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 | 0.200 | 3 | 32973977 | regulatory region variant | G/C;T | snv |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.925 | 0.120 | 3 | 159905770 | intron variant | C/T | snv | 0.32 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.160 | 1 | 192572342 | intron variant | C/A;G;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.080 | 15 | 74804102 | downstream gene variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.882 | 0.200 | 2 | 68371823 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 |
|
0.800 | 1.000 | 1 | 2011 | 2016 | ||||||||
|
0.827 | 0.200 | 3 | 188402113 | intron variant | G/A | snv | 0.61 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 17 | 46788073 | intron variant | T/G | snv | 0.27 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.080 | 3 | 46336534 | intergenic variant | C/T | snv | 0.68 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.827 | 0.240 | 6 | 159069404 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2014 | |||||||||
|
1.000 | 0.080 | 6 | 159051263 | intron variant | G/A | snv | 0.66 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 1 | 172894808 | intron variant | G/A | snv | 0.31 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.807 | 0.240 | 22 | 21628603 | missense variant | C/T | snv | 0.27 | 0.18 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.882 | 0.360 | 6 | 90170316 | intron variant | C/A | snv | 0.72 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 3 | 159957140 | intron variant | T/C | snv | 0.54 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.200 | 1 | 200923009 | intron variant | T/C | snv | 0.53 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.827 | 0.200 | 1 | 2595307 | missense variant | A/G | snv | 0.41 | 0.46 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||
|
0.882 | 0.240 | 6 | 32240547 | intergenic variant | C/A;T | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 10 | 6359663 | intergenic variant | C/A;G;T | snv |
|
0.800 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.882 | 0.200 | 2 | 203937855 | intron variant | T/C | snv | 0.65 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.080 | 3 | 32996229 | downstream gene variant | T/C | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.240 | 21 | 44227538 | 3 prime UTR variant | T/C | snv |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.851 | 0.240 | 22 | 21625000 | downstream gene variant | T/C | snv | 0.19 |
|
0.800 | 1.000 | 1 | 2011 | 2016 | ||||||||
|
1.000 | 0.080 | 14 | 68811487 | intergenic variant | C/T | snv | 0.28 |
|
0.800 | 1.000 | 1 | 2010 | 2010 |