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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 1 | 116558335 | intron variant | A/G | snv | 0.28 |
|
0.810 | 1.000 | 4 | 2009 | 2018 | ||||||||
|
0.662 | 0.440 | 10 | 6057082 | intron variant | T/C | snv | 0.18 |
|
0.900 | 1.000 | 3 | 2007 | 2019 | ||||||||
|
0.882 | 0.200 | 1 | 116561593 | intron variant | A/G | snv | 0.19 |
|
0.820 | 1.000 | 3 | 2009 | 2018 | ||||||||
|
0.925 | 0.160 | 6 | 32368410 | intron variant | T/C | snv | 0.83 |
|
0.810 | 1.000 | 3 | 2007 | 2018 | ||||||||
|
1.000 | 0.080 | 1 | 116495665 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 2 | 2009 | 2011 | |||||||||
|
1.000 | 0.080 | 12 | 57739473 | intron variant | G/A;T | snv |
|
0.820 | 1.000 | 2 | 2009 | 2018 | |||||||||
|
0.851 | 0.240 | 10 | 79300560 | intron variant | C/A | snv | 0.27 |
|
0.800 | 1.000 | 2 | 2011 | 2019 | ||||||||
|
0.882 | 0.160 | 10 | 6060049 | intron variant | C/T | snv | 0.11 |
|
0.850 | 1.000 | 2 | 2007 | 2018 | ||||||||
|
0.790 | 0.320 | 6 | 159044945 | 5 prime UTR variant | T/C | snv | 0.49 |
|
0.810 | 1.000 | 2 | 2011 | 2017 | ||||||||
|
1.000 | 0.080 | 11 | 60993140 | intron variant | C/A;G | snv |
|
0.850 | 1.000 | 2 | 2009 | 2016 | |||||||||
|
0.776 | 0.360 | 12 | 6330843 | non coding transcript exon variant | T/C | snv | 0.36; 4.0E-06 | 0.38 |
|
0.880 | 1.000 | 2 | 2009 | 2019 | |||||||
|
0.882 | 0.200 | 5 | 159332892 | non coding transcript exon variant | A/G | snv | 0.52 |
|
0.800 | 1.000 | 2 | 2011 | 2011 | ||||||||
|
0.827 | 0.320 | 6 | 32438565 | upstream gene variant | A/C | snv | 0.59 |
|
0.800 | 1.000 | 2 | 2010 | 2013 | ||||||||
|
0.882 | 0.240 | 6 | 32433440 | regulatory region variant | C/T | snv | 0.62 |
|
0.800 | 1.000 | 2 | 2010 | 2010 | ||||||||
|
0.807 | 0.240 | 6 | 32445274 | downstream gene variant | A/G | snv | 0.90 |
|
0.890 | 1.000 | 2 | 2007 | 2018 | ||||||||
|
0.827 | 0.200 | 1 | 2595307 | missense variant | A/G | snv | 0.41 | 0.46 |
|
0.710 | 1.000 | 2 | 2010 | 2011 | |||||||
|
0.851 | 0.240 | 5 | 40392626 | regulatory region variant | T/C | snv | 0.14 |
|
0.800 | 1.000 | 2 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 5 | 40424324 | intron variant | A/C;G | snv | 0.57 |
|
0.800 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.683 | 0.560 | 5 | 35874473 | missense variant | C/T | snv | 0.23 | 0.21 |
|
0.900 | 0.909 | 2 | 2007 | 2018 | |||||||
|
0.925 | 0.080 | 6 | 31279290 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 2 | 2007 | 2010 | |||||||||
|
0.827 | 0.280 | 6 | 127957653 | intergenic variant | A/G;T | snv |
|
0.800 | 1.000 | 2 | 2011 | 2019 | |||||||||
|
0.807 | 0.240 | 6 | 32619077 | intergenic variant | G/A | snv | 0.86 |
|
0.800 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.827 | 0.240 | 11 | 2148913 | intron variant | G/A | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 |
|
0.710 | 0.500 | 1 | 2011 | 2012 | ||||||||
|
1.000 | 0.080 | 2 | 230242009 | intron variant | C/T | snv | 0.13 |
|
0.810 | 1.000 | 1 | 2011 | 2015 |