ABCC9 truncating variants in ExAC

ABCC9 gene summary
ABCC9 variants in DCM

The table below lists the ABCC9 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. 22063090 c.1320+1G>A essential splice site 0.00005814●●●●●●
2. 22048252 c.1619-3_1619-2delCA essential splice site 0.00002494●●●●●●
3. 22086715 c.284+1G>A essential splice site 0.00002475●●●●●●
4. 22005391 c.2554C>T p.Q852X nonsense 0.00002474●●●●●●
5. 22012582 c.2443G>T p.G815X nonsense 0.00001648●●●●●●
6. 22089465 c.142+2T>C essential splice site 0.00000902●●●●●●
7. 22059149 c.1529G>A p.W510X nonsense 0.00000836●●●●●●
8. 21962890 c.4212-1G>T essential splice site 0.00000835●●●●●●
9. 22048210 c.1658dupC p.Thr554TyrfsTer54 frameshift 0.00000832●●●●●●
10. 22069869 c.573+2T>G essential splice site 0.00000832●●●●●●
11. 21970242 c.3772-1G>A essential splice site 0.00000830●●●●●●
12. 22089608 c.1delA p.Met1? frameshift 0.00000830●●●●●●
13. 22017371 c.2237+2T>C essential splice site 0.00000830●●●●●●
14. 22005157 c.2644-1G>C essential splice site 0.00000829●●●●●●
15. 22040843 c.1828_1829delTT p.Leu610GlufsTer2 frameshift 0.00000829●●●●●●
16. 22005094 c.2706delA p.Asp903MetfsTer12 frameshift 0.00000829●●●●●●
17. 22005032 c.2768delA p.Lys923ArgfsTer10 frameshift 0.00000828●●●●●●
18. 21970119 c.3892+2T>C essential splice site 0.00000827●●●●●●
19. 21958187 c.4571_4572dupTA p.Val1525Ter frameshift 0.00000826●●●●●●
20. 22063138 c.1273_1274delAT p.Met425ValfsTer8 frameshift 0.00000825●●●●●●
21. 21998616 c.3017delC p.Ser1006TrpfsTer4 frameshift 0.00000825●●●●●●
22. 22065869 c.948_949delTT p.Cys317TyrfsTer10 frameshift 0.00000825●●●●●●
23. 22063805 c.1119C>G p.Y373X nonsense 0.00000825●●●●●●
24. 21971182 c.3673_3674insT p.Tyr1225LeufsTer16 frameshift 0.00000825●●●●●●
25. 22025653 c.2104delA p.Met702Ter frameshift 0.00000824●●●●●●
26. 22086828 c.172dupA p.Ile58AsnfsTer13 frameshift 0.00000824●●●●●●
27. 22012601 c.2425-1G>T essential splice site 0.00000824●●●●●●
28. 21960374 c.4355_4356delGA p.Gly1452AlafsTer22 frameshift 0.00000824●●●●●●
29. 21971082 c.3771+2T>G essential splice site 0.00000824●●●●●●
30. 21981908 c.3653G>A p.W1218X nonsense 0.00000824●●●●●●
31. 22086831 c.169C>T p.Q57X nonsense 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.