HFE truncating variants in ExAC

HFE gene summary
HFE variants in

The table below lists the HFE truncating 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. 26093461 c.1006+1G>A essential splice site 0.00006648●●●●●●
2. 26094422 c.1015_1016insG p.Met339SerfsTer8 frameshift 0.00003296●●●●●●
3. 26091747 c.546_547delCC p.Leu183GlyfsTer60 frameshift 0.00002489●●●●●●
4. 26091203 c.211C>T p.R71X nonsense 0.00002471●●●●●●
5. 26091818 c.616+1G>T essential splice site 0.00000853●●●●●●
6. 26087746 c.76+2T>C essential splice site 0.00000845●●●●●●
7. 26091775 c.574C>T p.Q192X nonsense 0.00000834●●●●●●
8. 26091679 c.478delC p.Arg161GlyfsTer50 frameshift 0.00000825●●●●●●
9. 26091269 c.277delG p.Trp94GlyfsTer117 frameshift 0.00000824●●●●●●
10. 26093026 c.730C>T p.Q244X nonsense 0.00000824●●●●●●
11. 26093188 c.892G>T p.E298X nonsense 0.00000824●●●●●●
12. 26093353 c.899C>A p.S300X nonsense 0.00000824●●●●●●
13. 26093088 c.792C>G p.Y264X nonsense 0.00000824●●●●●●
14. 26093186 c.890G>A p.W297X nonsense 0.00000824●●●●●●
15. 26092993 c.697C>T p.Q233X nonsense 0.00000824●●●●●●
16. 26092961 c.665_666delCT p.Leu223ThrfsTer20 frameshift 0.00000824●●●●●●
17. 26093421 c.967delG p.G323Efs*5 frameshift 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.