TCAP non-truncating variants in ExAC

TCAP gene summary
TCAP variants in DCM

The table below lists the TCAP non-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. 37821709 c.97C>T p.R33W missense 0.00006646●●●●●●
2. 37822246 c.388C>T p.R130C missense 0.00005866●●●●●●
3. 37822069 c.211A>G p.M71V missense 0.00005192●●●●●●
4. 37822084 c.226C>T p.R76C missense 0.00005169●●●●●●
5. 37822175 c.317G>A p.R106H missense 0.00004315●●●●●●
6. 37822318 c.460C>T p.R154C missense 0.00004192●●●●●●
7. 37822306 c.448G>A p.G150S missense 0.00004170●●●●●●
8. 37821665 c.53G>A p.R18Q missense 0.00004141●●●●●●
9. 37822268 c.410C>A p.T137K missense 0.00003340●●●●●●
10. 37822279 c.421C>G p.P141A missense 0.00003339●●●●●●
11. 37822310 c.452C>T p.A151V missense 0.00003337●●●●●●
12. 37822029 c.171C>G p.C57W missense 0.00003123●●●●●●
13. 37822117 c.259C>T p.R87W missense 0.00002999●●●●●●
14. 37822319 c.461G>A p.R154H missense 0.00002516●●●●●●
15. 37821655 c.43T>A p.C15S missense 0.00002484●●●●●●
16. 37822046 c.188G>A p.R63H missense 0.00002108●●●●●●
17. 37822066 c.208C>T p.R70W missense 0.00002101●●●●●●
18. 37822045 c.187C>T p.R63C missense 0.00002100●●●●●●
19. 37822067 c.209G>A p.R70Q missense 0.00002091●●●●●●
20. 37822081 c.223G>A p.G75S missense 0.00002075●●●●●●
21. 37822338 c.480G>A p.M160I missense 0.00001685●●●●●●
22. 37822236 c.378G>C p.Q126H missense 0.00001679●●●●●●
23. 37822315 c.457C>T p.R153C missense 0.00001675●●●●●●
24. 37822315 c.457C>A p.R153S missense 0.00001675●●●●●●
25. 37821715 c.103G>A p.E35K missense 0.00001664●●●●●●
26. 37821662 c.50G>C p.R17P missense 0.00001656●●●●●●
27. 37821971 c.113G>A p.C38Y missense 0.00001134●●●●●●
28. 37822056 c.198G>C p.W66C missense 0.00001047●●●●●●
29. 37822060 c.202A>T p.M68L missense 0.00001045●●●●●●
30. 37822001 c.143A>G p.H48R missense 0.00001043●●●●●●
31. 37822028 c.170G>A p.C57Y missense 0.00001041●●●●●●
32. 37822070 c.212T>C p.M71T missense 0.00001039●●●●●●
33. 37822012 c.154C>G p.H52D missense 0.00001038●●●●●●
34. 37822009 c.151T>C p.Y51H missense 0.00001038●●●●●●
35. 37822010 c.152A>T p.Y51F missense 0.00001037●●●●●●
36. 37822085 c.227G>A p.R76H missense 0.00001036●●●●●●
37. 37822098 c.240G>T p.E80D missense 0.00001016●●●●●●
38. 37822120 c.262G>T p.V88L missense 0.00000987●●●●●●
39. 37822148 c.290C>T p.A97V missense 0.00000921●●●●●●
40. 37822153 c.295A>G p.M99V missense 0.00000909●●●●●●
41. 37822159 c.301G>A p.A101T missense 0.00000897●●●●●●
42. 37822174 c.316C>A p.R106S missense 0.00000867●●●●●●
43. 37822183 c.325A>G p.T109A missense 0.00000856●●●●●●
44. 37822355 c.497G>A p.R166K missense 0.00000846●●●●●●
45. 37822331 c.473G>A p.R158H missense 0.00000841●●●●●●
46. 37822235 c.377A>G p.Q126R missense 0.00000840●●●●●●
47. 37822245 c.387C>G p.D129E missense 0.00000839●●●●●●
48. 37822318 c.460_471delCGCTCCCTGTCC p.Arg154_Ser157del inframe 0.00000838●●●●●●
49. 37822252 c.394G>A p.E132K missense 0.00000837●●●●●●
50. 37822294 c.436G>T p.V146F missense 0.00000834●●●●●●
51. 37821697 c.85A>T p.T29S missense 0.00000829●●●●●●
52. 37821617 c.5C>T p.A2V missense 0.00000828●●●●●●
53. 37821662 c.50G>A p.R17H missense 0.00000828●●●●●●
54. 37821644 c.32C>G p.S11W missense 0.00000828●●●●●●
55. 37821628 c.16C>A p.L6M missense 0.00000828●●●●●●

* 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.