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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 |
|
0.900 | 1.000 | 3 | 2007 | 2019 | ||||||||
|
0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 |
|
0.900 | 0.905 | 1 | 2008 | 2019 | ||||||||
|
0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 |
|
0.900 | 1.000 | 1 | 2007 | 2019 | ||||||||
|
0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 |
|
0.890 | 0.800 | 1 | 2010 | 2019 | ||||||||
|
0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv |
|
0.890 | 1.000 | 1 | 2007 | 2016 | |||||||||
|
0.925 | 0.120 | 16 | 28871920 | missense variant | A/G;T | snv | 0.35 |
|
0.880 | 0.778 | 1 | 2011 | 2015 | ||||||||
|
0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv |
|
0.860 | 0.889 | 1 | 2011 | 2014 | |||||||||
|
0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv |
|
0.840 | 1.000 | 1 | 2007 | 2012 | |||||||||
|
0.925 | 0.120 | 18 | 23560468 | missense variant | T/C | snv | 0.33 | 0.29 |
|
0.830 | 1.000 | 1 | 2009 | 2013 | |||||||
|
0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 |
|
0.820 | 0.833 | 3 | 2008 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 16257952 | intergenic variant | C/A;T | snv |
|
0.810 | 1.000 | 1 | 2009 | 2013 | |||||||||
|
0.882 | 0.120 | 9 | 28414341 | intron variant | A/G | snv | 0.26 |
|
0.810 | 1.000 | 1 | 2012 | 2013 | ||||||||
|
0.925 | 0.120 | 9 | 28425517 | intron variant | C/G | snv | 0.26 |
|
0.810 | 1.000 | 1 | 2013 | 2019 | ||||||||
|
1.000 | 0.080 | 16 | 79648854 | regulatory region variant | T/C | snv | 0.44 |
|
0.810 | 1.000 | 1 | 2009 | 2013 | ||||||||
|
0.925 | 0.120 | 3 | 186106215 | intron variant | T/C | snv | 0.86 |
|
0.810 | 1.000 | 1 | 2013 | 2019 | ||||||||
|
0.827 | 0.160 | 19 | 45678134 | missense variant | G/C | snv | 0.18 | 0.17 |
|
0.810 | 1.000 | 1 | 2013 | 2019 | |||||||
|
0.882 | 0.160 | 1 | 72299433 | intron variant | G/A;C | snv |
|
0.810 | 1.000 | 1 | 2013 | 2014 | |||||||||
|
0.925 | 0.080 | 11 | 66127695 | intron variant | A/G | snv | 0.46 |
|
0.810 | 1.000 | 1 | 2013 | 2017 | ||||||||
|
0.925 | 0.120 | 16 | 53788739 | intron variant | A/G;T | snv |
|
0.810 | 1.000 | 1 | 2011 | 2019 | |||||||||
|
0.925 | 0.120 | 16 | 53779538 | intron variant | A/T | snv | 0.40 |
|
0.810 | 1.000 | 1 | 2011 | 2015 | ||||||||
|
0.925 | 0.160 | 11 | 27541835 | intron variant | G/A;T | snv |
|
0.810 | 1.000 | 1 | 2011 | 2018 | |||||||||
|
1.000 | 0.080 | 16 | 53791576 | intron variant | C/T | snv | 0.34 |
|
0.810 | 1.000 | 1 | 2009 | 2017 | ||||||||
|
1.000 | 0.080 | 1 | 72285502 | intron variant | T/C | snv | 0.62 |
|
0.800 | 1.000 | 2 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 2 | 24927427 | intergenic variant | A/G | snv | 0.57 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.882 | 0.120 | 2 | 646364 | intergenic variant | T/A | snv | 0.82 |
|
0.800 | 1.000 | 1 | 2013 | 2013 |