ANKRD1 truncating variants in ExAC

ANKRD1 gene summary
ANKRD1 variants in DCM

The table below lists the ANKRD1 truncating variants found in the ExAC population database with a mean allelic frequency (MAF) less than 0.0001, classified for this study as a rare variant. 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. 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. 92675538 c.750+1G>C essential splice site 0.00000824●●●●●●
13. 92672720 c.863delC p.Pro288ArgfsTer29 frameshift 0.00000824●●●●●●
14. 92679937 c.196C>T p.R66X nonsense 0.00000824●●●●●●
15. 92675539 c.750_750+1delAG essential splice site 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.