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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 19 | 41342230 | missense variant | G/A | snv |
|
0.740 | 1.000 | 4 | 2003 | 2014 | |||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.710 | 1.000 | 4 | 2011 | 2016 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.040 | 0.750 | 4 | 2012 | 2019 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.040 | 1.000 | 4 | 2004 | 2017 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.810 | 1.000 | 4 | 2014 | 2018 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.040 | 0.750 | 4 | 2012 | 2019 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.700 | 1.000 | 3 | 2014 | 2016 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.700 | 1.000 | 3 | 2014 | 2016 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.700 | 1.000 | 3 | 2014 | 2016 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.700 | 1.000 | 3 | 2014 | 2016 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.700 | 1.000 | 3 | 2014 | 2016 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.700 | 1.000 | 3 | 2014 | 2016 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.700 | 1.000 | 3 | 2014 | 2016 | ||||||||
|
0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv |
|
0.030 | 0.333 | 3 | 2004 | 2017 | |||||||||
|
0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv |
|
0.030 | 1.000 | 3 | 2011 | 2019 | |||||||||
|
0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv |
|
0.030 | 1.000 | 3 | 2011 | 2018 | |||||||||
|
0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv |
|
0.030 | 1.000 | 3 | 2011 | 2019 | |||||||||
|
0.882 | 0.040 | 19 | 41323701 | 3 prime UTR variant | G/A | snv | 0.15 |
|
0.030 | 0.667 | 3 | 2011 | 2017 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.020 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.020 | 1.000 | 2 | 2012 | 2019 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.020 | 1.000 | 2 | 2012 | 2019 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.020 | 1.000 | 2 | 2006 | 2019 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.020 | 1.000 | 2 | 2012 | 2012 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.020 | 0.500 | 2 | 2013 | 2014 | ||||||||
|
0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 |
|
0.020 | 1.000 | 2 | 2015 | 2019 |