| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
19 | 40236313 | missense variant | T/C | snv |
|
0.700 | 1.000 | 2 | 2005 | 2014 | |||||||||||
|
0.925 | 0.120 | 5 | 112839942 | stop gained | C/G;T | snv | 4.0E-06 |
|
0.700 | 1.000 | 12 | 1992 | 2015 | ||||||||
|
0.925 | 0.120 | 5 | 112839606 | stop gained | C/G;T | snv |
|
0.700 | 1.000 | 8 | 1992 | 2015 | |||||||||
|
5 | 112839693 | stop gained | C/T | snv |
|
0.700 | 1.000 | 7 | 1992 | 2015 | |||||||||||
|
5 | 112839879 | stop gained | C/A;T | snv |
|
0.700 | 1.000 | 7 | 1992 | 2014 | |||||||||||
|
5 | 112839729 | stop gained | G/T | snv |
|
0.700 | 1.000 | 5 | 1992 | 2015 | |||||||||||
|
5 | 112839726 | stop gained | C/T | snv |
|
0.700 | 1.000 | 5 | 1994 | 2014 | |||||||||||
|
0.851 | 0.120 | 5 | 112838934 | stop gained | C/A;T | snv | 8.0E-06 |
|
0.700 | 1.000 | 5 | 1990 | 2014 | ||||||||
|
0.882 | 0.120 | 5 | 112838220 | stop gained | C/A;T | snv |
|
0.700 | 1.000 | 4 | 1992 | 2014 | |||||||||
|
5 | 112839510 | stop gained | G/A;T | snv |
|
0.700 | 1.000 | 4 | 1992 | 2015 | |||||||||||
|
0.763 | 0.280 | 15 | 44711547 | start lost | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.763 | 0.280 | 15 | 44711549 | start lost | G/A | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.763 | 0.280 | 15 | 44711548 | start lost | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 |
|
0.790 | 0.970 | 24 | 2002 | 2019 | ||||||||
|
0.677 | 0.400 | 7 | 140753354 | missense variant | T/A;C;G | snv |
|
0.700 | 1.000 | 8 | 2002 | 2016 | |||||||||
|
0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.700 | 1.000 | 7 | 2002 | 2016 | ||||||||
|
0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.700 | 1.000 | 7 | 2002 | 2016 | ||||||||
|
0.807 | 0.280 | 7 | 140753349 | missense variant | C/A;G;T | snv |
|
0.700 | 1.000 | 7 | 2002 | 2014 | |||||||||
|
0.882 | 0.080 | 7 | 140753338 | inframe insertion | -/TAG | delins | 4.0E-06 |
|
0.700 | 1.000 | 6 | 2009 | 2012 | ||||||||
|
0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.763 | 0.360 | 7 | 140753393 | missense variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.790 | 0.360 | 7 | 140754187 | missense variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.763 | 0.360 | 7 | 140753355 | missense variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.807 | 0.200 | 9 | 21974678 | missense variant | C/A | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.742 | 0.280 | 9 | 21971120 | missense variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 |