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 | 0.120 | 6 | 32697982 | intergenic variant | -/TTCGTC;TTCGTCAGAC | delins |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.925 | 0.120 | 6 | 31353908 | 3 prime UTR variant | A/C | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.120 | 12 | 111270654 | non coding transcript exon variant | A/C | snv | 0.30 |
|
0.810 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.160 | 6 | 32379017 | intron variant | A/C | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.120 | 6 | 32955131 | intron variant | A/C | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.120 | 9 | 16801852 | intron variant | A/C | snv | 8.5E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.120 | 6 | 30759162 | intron variant | A/C | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.827 | 0.320 | 6 | 32438565 | upstream gene variant | A/C | snv | 0.59 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.807 | 0.320 | 6 | 32408694 | upstream gene variant | A/C | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.925 | 0.160 | 7 | 50959497 | intron variant | A/C | snv | 0.96 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
1.000 | 0.120 | 11 | 2172610 | upstream gene variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.925 | 0.160 | 6 | 32837132 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.925 | 0.160 | 6 | 32714360 | upstream gene variant | A/C;G | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.851 | 0.360 | 6 | 32158225 | non coding transcript exon variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.925 | 0.160 | 6 | 30353412 | downstream gene variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
1.000 | 0.120 | 6 | 31296684 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
1.000 | 0.120 | 13 | 75752146 | intron variant | A/C;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.807 | 0.320 | 16 | 11086016 | intron variant | A/G | snv | 0.37 |
|
0.800 | 1.000 | 4 | 2007 | 2011 | ||||||||
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
1.000 | 0.950 | 4 | 2004 | 2020 | |||||||
|
0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 |
|
0.810 | 1.000 | 3 | 2007 | 2010 | ||||||||
|
0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 |
|
0.830 | 0.667 | 2 | 2009 | 2019 | ||||||||
|
0.851 | 0.200 | 6 | 31642909 | missense variant | A/G | snv | 0.51 | 0.44 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.882 | 0.200 | 6 | 31642752 | non coding transcript exon variant | A/G | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2007 | 2007 |