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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.776 | 0.360 | 10 | 92703125 | intergenic variant | C/T | snv | 0.36 |
|
0.900 | 0.914 | 8 | 2007 | 2020 | ||||||||
|
0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 |
|
0.900 | 0.939 | 6 | 2009 | 2020 | ||||||||
|
0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 |
|
0.800 | 1.000 | 2 | 2012 | 2018 | ||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.780 | 1.000 | 1 | 2006 | 2018 | ||||||||
|
0.776 | 0.280 | 11 | 2160994 | splice region variant | A/T | snv | 0.73 | 0.60 |
|
0.720 | 1.000 | 1 | 2016 | 2019 | |||||||
|
0.776 | 0.280 | 17 | 37741165 | intron variant | C/T | snv | 0.41 |
|
0.720 | 1.000 | 1 | 2010 | 2019 | ||||||||
|
0.790 | 0.320 | 11 | 2818521 | intron variant | C/T | snv | 9.2E-02 |
|
0.900 | 1.000 | 6 | 2008 | 2019 | ||||||||
|
0.790 | 0.280 | 18 | 60217517 | intergenic variant | G/A | snv | 0.21 |
|
0.840 | 1.000 | 4 | 2009 | 2018 | ||||||||
|
0.790 | 0.280 | 17 | 37738049 | intron variant | A/G | snv | 0.52 |
|
0.870 | 1.000 | 3 | 2009 | 2019 | ||||||||
|
0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv |
|
0.900 | 0.889 | 2 | 2008 | 2019 | |||||||||
|
0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv |
|
0.870 | 0.900 | 1 | 2006 | 2020 | |||||||||
|
0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.807 | 0.200 | 6 | 20661019 | intron variant | G/A;C;T | snv |
|
0.900 | 0.958 | 5 | 2007 | 2019 | |||||||||
|
0.807 | 0.240 | 2 | 43505684 | missense variant | T/C | snv | 9.9E-02 | 0.14 |
|
0.840 | 1.000 | 2 | 2008 | 2017 | |||||||
|
0.807 | 0.160 | 1 | 182112825 | intron variant | C/T | snv | 0.36 |
|
0.730 | 1.000 | 1 | 2013 | 2016 | ||||||||
|
0.807 | 0.240 | 6 | 123540174 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.807 | 0.200 | 11 | 92940662 | downstream gene variant | C/G;T | snv |
|
0.880 | 1.000 | 1 | 2009 | 2019 | |||||||||
|
0.807 | 0.280 | 8 | 128555832 | intron variant | C/T | snv | 0.65 |
|
0.800 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.807 | 0.240 | 8 | 35265058 | intron variant | C/T | snv | 5.1E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.807 | 0.240 | 6 | 36026129 | upstream gene variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.807 | 0.240 | 4 | 53790270 | intron variant | G/A | snv | 2.5E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.807 | 0.240 | 6 | 36030611 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.807 | 0.200 | 7 | 28154778 | intron variant | C/A;T | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.827 | 0.160 | 11 | 17387083 | missense variant | C/T | snv | 0.64 | 0.71 |
|
0.860 | 0.941 | 7 | 2007 | 2018 | |||||||
|
0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv |
|
0.900 | 0.966 | 6 | 2007 | 2019 |