TNNC1 protein-altering variants in ExAC

TNNC1 gene summary
TNNC1 variants in DCM, HCM

The table below lists the TNNC1 protein-altering 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. 52485419 c.442A>G p.I148V missense 0.00000829●●●●●●
2. 52485428 c.433G>A p.D145N missense 0.00000829●●●●●●
3. 52485772 c.305G>T p.R102L missense 0.00001651●●●●●●
4. 52485505 c.356T>C p.I119T missense 0.00000828●●●●●●
5. 52485772 c.305G>A p.R102H missense 0.00000826●●●●●●
6. 52485501 c.360G>A p.M120I missense 0.00000828●●●●●●
7. 52485524 c.337G>A p.D113N missense 0.00001655●●●●●●
8. 52485773 c.304C>T p.R102C missense 0.00000825●●●●●●
9. 52485834 c.243G>C p.M81I missense 0.00000825●●●●●●
10. 52485303 c.474G>C p.K158N missense 0.00000830●●●●●●
11. 52485308 c.469A>C p.M157L missense 0.00000829●●●●●●
12. 52485421 c.440G>A p.R147H missense 0.00000830●●●●●●
13. 52485425 c.436G>A p.G146S missense 0.00001659●●●●●●
14. 52485426 c.435C>G p.D145E missense 0.00000829●●●●●●
15. 52485430 c.431A>G p.N144S missense 0.00000829●●●●●●
16. 52485435 c.426G>C p.K142N missense 0.00000829●●●●●●
17. 52485442 c.419G>A p.G140E missense 0.00000829●●●●●●
18. 52485451 c.410T>C p.M137T missense 0.00000829●●●●●●
19. 52485458 c.403G>A p.E135K missense 0.00000829●●●●●●
20. 52485475 c.386C>T p.T129M missense 0.00000829●●●●●●
21. 52485485 c.376G>A p.E126K missense 0.00000828●●●●●●
22. 52485494 c.367G>A p.A123T missense 0.00000828●●●●●●
23. 52485527 c.334A>T p.I112F missense 0.00000828●●●●●●
24. 52485761 c.316A>C p.K106Q missense 0.00000826●●●●●●
25. 52485779 c.298C>A p.L100I missense 0.00000825●●●●●●
26. 52485818 c.259G>T p.D87Y missense 0.00000825●●●●●●
27. 52485835 c.242T>C p.M81T missense 0.00000825●●●●●●
28. 52485852 c.225T>G p.D75E missense 0.00000825●●●●●●
29. 52485869 c.208G>A p.G70S missense 0.00001651●●●●●●
30. 52488007 c.24+1G>A essential splice site 0.00002368●●●●●●
31. 52486162 c.162delT p.Glu55ArgfsTer6 frameshift 0.00000826●●●●●●

* 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.