PTBP1 splice variants in ExAC


The table below lists the PTBP1 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. 806559 c.1119+3A>G splice site 0.00767404
2. 808351 c.1154-9C>T splice site 0.00100515
3. 806556 c.1119G>A p.E373E splice site 0.00083045
4. 804442 c.435+4C>T splice site 0.00077817
5. 804825 c.607-4G>A splice site 0.00021494
6. 808361 c.1155C>T p.G385G splice site 0.00013415
7. 808547 c.1248C>T splice site 0.00007821
8. 803644 c.115+8C>T splice site 0.00004954
9. 804219 c.288+11C>T splice site 0.00004215
10. 805186 c.891C>T p.F297F splice site 0.00004162
11. 805191 c.892+4A>C splice site 0.00003336
12. 804947 c.717+8G>C splice site 0.00003327
13. 808542 c.1247-4C>T splice site 0.00002844
14. 804438 c.435G>A splice site 0.00002561
15. 805580 c.970+11G>A splice site 0.00002490
16. 805575 c.970+6C>G splice site 0.00002489
17. 805008 c.718-5C>T splice site 0.00002482
18. 806400 c.971-8delT splice site 0.00002248
19. 808463 c.1246+11G>A splice site 0.00001798
20. 797508 c.8+3G>A splice site 0.00001679
21. 805008 c.718-5C>G splice site 0.00001655
22. 799449 c.39+6C>T splice site 0.00001655
23. 805015 c.720G>A splice site 0.00001654
24. 808451 c.1245G>A splice site 0.00001511
25. 806561 c.1119+5G>T splice site 0.00001136
26. 806561 c.1119+5G>A splice site 0.00001136
27. 808768 c.1463+6T>G splice site 0.00001117
28. 806404 c.971-4C>T splice site 0.00001102
29. 804527 c.436-5C>T splice site 0.00000971
30. 804528 c.436-4A>C splice site 0.00000969
31. 804444 c.435+6T>G splice site 0.00000864
32. 810536 c.1464-7C>A splice site 0.00000846
33. 810537 c.1464-6C>T splice site 0.00000845
34. 810543 c.1464G>A p.P488P splice site 0.00000839
35. 804709 c.606+7T>C splice site 0.00000835
36. 804707 c.606+5G>A splice site 0.00000834
37. 810687 c.1542-7C>T splice site 0.00000830
38. 804033 c.116-3C>T splice site 0.00000828
39. 799451 c.39+8C>T splice site 0.00000827
40. 799406 c.9-7T>A splice site 0.00000827
41. 799409 c.9-4A>G splice site 0.00000827
42. 799402 c.9-11_9-8delTCTC splice site 0.00000827
43. 799410 c.9-3C>G splice site 0.00000827
44. 805006 c.718-7C>A splice site 0.00000827
45. 805010 c.718-3C>T splice site 0.00000827
46. 803643 c.115+7C>T splice site 0.00000826
47. 803554 c.40-7C>T splice site 0.00000826
48. 803642 c.115+6G>T splice site 0.00000826
49. 803640 c.115+4A>T splice site 0.00000825
50. 807906 c.1153+4T>C splice site 0.00000824
51. 807861 c.1120-8C>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.