| 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 | 0.320 | 12 | 12718165 | missense variant | T/A;C;G | snv | 1.6E-04; 1.6E-05; 0.26 |
|
0.020 | 1.000 | 2 | 2013 | 2015 | ||||||||
|
0.851 | 0.120 | 2 | 176177905 | non coding transcript exon variant | A/C;T | snv |
|
0.020 | 1.000 | 2 | 2012 | 2017 | |||||||||
|
0.807 | 0.200 | 14 | 64301584 | splice region variant | C/A;T | snv |
|
0.020 | 1.000 | 2 | 2018 | 2019 | |||||||||
|
0.620 | 0.400 | 19 | 45409478 | stop gained | C/A;G;T | snv | 0.29; 4.3E-06; 4.3E-06 |
|
0.020 | 1.000 | 2 | 2014 | 2019 | ||||||||
|
0.827 | 0.200 | 9 | 16915023 | upstream gene variant | T/C | snv | 0.41 |
|
0.020 | 1.000 | 2 | 2011 | 2012 | ||||||||
|
0.882 | 0.120 | 11 | 2150371 | intron variant | T/C | snv | 0.19 |
|
0.020 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.649 | 0.440 | 12 | 53968051 | non coding transcript exon variant | G/A | snv | 0.93 |
|
0.020 | 1.000 | 2 | 2016 | 2018 | ||||||||
|
0.882 | 0.120 | 18 | 676008 | intron variant | G/C | snv | 0.63 |
|
0.020 | 1.000 | 2 | 2010 | 2018 | ||||||||
|
0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 |
|
0.020 | 1.000 | 2 | 2014 | 2016 | |||||||
|
0.776 | 0.160 | 7 | 74059952 | missense variant | G/A;C | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 2012 | 2012 | ||||||||
|
0.708 | 0.240 | 2 | 48962782 | missense variant | C/T | snv | 0.57 | 0.57 |
|
0.020 | 1.000 | 2 | 2009 | 2014 | |||||||
|
0.925 | 0.120 | 9 | 133279871 | upstream gene variant | T/C | snv | 0.49 |
|
0.020 | 1.000 | 2 | 2014 | 2017 | ||||||||
|
0.807 | 0.160 | 17 | 43104122 | missense variant | C/A;G | snv | 1.2E-05 |
|
0.020 | 1.000 | 2 | 2003 | 2012 | ||||||||
|
0.576 | 0.760 | 12 | 47845054 | intron variant | C/A | snv | 0.51 | 0.55 |
|
0.020 | 1.000 | 2 | 2007 | 2013 | |||||||
|
0.763 | 0.200 | 17 | 43094776 | missense variant | C/T | snv | 8.0E-06 |
|
0.020 | 1.000 | 2 | 2005 | 2013 | ||||||||
|
0.724 | 0.160 | 19 | 17278895 | synonymous variant | G/A | snv | 0.15 | 0.18 |
|
0.020 | 1.000 | 2 | 2010 | 2016 | |||||||
|
0.677 | 0.280 | 3 | 37020356 | missense variant | A/G | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv |
|
0.020 | 1.000 | 2 | 2012 | 2015 | |||||||||
|
0.633 | 0.480 | 12 | 53966448 | intron variant | G/A | snv | 0.57 |
|
0.020 | 1.000 | 2 | 2017 | 2018 | ||||||||
|
0.925 | 0.120 | 4 | 69591303 | intron variant | T/C | snv | 0.75 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.851 | 0.120 | 8 | 128531703 | intron variant | G/A | snv | 0.13 |
|
0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.882 | 0.120 | 8 | 128546982 | intron variant | C/T | snv | 7.6E-02 |
|
0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 7 | 35307237 | intergenic variant | G/A | snv | 0.47 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 |
|
0.010 | 1.000 | 1 | 2015 | 2015 |