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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 21017159 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
2 | 21018633 | intron variant | A/G | snv | 0.14 |
|
0.800 | 1.000 | 2 | 2012 | 2019 | ||||||||||
|
2 | 21018633 | intron variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||||
|
2 | 21017492 | intron variant | A/G | snv | 0.73 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21018633 | intron variant | A/G | snv | 0.14 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||||
|
2 | 21044338 | upstream gene variant | A/G | snv | 0.82 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21044338 | upstream gene variant | A/G | snv | 0.82 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21044338 | upstream gene variant | A/G | snv | 0.82 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
2 | 21036740 | intron variant | A/G | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21036740 | intron variant | A/G | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21036740 | intron variant | A/G | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21014366 | intron variant | A/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21014366 | intron variant | A/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21014366 | intron variant | A/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.689 | 0.280 | 2 | 21006288 | missense variant | C/A;T | snv | 2.8E-04 | 7.3E-04 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | |||||||
|
0.689 | 0.280 | 2 | 21006288 | missense variant | C/A;T | snv | 2.8E-04 | 7.3E-04 |
|
0.800 | 1.000 | 2 | 2012 | 2014 | |||||||
|
0.790 | 0.200 | 2 | 21002881 | stop gained | C/A;T | snv | 8.0E-06; 0.15 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.790 | 0.200 | 2 | 21002881 | stop gained | C/A;T | snv | 8.0E-06; 0.15 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |