| 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 | ||||||||
|
0.882 | 0.200 | 1 | 116561593 | intron variant | A/G | snv | 0.19 |
|
0.820 | 1.000 | 4 | 2009 | 2018 | ||||||||
|
1.000 | 0.080 | 1 | 116495665 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 2 | 2009 | 2011 | |||||||||
|
0.882 | 0.160 | 1 | 192571891 | intron variant | G/A | snv | 0.86 |
|
0.800 | 1.000 | 2 | 2011 | 2019 | ||||||||
|
0.827 | 0.200 | 1 | 2595307 | missense variant | A/G | snv | 0.41 | 0.46 |
|
0.710 | 1.000 | 2 | 2010 | 2011 | |||||||
|
1.000 | 0.080 | 1 | 10293054 | intron variant | T/C | snv | 0.32 |
|
0.830 | 1.000 | 1 | 2008 | 2011 | ||||||||
|
1.000 | 0.080 | 1 | 92655550 | intron variant | G/C | snv | 0.57 |
|
0.710 | 1.000 | 1 | 2011 | 2017 | ||||||||
|
0.851 | 0.080 | 1 | 2569783 | non coding transcript exon variant | G/T | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.925 | 0.120 | 1 | 161502368 | upstream gene variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.882 | 0.200 | 1 | 24977085 | intergenic variant | A/G | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 1 | 198861813 | intron variant | T/C | snv | 1.2E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.080 | 1 | 100941963 | non coding transcript exon variant | A/G | snv | 0.28 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.827 | 0.200 | 1 | 200966738 | downstream gene variant | T/C | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.160 | 1 | 116720516 | regulatory region variant | C/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 1 | 85449500 | intron variant | T/C | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 1 | 92607671 | missense variant | C/A | snv | 0.20 | 0.20 |
|
0.710 | 1.000 | 1 | 2010 | 2016 | |||||||
|
1.000 | 0.080 | 1 | 92682820 | intron variant | C/T | snv | 0.20 |
|
0.810 | 1.000 | 1 | 2011 | 2017 | ||||||||
|
1.000 | 0.080 | 1 | 100865980 | intergenic variant | T/C | snv | 0.48 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 1 | 85281310 | intron variant | C/T | snv | 8.4E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 1 | 201015352 | intron variant | G/A | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.160 | 1 | 192572342 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 1 | 92362948 | intron variant | A/C | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.925 | 0.160 | 1 | 157800451 | intron variant | C/T | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 |