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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
1.000 | 0.877 | 13 | 2005 | 2019 | |||||||
|
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 | ||||||||
|
0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 |
|
0.880 | 1.000 | 1 | 2007 | 2016 | ||||||||
|
0.827 | 0.200 | 9 | 120927961 | intron variant | G/A | snv | 0.52 |
|
0.870 | 0.909 | 4 | 2007 | 2015 | ||||||||
|
0.925 | 0.120 | 21 | 44289270 | non coding transcript exon variant | G/A | snv | 0.19 |
|
0.860 | 0.833 | 1 | 2011 | 2019 | ||||||||
|
0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 |
|
0.850 | 0.818 | 6 | 2008 | 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 | ||||||||
|
0.732 | 0.480 | 20 | 46119308 | intron variant | T/A;G | snv |
|
0.840 | 1.000 | 3 | 2008 | 2016 | |||||||||
|
0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 |
|
0.830 | 0.857 | 4 | 2012 | 2019 | |||||||
|
0.662 | 0.440 | 10 | 6057082 | intron variant | T/C | snv | 0.18 |
|
0.830 | 1.000 | 2 | 2012 | 2015 | ||||||||
|
0.925 | 0.160 | 5 | 103261019 | intron variant | C/T | snv | 0.30 |
|
0.830 | 1.000 | 2 | 2010 | 2019 | ||||||||
|
0.683 | 0.480 | 8 | 11486464 | upstream gene variant | C/T | snv | 0.25 |
|
0.830 | 1.000 | 2 | 2009 | 2017 | ||||||||
|
0.827 | 0.280 | 9 | 120944104 | regulatory region variant | T/A;C | snv |
|
0.830 | 1.000 | 2 | 2007 | 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 | ||||||||
|
0.776 | 0.320 | 2 | 203745673 | intergenic variant | C/A;T | snv |
|
0.820 | 0.833 | 4 | 2012 | 2019 | |||||||||
|
0.763 | 0.480 | 6 | 32696074 | intergenic variant | C/A;T | snv |
|
0.820 | 1.000 | 4 | 2007 | 2018 | |||||||||
|
0.790 | 0.200 | 9 | 34710263 | intron variant | G/A;C | snv |
|
0.820 | 1.000 | 3 | 2008 | 2017 | |||||||||
|
0.925 | 0.160 | 4 | 26106575 | downstream gene variant | G/C | snv | 0.29 |
|
0.820 | 1.000 | 3 | 2010 | 2016 | ||||||||
|
0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 |
|
0.820 | 1.000 | 2 | 2010 | 2016 | ||||||||
|
0.790 | 0.320 | 12 | 57574932 | intron variant | C/G | snv | 0.42 |
|
0.820 | 1.000 | 2 | 2008 | 2014 | ||||||||
|
0.851 | 0.280 | 6 | 31654829 | intron variant | C/A | snv | 0.23 |
|
0.820 | 1.000 | 2 | 2011 | 2014 | ||||||||
|
0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 |
|
0.820 | 1.000 | 1 | 2012 | 2017 | ||||||||
|
0.827 | 0.200 | 22 | 37155567 | intron variant | A/G | snv | 0.36 |
|
0.820 | 1.000 | 1 | 2007 | 2014 | ||||||||
|
0.790 | 0.320 | 6 | 32315077 | intron variant | A/G | snv | 0.14 |
|
0.810 | 1.000 | 4 | 2007 | 2016 |