| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.742 | 0.320 | 12 | 25245348 | missense variant | C/A;G;T | snv |
|
0.710 | 1.000 | 4 | 2002 | 2013 | |||||||||
|
0.807 | 0.320 | 15 | 66435145 | missense variant | G/A | snv |
|
0.710 | 1.000 | 3 | 2007 | 2016 | |||||||||
|
0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv |
|
0.710 | 1.000 | 2 | 2002 | 2015 | |||||||||
|
0.763 | 0.160 | 10 | 112738717 | intron variant | G/A | snv | 0.20 |
|
0.710 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
1.000 | 0.080 | 4 | 113625548 | intron variant | A/G | snv | 0.18 |
|
0.710 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.080 | 7 | 118351841 | intron variant | A/G | snv | 0.27 |
|
0.710 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv |
|
0.700 | 1.000 | 12 | 2004 | 2014 | |||||||||
|
0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 |
|
0.700 | 1.000 | 11 | 2004 | 2012 | ||||||||
|
0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 |
|
0.700 | 1.000 | 11 | 2004 | 2012 | ||||||||
|
0.583 | 0.600 | 1 | 114713908 | missense variant | T/A;C;G | snv |
|
0.700 | 1.000 | 9 | 1984 | 2014 | |||||||||
|
0.925 | 0.160 | 11 | 533881 | missense variant | C/T | snv |
|
0.700 | 1.000 | 9 | 1982 | 2011 | |||||||||
|
0.689 | 0.400 | 10 | 87957915 | stop gained | C/A;T | snv |
|
0.700 | 1.000 | 7 | 1998 | 2010 | |||||||||
|
0.763 | 0.360 | 7 | 140753355 | missense variant | C/G;T | snv |
|
0.700 | 1.000 | 7 | 2002 | 2010 | |||||||||
|
0.882 | 0.080 | 7 | 140753338 | inframe insertion | -/TAG | delins | 4.0E-06 |
|
0.700 | 1.000 | 6 | 2009 | 2012 | ||||||||
|
0.882 | 0.160 | 7 | 55174818 | missense variant | G/A;T | snv |
|
0.700 | 1.000 | 5 | 2006 | 2014 | |||||||||
|
1.000 | 0.080 | 17 | 39724748 | inframe insertion | -/GGGCTCCCC | delins |
|
0.700 | 1.000 | 5 | 2005 | 2012 | |||||||||
|
0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv |
|
0.700 | 1.000 | 4 | 2002 | 2008 | |||||||||
|
0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv |
|
0.700 | 1.000 | 4 | 2002 | 2013 | |||||||||
|
0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 |
|
0.700 | 1.000 | 4 | 2004 | 2012 | ||||||||
|
0.882 | 0.280 | 12 | 25227345 | missense variant | C/A | snv | 4.0E-06 |
|
0.700 | 1.000 | 4 | 2006 | 2013 | ||||||||
|
0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv |
|
0.700 | 1.000 | 3 | 2002 | 2008 | |||||||||
|
0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 |
|
0.700 | 1.000 | 3 | 2002 | 2013 | ||||||||
|
0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv |
|
0.700 | 1.000 | 3 | 2002 | 2009 | |||||||||
|
0.667 | 0.400 | 1 | 114713907 | missense variant | T/A;G | snv |
|
0.700 | 1.000 | 3 | 2002 | 2013 | |||||||||
|
0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv |
|
0.700 | 1.000 | 3 | 2002 | 2010 |