G>C splice site 0.00000844
28. 10623132 c.2572+4T>C splice site 0.00000841
29. 10629378 c.1396-8T>C splice site 0.00000831
30. 10629379 c.1396-9_1396-7delCTC splice site 0.00000830
31. 10621899 c.2917-7G>C splice site 0.00000827
32. 10626741 c.1886-9G>A splice site 0.00000827
33. 10629702 c.1395+7A>G splice site 0.00000827
34. 10639110 c.694+6T>C splice site 0.00000826
35. 10622550 c.2573-10C>T splice site 0.00000825
36. 10626736 c.1886-4A>G splice site 0.00000825
37. 10626735 c.1886-3T>C splice site 0.00000825
38. 10633109 c.886+7C>A splice site 0.00000825
39. 10626121 c.2000-4C>G splice site 0.00000825
40. 10625911 c.2114-7C>T splice site 0.00000824
41. 10625633 c.2228-6T>C splice site 0.00000824
42. 10632772 c.1006+7G>T splice site 0.00000824
43. 10622423 c.2682+8A>G splice site 0.00000824
44. 10621426 c.3199+5G>T splice site 0.00000824
45. 10622424 c.2682+7C>G splice site 0.00000824
46. 10621757 c.3048+4A>C splice site 0.00000824
47. 10644671 c.388-9G>A splice site 0.00000824
48. 10644673 c.388-11_388-8delTTGTinsTTG splice site 0.00000824
49. 10628756 c.1572G>A 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.