FHL1 missense variants in ExAC

FHL1 gene summary
FHL1 variants in

The table below lists the FHL1 missense 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 frequency▼Populations*
1. 135289301 c.283C>T p.R95W missense 0.00052359●●●●●●
2. 135288596 c.5C>T p.A2V missense 0.00002279●●●●●●
3. 135289223 c.205G>A p.A69T missense 0.00001144●●●●●●
4. 135289980 c.361G>A p.V121I missense 0.00007997●●●●●●
5. 135290028 c.409G>A p.G137R missense 0.00001141●●●●●●
6. 135292110 c.769G>A p.V257M missense 0.00002279●●●●●●
7. 135292164 c.823G>A p.D275N missense 0.01128128●●●●●●
8. 135288737 c.146C>T p.A49V missense 0.00002280●●●●●●
9. 135289962 c.343G>T p.V115L missense 0.00002292●●●●●●
10. 135289248 c.230A>G p.N77S missense 0.00003434●●●●●●
11. 135289290 c.272A>G p.K91R missense 0.00001154●●●●●●
12. 135290668 c.556T>C p.F186L missense 0.00001139●●●●●●
13. 135292102 c.761A>G p.K254R missense 0.00011394●●●●●●
14. 135288609 c.18C>G p.D6E missense 0.00001140●●●●●●
15. 135288661 c.70G>A p.G24S missense 0.00001139●●●●●●
16. 135288712 c.121G>A p.V41M missense 0.00001140●●●●●●
17. 135288727 c.136C>T p.P46S missense 0.00001140●●●●●●
18. 135289185 c.167A>G p.Y56C missense 0.00001147●●●●●●
19. 135289209 c.191C>T p.T64I missense 0.00001144●●●●●●
20. 135289218 c.200G>A p.R67H missense 0.00001144●●●●●●
21. 135289272 c.254A>G p.N85S missense 0.00001147●●●●●●
22. 135289310 c.292T>A p.S98T missense 0.00003508●●●●●●
23. 135289311 c.293C>A p.S98Y missense 0.00001171●●●●●●
24. 135289317 c.299A>C p.K100T missense 0.00001174●●●●●●
25. 135289325 c.307G>T p.G103W missense 0.00001180●●●●●●
26. 135289335 c.317A>G p.K106R missense 0.00001188●●●●●●
27. 135289337 c.319G>A p.A107T missense 0.00001190●●●●●●
28. 135289341 c.323T>C p.I108T missense 0.00001195●●●●●●
29. 135289962 c.343G>A p.V115M missense 0.00004585●●●●●●
30. 135289971 c.352A>G p.K118E missense 0.00004576●●●●●●
31. 135289974 c.355G>T p.G119W missense 0.00001143●●●●●●
32. 135290019 c.400C>G p.Q134E missense 0.00001141●●●●●●
33. 135290035 c.416G>A p.G139E missense 0.00001141●●●●●●
34. 135290037 c.418A>C p.S140R missense 0.00001141●●●●●●
35. 135290086 c.467C>T p.T156I missense 0.00001142●●●●●●
36. 135290086 c.467C>A p.T156N missense 0.00001142●●●●●●
37. 135290119 c.500A>G p.K167R missense 0.00001146●●●●●●
38. 135290615 c.503C>T p.A168V missense 0.00001140●●●●●●
39. 135290716 c.604G>A p.A202T missense 0.00034182●●●●●●
40. 135290768 c.656A>T p.K219M missense 0.00002279●●●●●●
41. 135290773 c.661T>C p.C221R missense 0.00001140●●●●●●
42. 135290792 c.680C>A p.P227H missense 0.00002280●●●●●●
43. 135292080 c.739G>A p.D247N missense 0.00002279●●●●●●
44. 135292110 c.769G>C p.V257L missense 0.00002279●●●●●●
45. 135292119 c.778G>A p.A260T missense 0.00001139●●●●●●
46. 135292125 c.784A>G p.K262E missense 0.00002279●●●●●●
47. 135292149 c.808C>G p.Q270E missense 0.00002279●●●●●●
48. 135292152 c.811G>C p.V271L missense 0.00001139●●●●●●
49. 135292153 c.812T>C p.V271A missense 0.00001139●●●●●●
50. 135292156 c.815A>T p.Y272F missense 0.00003418●●●●●●

* 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.