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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv |
|
0.840 | 1.000 | 5 | 2011 | 2018 | |||||||||
|
0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 |
|
0.810 | 1.000 | 3 | 2011 | 2017 | ||||||||
|
0.790 | 0.200 | 1 | 222650187 | intron variant | A/C;G;T | snv | 0.64; 6.4E-06 |
|
0.840 | 1.000 | 3 | 2007 | 2013 | ||||||||
|
0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv |
|
0.850 | 1.000 | 3 | 2007 | 2018 | |||||||||
|
0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv |
|
0.820 | 1.000 | 2 | 2011 | 2013 | |||||||||
|
0.827 | 0.280 | 12 | 120997784 | synonymous variant | G/A;T | snv | 6.7E-06; 0.40 |
|
0.820 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv |
|
0.830 | 1.000 | 2 | 2007 | 2012 | |||||||||
|
0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv |
|
0.700 | 1.000 | 2 | 2011 | 2011 | |||||||||
|
0.807 | 0.200 | 3 | 138403280 | 3 prime UTR variant | C/A;T | snv |
|
0.800 | 1.000 | 2 | 2009 | 2014 | |||||||||
|
1.000 | 0.040 | 12 | 128194523 | upstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.040 | 9 | 22114496 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.882 | 0.120 | 9 | 22123767 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.040 | 9 | 22106226 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.040 | 6 | 33879300 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 |
|
0.750 | 1.000 | 1 | 2007 | 2018 | ||||||||
|
1.000 | 0.040 | 19 | 10727810 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.040 | 1 | 146039391 | upstream gene variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.708 | 0.280 | 6 | 133893387 | 3 prime UTR variant | C/G;T | snv |
|
0.820 | 1.000 | 1 | 2011 | 2017 | |||||||||
|
1.000 | 0.040 | 4 | 173224875 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.120 | 5 | 90250292 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.925 | 0.120 | 1 | 202500595 | intron variant | T/C | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.724 | 0.480 | 8 | 117172544 | missense variant | C/A;T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 6 | 29473392 | upstream gene variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.790 | 0.240 | 15 | 74785026 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.040 | 8 | 62183763 | intergenic variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 |