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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.708 | 0.440 | 13 | 20189473 | missense variant | C/A;T | snv | 7.7E-03 |
|
0.800 | 0.900 | 10 | 2004 | 2017 | ||||||||
|
0.790 | 0.200 | 13 | 20189481 | missense variant | A/C;G | snv | 8.7E-03 |
|
0.740 | 0.833 | 6 | 2001 | 2012 | ||||||||
|
0.752 | 0.280 | 13 | 20189031 | missense variant | C/G;T | snv | 6.0E-05 |
|
0.730 | 0.667 | 3 | 2010 | 2017 | ||||||||
|
0.882 | 0.200 | 13 | 20189359 | missense variant | G/A;C | snv |
|
0.720 | 1.000 | 2 | 2000 | 2001 | |||||||||
|
1.000 | 0.120 | 5 | 146340095 | missense variant | T/C | snv |
|
0.020 | 1.000 | 2 | 2008 | 2009 | |||||||||
|
0.925 | 0.120 | 13 | 20189450 | stop gained | C/G;T | snv | 2.8E-05 |
|
0.710 | 1.000 | 1 | 2001 | 2001 | ||||||||
|
0.925 | 0.160 | 15 | 72347711 | missense variant | T/C;G | snv | 4.0E-06 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.925 | 0.160 | 15 | 72345518 | stop gained | C/T | snv | 4.0E-06 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | X | 71223772 | missense variant | G/A | snv |
|
0.010 | 1.000 | 1 | 2001 | 2001 | |||||||||
|
1.000 | 0.120 | 13 | 20189202 | missense variant | C/A;T | snv | 2.8E-04; 1.4E-02 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.925 | 0.160 | 7 | 107675050 | missense variant | C/G | snv | 4.8E-05 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.851 | 0.200 | 3 | 150972520 | stop gained | G/A;T | snv | 1.2E-05; 1.2E-05 |
|
0.010 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
0.882 | 0.120 | 2 | 178456149 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06; 4.0E-06 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.882 | 0.240 | X | 71223930 | missense variant | C/A;T | snv |
|
0.010 | 1.000 | 1 | 2000 | 2000 | |||||||||
|
3 | 121993482 | missense variant | C/A;T | snv |
|
0.010 | 1.000 | 1 | 2011 | 2011 | |||||||||||
|
0.925 | 0.120 | 6 | 73482214 | missense variant | G/A | snv |
|
0.010 | 1.000 | 1 | 2003 | 2003 | |||||||||
|
1.000 | 0.120 | 3 | 7114015 | intron variant | T/A;G | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.120 | 9 | 72816161 | missense variant | G/A;C | snv |
|
0.010 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.827 | 0.200 | 3 | 150972591 | missense variant | A/C;G | snv | 8.0E-05; 4.0E-06 |
|
0.010 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
0.925 | 0.120 | 14 | 30878897 | missense variant | T/A;C | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.120 | 11 | 77162149 | missense variant | A/G;T | snv | 1.3E-05 |
|
0.010 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
6 | 85493984 | missense variant | A/G | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2002 | 2002 | ||||||||||
|
14 | 76439579 | missense variant | T/C | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
6 | 33177678 | missense variant | C/G | snv | 4.1E-06 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
1.000 | 0.080 | 11 | 2445213 | stop gained | G/T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 |