PLOD3 splice variants in ExAC


The table below lists the PLOD3 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. 100855001 c.1233-4G>A splice site 0.06826800
2. 100853807 c.1500+6C>T splice site 0.01294388
3. 100850053 c.2061+7C>A splice site 0.00053621
4. 100854862 c.1358+10G>A splice site 0.00049387
5. 100850855 c.1935+4C>T splice site 0.00032446
6. 100853612 c.1614C>T p.V538V splice site 0.00030116
7. 100855804 c.1005+7_1005+8insAGGAG splice site 0.00019952
8. 100853806 c.1500+7G>A splice site 0.00018221
9. 100853805 c.1500+8C>T splice site 0.00014081
10. 100850190 c.1936-5C>G splice site 0.00013534
11. 100856381 c.777+7C>T splice site 0.00006847
12. 100851013 c.1789-8G>A splice site 0.00005065
13. 100853364 c.1683+10C>T splice site 0.00003703
14. 100859968 c.201+8_201+9insA splice site 0.00003306
15. 100850056 c.2061+4C>T splice site 0.00002868
16. 100856489 c.680-4C>G splice site 0.00002628
17. 100855659 c.1006-4C>T splice site 0.00002487
18. 100858440 c.616-7C>T splice site 0.00002471
19. 100855528 c.1127+6C>T splice site 0.00001657
20. 100853810 c.1500+3G>T splice site 0.00001656
21. 100859686 c.338+5C>T splice site 0.00001648
22. 100859309 c.503-8C>T splice site 0.00001648
23. 100858439 c.616-6delA splice site 0.00001647
24. 100854868 c.1358+4A>G splice site 0.00001644
25. 100853451 c.1615-9C>G splice site 0.00001589
26. 100855003 c.1233-6C>T splice site 0.00001354
27. 100855119 c.1232+8A>C splice site 0.00001139
28. 100856380 c.777+8C>G splice site 0.00000857
29. 100856115 c.879+8G>A splice site 0.00000853
30. 100856229 c.778-5A>G splice site 0.00000849
31. 100853729 c.1501-4A>G splice site 0.00000834
32. 100850854 c.1935+5G>A splice site 0.00000833
33. 100859189 c.615G>A splice site 0.00000833
34. 100855804 c.1005+7C>G splice site 0.00000831
35. 100855811 c.1005C>T splice site 0.00000831
36. 100855664 c.1006-9C>A splice site 0.00000830
37. 100855662 c.1006-7C>G splice site 0.00000829
38. 100855536 c.1125C>T splice site 0.00000828
39. 100855527 c.1127+7G>A splice site 0.00000828
40. 100853958 c.1359-4C>T splice site 0.00000828
41. 100853957 c.1359-3C>T splice site 0.00000828
42. 100859968 c.201+8G>A splice site 0.00000826
43. 100852127 c.1788+7G>T splice site 0.00000826
44. 100859969 c.201+7A>G splice site 0.00000826
45. 100859833 c.202-6C>T splice site 0.00000824
46. 100858439 c.616-6A>G splice site 0.00000824
47. 100859686 c.338+5C>G splice site 0.00000824
48. 100859832 c.202-5dupC splice site 0.00000824
49. 100859830 c.202-3C>T splice site 0.00000824
50. 100859684 c.338+7G>C splice site 0.00000824
51. 100859836 c.202-9_202-7delTCT splice site 0.00000824
52. 100859685 c.338+6G>C splice site 0.00000824
53. 100859304 c.503-3C>G splice site 0.00000824
54. 100852236 c.1686A>G 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.