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

* 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.