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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.763 | 0.200 | 17 | 64356203 | missense variant | C/A;T | snv | 0.38 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.763 | 0.200 | 17 | 64356203 | missense variant | C/A;T | snv | 0.38 |
|
0.010 | 1.000 | 1 | 2003 | 2003 | ||||||||
|
1.000 | 0.120 | 17 | 64370017 | missense variant | A/G | snv | 1.4E-05 |
|
0.010 | < 0.001 | 1 | 2002 | 2002 | ||||||||
|
1.000 | 0.040 | 17 | 64390632 | missense variant | A/T | snv | 1.4E-05 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2005 | 2005 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2001 | 2001 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2005 | 2005 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | < 0.001 | 1 | 2002 | 2002 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2003 | 2003 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2003 | 2003 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2004 | 2004 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
1.000 | 0.040 | 17 | 64378896 | intron variant | G/A | snv | 0.40 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.040 | 17 | 64378896 | intron variant | G/A | snv | 0.40 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.040 | 17 | 64330939 | intron variant | A/G | snv | 0.55 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.240 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.851 | 0.240 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.851 | 0.240 | 17 | 64377836 | missense variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 |