| 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 | 14 | 100128600 | missense variant | C/T | snv | 1.1E-05 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 2 | 100294302 | missense variant | G/A | snv | 4.1E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 10 | 101002900 | missense variant | G/A | snv | 2.8E-05 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 7 | 101223799 | missense variant | C/T | snv | 2.8E-05 | 4.2E-05 |
|
0.700 | 0 | ||||||||||
|
0.776 | 0.080 | 11 | 101785666 | intron variant | T/A | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 10 | 102109138 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 7 | 102281843 | missense variant | C/T | snv | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.790 | 0.080 | 11 | 10265208 | intron variant | A/C;T | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.742 | 0.160 | 10 | 102835491 | non coding transcript exon variant | G/A | snv | 0.25 |
|
0.710 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.776 | 0.120 | 8 | 103189173 | intron variant | C/T | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.708 | 0.280 | 11 | 103745837 | intron variant | A/G | snv | 5.4E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.708 | 0.280 | 11 | 103813371 | intron variant | A/G | snv | 7.2E-03 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.080 | 9 | 104809521 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 |
|
0.700 | 0 | ||||||||||
|
0.790 | 0.080 | 4 | 105127134 | intergenic variant | T/C | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.790 | 0.080 | 4 | 105143597 | upstream gene variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.763 | 0.240 | 4 | 105207603 | intron variant | G/A | snv | 0.70 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 14 | 105217692 | missense variant | C/T | snv | 4.0E-05 | 4.2E-05 |
|
0.700 | 0 | ||||||||||
|
0.790 | 0.080 | 6 | 105519019 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.080 | MT | 10563 | missense variant | T/C | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 0.080 | 2 | 106331987 | intergenic variant | C/G | snv | 0.84 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.790 | 0.080 | 11 | 106436144 | intergenic variant | T/C | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.776 | 0.080 | 17 | 10803924 | missense variant | G/A;C | snv |
|
0.700 | 1.000 | 3 | 2019 | 2019 | |||||||||
|
1.000 | 0.080 | 4 | 108163645 | missense variant | C/T | snv | 8.0E-06 | 3.5E-05 |
|
0.700 | 0 | ||||||||||
|
0.790 | 0.080 | 13 | 108630682 | intron variant | C/T | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2017 | 2017 |