LDB3 truncating variants in ExAC


The table below lists the LDB3 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 frequencyPopulations*
1. 88441526 c.655C>T p.R219X nonsense 0.00003486
2. 88452309 c.877G>T p.E293X nonsense 0.00000824
3. 88469728 c.1152C>A p.Y384X nonsense 0.00000854
4. 88476473 c.1621C>T p.R541X nonsense 0.00000881
5. 88477784 c.1740C>A p.C580X nonsense 0.00000824
6. 88477842 c.1798C>T p.R600X nonsense 0.00004942
7. 88492668 c.2119C>T p.Q707X nonsense 0.00000892
8. 88439915 c.321+1G>A essential splice site 0.00001679
9. 88441561 c.689+1G>A essential splice site 0.00000893
10. 88477720 c.1677-1G>A essential splice site 0.00001655
11. 88451707 c.744_745delTG p.Val249AspfsTer2 frameshift 0.00000824
12. 88451727 c.764_765insGCCAGAACAT p.Asp258HisfsTer5 frameshift 0.00000824
13. 88466336 c.945_972delGCTGCTGCCCGCTTCTGCCCAGCCACCT p.Ala319LeufsTer164 frameshift 0.00000838
14. 88466398 c.1007delT p.Leu336ArgfsTer156 frameshift 0.00002522
15. 88476368 c.1516delA p.Thr506ProfsTer59 frameshift 0.00000827
16. 88478508 c.1882delA p.Thr628HisfsTer75 frameshift 0.00000824
17. 88485941 c.2026delG p.Val676TrpfsTer27 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.