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 | 0.040 | 11 | 113416935 | missense variant | C/T | snv | 4.4E-05 | 6.3E-05 |
|
0.010 | 1.000 | 1 | 2000 | 2000 | |||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.040 | 1.000 | 4 | 2012 | 2017 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2007 | 2014 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2011 | 2014 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 0.500 | 2 | 2015 | 2019 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2016 | 2018 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 0.500 | 2 | 2015 | 2019 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.925 | 0.120 | 11 | 113425286 | intron variant | A/G | snv | 0.65 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 11 | 113425286 | intron variant | A/G | snv | 0.65 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
11 | 113425897 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 |
|
0.020 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 |
|
0.020 | 1.000 | 2 | 2014 | 2017 | ||||||||
|
0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 11 | 113418460 | intron variant | T/C | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2013 | 2014 | ||||||||
|
1.000 | 0.040 | 11 | 113413797 | intron variant | T/G | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
1.000 | 0.040 | 11 | 113413797 | intron variant | T/G | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
1.000 | 0.040 | 11 | 113413797 | intron variant | T/G | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
1.000 | 0.040 | 11 | 113412643 | missense variant | T/A;C | snv | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2013 | 2013 |