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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.763 | 0.480 | 13 | 110179387 | missense variant | C/A | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.120 | 1 | 17157671 | intergenic variant | G/T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.120 | 13 | 37047903 | stop gained | T/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.320 | 1 | 160837925 | intron variant | T/C | snv | 0.57 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.200 | 1 | 113877706 | 3 prime UTR variant | C/A;T | snv |
|
0.710 | 0.500 | 1 | 2009 | 2010 | |||||||||
|
0.742 | 0.480 | 16 | 10877045 | intron variant | G/A | snv | 0.53 |
|
0.780 | 0.625 | 0 | 2006 | 2012 | ||||||||
|
0.701 | 0.480 | 6 | 31574699 | upstream gene variant | C/A | snv | 0.14 |
|
0.720 | 0.667 | 1 | 2011 | 2019 | ||||||||
|
0.851 | 0.200 | 11 | 36503743 | intron variant | C/G;T | snv |
|
0.720 | 0.667 | 1 | 2012 | 2019 | |||||||||
|
0.882 | 0.120 | 2 | 60854407 | intron variant | C/T | snv | 0.35 |
|
0.720 | 0.667 | 1 | 2009 | 2014 | ||||||||
|
0.925 | 0.200 | 1 | 2622185 | intron variant | T/C | snv | 0.40 |
|
0.810 | 0.750 | 3 | 2008 | 2019 | ||||||||
|
0.581 | 0.680 | 20 | 46118343 | 5 prime UTR variant | T/C | snv | 0.75 | 0.80 |
|
0.730 | 0.750 | 1 | 2012 | 2017 | |||||||
|
0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 |
|
0.850 | 0.818 | 6 | 2008 | 2019 | ||||||||
|
0.776 | 0.320 | 2 | 203745673 | intergenic variant | C/A;T | snv |
|
0.820 | 0.833 | 4 | 2012 | 2019 | |||||||||
|
0.925 | 0.120 | 21 | 44289270 | non coding transcript exon variant | G/A | snv | 0.19 |
|
0.860 | 0.833 | 1 | 2011 | 2019 | ||||||||
|
0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 |
|
0.830 | 0.857 | 4 | 2012 | 2019 | |||||||
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
1.000 | 0.877 | 13 | 2005 | 2019 | |||||||
|
0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 |
|
0.850 | 0.889 | 4 | 2010 | 2019 | ||||||||
|
0.827 | 0.200 | 9 | 120927961 | intron variant | G/A | snv | 0.52 |
|
0.870 | 0.909 | 4 | 2007 | 2015 | ||||||||
|
0.742 | 0.440 | 6 | 137685367 | intron variant | G/A | snv | 0.16 |
|
0.900 | 0.938 | 6 | 2007 | 2019 | ||||||||
|
0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 |
|
0.900 | 0.966 | 3 | 2007 | 2017 | ||||||||
|
0.925 | 0.200 | 6 | 32827255 | 3 prime UTR variant | G/A | snv | 6.1E-02 |
|
0.800 | 1.000 | 4 | 2007 | 2016 | ||||||||
|
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 | ||||||||
|
0.742 | 0.280 | 21 | 42434957 | missense variant | A/C;G | snv | 0.27; 8.0E-06 |
|
0.820 | 1.000 | 4 | 2014 | 2019 | ||||||||
|
0.882 | 0.240 | 6 | 32437082 | upstream gene variant | A/G | snv | 0.62 |
|
0.700 | 1.000 | 4 | 2007 | 2011 |