ANKRD1 truncating variants in ExAC


The table below lists the ANKRD1 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 frequencyPopulations*
1. 92679011 c.222dupA p.Leu75ThrfsTer8 frameshift 0.00009957
2. 92672650 c.933C>A p.Y311X nonsense 0.00002471
3. 92678887 c.345+1G>T essential splice site 0.00001651
4. 92675537 c.750+2T>C essential splice site 0.00001649
5. 92679978 c.155delC p.Pro52LeufsTer2 frameshift 0.00001647
6. 92679953 c.180G>A p.W60X nonsense 0.00001647
7. 92678988 c.245_249delAAAAT p.Glu82ValfsTer5 frameshift 0.00000880
8. 92676032 c.553-6_553-1dupGTATAG nonsense 0.00000829
9. 92676010 c.569delT p.Ile190ThrfsTer13 frameshift 0.00000827
10. 92678896 c.337G>T p.E113X nonsense 0.00000826
11. 92680757 c.27+1G>T essential splice site 0.00000826
12. 92679937 c.196C>T p.R66X nonsense 0.00000824
13. 92675539 c.750_750+1delAG essential splice site 0.00000824
14. 92675538 c.750+1G>C essential splice site 0.00000824
15. 92672720 c.863delC p.Pro288ArgfsTer29 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.