FHL1 splice variants in ExAC


The table below lists the FHL1 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. 0 c.689-12_689-8delTTTTC splice site 0.00001177
2. 0 c.689-13T>C splice site 0.01062853
3. 0 c.689-13_689-8delTTTTTCinsTTTTCTTTTC splice site 0.00001177
4. 135288561 c.-26-5C>T splice site 0.00177946
5. 135288752 c.156+5C>T splice site 0.00188129
6. 135288753 c.156+6G>A splice site 0.00002280
7. 135289353 c.331+4C>T splice site 0.00001209
8. 135289943 c.332-8C>T splice site 0.00001160
9. 135289944 c.332-7T>C splice site 0.00001158
10. 135290125 c.501+5G>A splice site 0.00001148
11. 135290127 c.501+7T>G splice site 0.00001148
12. 135290804 c.688+4G>T splice site 0.00001140
13. 135290807 c.688+7T>C splice site 0.00001140
14. 135290808 c.688+8A>G splice site 0.00002281
15. 135292019 c.689-11_689-8delTTTC splice site 0.00004754
16. 135292021 c.689-9T>C splice site 0.00012610
17. 135292022 c.689-8C>T splice site 0.49447772
18. 135292022 c.689-8delC splice site 0.00590171
19. 135292022 c.689-8_689-7insC splice site 0.00002522
20. 135292025 c.689-5C>A splice site 0.00005747
21. 135292027 c.689-3_689-2insA splice site 0.00001148
22. 135292031 c.690G>A splice site 0.00001145

* 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.