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 | 0.080 | 9 | 79337213 | intergenic variant | C/G;T | snv |
|
0.800 | 1.000 | 3 | 2010 | 2017 | |||||||||
|
0.925 | 0.160 | 12 | 65781114 | intron variant | G/C;T | snv |
|
0.810 | 1.000 | 3 | 2010 | 2017 | |||||||||
|
1.000 | 0.080 | 6 | 20679079 | intron variant | T/G | snv | 0.41 |
|
0.700 | 1.000 | 3 | 2007 | 2011 | ||||||||
|
0.925 | 0.080 | 9 | 8879118 | intron variant | C/T | snv | 0.14 |
|
0.820 | 1.000 | 3 | 2010 | 2016 | ||||||||
|
1.000 | 0.080 | 4 | 6301295 | missense variant | C/A;G;T | snv | 0.67 |
|
0.810 | 1.000 | 3 | 2010 | 2018 | ||||||||
|
0.925 | 0.120 | 15 | 89831025 | 3 prime UTR variant | C/A | snv | 0.72 |
|
0.820 | 1.000 | 3 | 2011 | 2018 | ||||||||
|
0.882 | 0.200 | 11 | 2837316 | intron variant | C/T | snv | 8.1E-02 |
|
0.880 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 60357684 | intron variant | G/A | snv | 0.45 |
|
0.820 | 1.000 | 3 | 2010 | 2017 | ||||||||
|
0.882 | 0.160 | 17 | 2312964 | intron variant | T/C | snv | 0.58 |
|
0.820 | 1.000 | 3 | 2010 | 2018 | ||||||||
|
0.882 | 0.120 | 2 | 164645339 | intergenic variant | A/C;G;T | snv |
|
0.810 | 1.000 | 3 | 2011 | 2017 | |||||||||
|
0.790 | 0.280 | 17 | 37738049 | intron variant | A/G | snv | 0.52 |
|
0.870 | 1.000 | 3 | 2009 | 2019 | ||||||||
|
0.882 | 0.120 | 3 | 64726228 | intron variant | C/T | snv | 0.28 |
|
0.840 | 1.000 | 3 | 2008 | 2019 | ||||||||
|
0.925 | 0.120 | 6 | 20657333 | intron variant | A/G | snv | 0.41 |
|
0.830 | 1.000 | 3 | 2009 | 2019 | ||||||||
|
0.925 | 0.120 | 20 | 44360627 | intron variant | G/A | snv | 0.18 |
|
0.830 | 1.000 | 3 | 2011 | 2017 | ||||||||
|
0.925 | 0.120 | 3 | 185812502 | intron variant | T/C | snv | 0.46 |
|
0.810 | 1.000 | 3 | 2008 | 2012 | ||||||||
|
0.882 | 0.080 | 2 | 226155937 | TF binding site variant | A/G | snv | 0.36 |
|
0.820 | 1.000 | 3 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 8 | 94948283 | intron variant | T/C | snv | 0.45 |
|
0.810 | 1.000 | 3 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 6 | 20641105 | intron variant | C/T | snv | 0.13 |
|
0.800 | 1.000 | 3 | 2010 | 2013 | ||||||||
|
0.882 | 0.120 | 6 | 20717024 | intron variant | T/C | snv | 0.30 |
|
0.830 | 1.000 | 3 | 2007 | 2017 | ||||||||
|
1.000 | 0.080 | 3 | 23162533 | regulatory region variant | T/C | snv | 0.21 |
|
0.700 | 1.000 | 3 | 2010 | 2013 | ||||||||
|
0.827 | 0.240 | 9 | 4292083 | intron variant | G/A | snv | 0.45 |
|
0.800 | 1.000 | 2 | 2012 | 2014 | ||||||||
|
1.000 | 0.080 | 10 | 113048313 | intron variant | T/C | snv | 0.54 |
|
0.720 | 1.000 | 2 | 2007 | 2015 | ||||||||
|
1.000 | 0.080 | 6 | 20717173 | intron variant | A/G | snv | 0.30 |
|
0.700 | 1.000 | 2 | 2010 | 2011 | ||||||||
|
1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 |
|
0.800 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.925 | 0.120 | 12 | 54705212 | intergenic variant | T/A | snv | 0.76 |
|
0.810 | 1.000 | 2 | 2008 | 2012 |