TPM1 splice variants in ExAC


The table below lists the TPM1 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. 63351759 c.375-3C>T splice site 0.00181288
2. 63336222 c.115-4C>T splice site 0.00000910
3. 63351757 c.375-5T>C splice site 0.00027194
4. 63353145 c.563+7G>A splice site 0.00004156
5. 63356257 c.773-6T>A splice site 0.00000840
6. 63356347 c.851+6C>T splice site 0.00026633
7. 63358088 c.852-7C>G splice site 0.00003138
8. 63358091 c.852-4G>A splice site 0.00004183
9. 63353901 c.564-11G>A splice site 0.00052790
10. 63353907 c.564-5A>G splice site 0.00002474
11. 63353908 c.564-4T>A splice site 0.00000825
12. 0 c.639+12delG splice site 0.00032765
13. 63335146 c.114+4T>C splice site 0.00002001
14. 63335149 c.114+7G>A splice site 0.00002223
15. 63336221 c.115-5C>G splice site 0.00000914
16. 63336223 c.115-3C>T splice site 0.00000906
17. 63349176 c.241-8C>T splice site 0.00000824
18. 63349324 c.374+7A>G splice site 0.00001648
19. 63351887 c.492+8C>T splice site 0.00000826
20. 63353061 c.493-7G>A splice site 0.00001648
21. 63353144 c.563+6C>T splice site 0.00000831
22. 63353144 c.563+6C>A splice site 0.00000831
23. 63353991 c.639+4G>A splice site 0.00000833
24. 63354483 c.702+7T>A splice site 0.00000825
25. 63356258 c.773-5C>T splice site 0.00000840
26. 63356264 c.774C>T splice site 0.00005879
27. 63356344 c.851+3A>G splice site 0.00000935
28. 63356347 c.851+6C>A splice site 0.00004756
29. 63356348 c.851+7G>A splice site 0.00002858
30. 63358095 c.852A>T splice site 0.00001042

* 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.