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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.160 | 6 | 137874014 | intron variant | G/T | snv | 0.13 |
|
0.740 | 1.000 | 5 | 2009 | 2017 | ||||||||
|
0.790 | 0.320 | 6 | 32315077 | intron variant | A/G | snv | 0.14 |
|
0.810 | 1.000 | 5 | 2007 | 2016 | ||||||||
|
0.752 | 0.560 | 1 | 157701026 | upstream gene variant | A/G | snv | 0.57 |
|
0.050 | 1.000 | 5 | 2006 | 2016 | ||||||||
|
0.925 | 0.160 | 4 | 26106575 | downstream gene variant | G/C | snv | 0.29 |
|
0.820 | 1.000 | 5 | 2010 | 2016 | ||||||||
|
0.925 | 0.200 | 6 | 32827255 | 3 prime UTR variant | G/A | snv | 6.1E-02 |
|
0.800 | 1.000 | 4 | 2007 | 2016 | ||||||||
|
0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 |
|
0.820 | 1.000 | 4 | 2010 | 2016 | ||||||||
|
0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv |
|
0.040 | 1.000 | 4 | 2005 | 2018 | |||||||||
|
1.000 | 0.120 | 16 | 85985481 | upstream gene variant | T/A | snv | 0.24 |
|
0.800 | 1.000 | 4 | 2012 | 2019 | ||||||||
|
1.000 | 0.120 | 6 | 167127354 | intron variant | C/T | snv | 0.61 |
|
0.800 | 1.000 | 4 | 2012 | 2019 | ||||||||
|
0.790 | 0.320 | 12 | 57574932 | intron variant | C/G | snv | 0.42 |
|
0.820 | 1.000 | 4 | 2008 | 2014 | ||||||||
|
0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 |
|
0.040 | 0.750 | 4 | 2005 | 2013 | ||||||||
|
0.882 | 0.240 | 6 | 32437082 | upstream gene variant | A/G | snv | 0.62 |
|
0.700 | 1.000 | 4 | 2007 | 2011 | ||||||||
|
0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 |
|
0.700 | 1.000 | 4 | 2007 | 2011 | ||||||||
|
1.000 | 0.120 | 5 | 103273223 | intron variant | G/A | snv | 0.24 |
|
0.800 | 1.000 | 4 | 2012 | 2019 | ||||||||
|
0.683 | 0.480 | 8 | 11486464 | upstream gene variant | C/T | snv | 0.25 |
|
0.830 | 1.000 | 4 | 2009 | 2017 | ||||||||
|
0.752 | 0.360 | X | 154010439 | downstream gene variant | C/A | snv |
|
0.040 | 0.500 | 4 | 2010 | 2018 | |||||||||
|
0.752 | 0.400 | 8 | 118952831 | upstream gene variant | T/C | snv | 0.17 |
|
0.040 | 0.250 | 4 | 2014 | 2019 | ||||||||
|
1.000 | 0.120 | 2 | 60897715 | intron variant | T/C | snv | 0.26 |
|
0.800 | 1.000 | 4 | 2012 | 2019 | ||||||||
|
1.000 | 0.120 | 2 | 186656533 | intron variant | C/A;G | snv | 0.28 |
|
0.040 | 0.750 | 4 | 2007 | 2014 | ||||||||
|
0.790 | 0.280 | 5 | 132301616 | intron variant | C/T | snv | 6.9E-02 |
|
0.040 | 0.500 | 4 | 2005 | 2015 | ||||||||
|
0.925 | 0.200 | 1 | 2622185 | intron variant | T/C | snv | 0.40 |
|
0.810 | 0.750 | 4 | 2008 | 2019 | ||||||||
|
0.752 | 0.360 | 6 | 32609603 | intergenic variant | A/G | snv | 0.19 |
|
0.810 | 1.000 | 4 | 2007 | 2018 | ||||||||
|
0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 |
|
0.800 | 1.000 | 4 | 2007 | 2019 | ||||||||
|
1.000 | 0.120 | 15 | 69699078 | non coding transcript exon variant | G/A | snv | 0.35 |
|
0.800 | 1.000 | 4 | 2012 | 2019 | ||||||||
|
0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv |
|
0.730 | 1.000 | 4 | 2010 | 2012 |