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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 |
|
0.790 | 0.900 | 10 | 2009 | 2018 | ||||||||
|
0.641 | 0.680 | 6 | 32184665 | upstream gene variant | A/G | snv | 0.15 |
|
0.720 | 0.667 | 3 | 2015 | 2019 | ||||||||
|
5 | 94600780 | intron variant | A/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
14 | 51148434 | intergenic variant | T/C | snv | 0.74 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
11 | 23153770 | upstream gene variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
0.776 | 0.280 | 7 | 142749077 | upstream gene variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
16 | 4922962 | intron variant | C/T | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
10 | 118394924 | intron variant | T/C | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
3 | 55162885 | downstream gene variant | C/A | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
11 | 23193334 | intron variant | A/G | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
21 | 34366284 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
11 | 23133679 | intergenic variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
17 | 49277423 | intron variant | A/C | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
7 | 142802725 | 3 prime UTR variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
11 | 23211338 | intergenic variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
16 | 4982458 | intron variant | C/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
16 | 4979496 | intron variant | A/G | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
17 | 49370810 | non coding transcript exon variant | T/C | snv | 0.11 | 0.30 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
2 | 216433482 | intron variant | A/G | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
11 | 23174695 | intron variant | G/C;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
16 | 4941276 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
16 | 4973520 | intron variant | C/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
21 | 34469442 | intron variant | C/A | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
0.851 | 0.120 | 12 | 3060327 | intergenic variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |