Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.120 | 10 | 5049762 | intron variant | C/T | snv | 0.30 |
|
0.710 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
10 | 5095844 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||||
|
10 | 5095844 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||||
|
10 | 5045786 | intron variant | G/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.030 | 1.000 | 3 | 2013 | 2019 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.030 | 1.000 | 3 | 2013 | 2019 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.020 | 1.000 | 2 | 2011 | 2016 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.020 | 1.000 | 2 | 2011 | 2016 | |||||||
|
1.000 | 0.040 | 10 | 5098945 | intron variant | A/G | snv | 0.19 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.010 | < 0.001 | 1 | 2015 | 2015 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.776 | 0.280 | 10 | 5094459 | missense variant | C/G | snv | 0.50 | 0.45 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.120 | 10 | 5093956 | intron variant | A/G | snv | 0.45 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.120 | 10 | 5094307 | intron variant | A/G | snv | 0.35 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.925 | 0.120 | 10 | 5049762 | intron variant | C/T | snv | 0.30 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.120 | 10 | 5102173 | missense variant | G/A | snv |
|
0.010 | 1.000 | 1 | 2015 | 2015 |