| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.807 | 0.160 | X | 101401752 | missense variant | C/G;T | snv | 5.5E-04 |
|
0.860 | 1.000 | 51 | 1989 | 2018 | ||||||||
|
0.776 | 0.280 | X | 101398942 | missense variant | T/C | snv | 5.5E-06 |
|
0.860 | 1.000 | 50 | 1989 | 2018 | ||||||||
|
0.882 | 0.160 | X | 101398467 | missense variant | C/A;T | snv |
|
0.840 | 1.000 | 50 | 1989 | 2019 | |||||||||
|
1.000 | 0.160 | X | 101403846 | missense variant | G/A | snv |
|
0.830 | 1.000 | 37 | 1989 | 2019 | |||||||||
|
1.000 | 0.160 | X | 101403843 | missense variant | A/G;T | snv |
|
0.830 | 1.000 | 14 | 2002 | 2020 | |||||||||
|
1.000 | 0.160 | X | 101407710 | missense variant | C/G | snv |
|
0.820 | 1.000 | 32 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101398074 | missense variant | C/T | snv | 9.4E-06 |
|
0.810 | 1.000 | 38 | 1989 | 2017 | ||||||||
|
1.000 | 0.160 | X | 101407786 | missense variant | G/A | snv |
|
0.810 | 1.000 | 33 | 1989 | 2017 | |||||||||
|
0.925 | 0.200 | X | 101397871 | missense variant | T/C | snv |
|
0.810 | 1.000 | 31 | 1989 | 2017 | |||||||||
|
0.925 | 0.200 | X | 101401713 | missense variant | C/T | snv |
|
0.810 | 1.000 | 31 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101398018 | missense variant | C/G;T | snv |
|
0.810 | 1.000 | 31 | 1989 | 2020 | |||||||||
|
1.000 | 0.160 | X | 101398078 | stop gained | C/A;T | snv |
|
0.810 | 1.000 | 13 | 1999 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101407780 | missense variant | T/C;G | snv | 9.4E-06 |
|
0.810 | 1.000 | 11 | 2002 | 2017 | ||||||||
|
1.000 | 0.160 | X | 101403908 | missense variant | A/G;T | snv |
|
0.810 | 1.000 | 2 | 2009 | 2016 | |||||||||
|
1.000 | 0.160 | X | 101398033 | missense variant | G/A | snv |
|
0.800 | 1.000 | 43 | 1989 | 2017 | |||||||||
|
0.776 | 0.280 | X | 101403984 | missense variant | C/G | snv | 1.2E-04 | 1.9E-05 |
|
0.800 | 0.976 | 42 | 1989 | 2018 | |||||||
|
1.000 | 0.160 | X | 101398906 | missense variant | C/G;T | snv |
|
0.800 | 1.000 | 38 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101398795 | missense variant | T/A | snv |
|
0.800 | 1.000 | 34 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101407779 | missense variant | A/G | snv |
|
0.800 | 1.000 | 34 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101401695 | missense variant | A/G | snv |
|
0.800 | 1.000 | 33 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101403845 | missense variant | C/A;T | snv | 1.1E-05 |
|
0.800 | 1.000 | 33 | 1989 | 2017 | ||||||||
|
1.000 | 0.160 | X | 101407803 | missense variant | T/C | snv |
|
0.800 | 1.000 | 32 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101398785 | missense variant | C/T | snv |
|
0.800 | 1.000 | 32 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101398387 | missense variant | C/G;T | snv |
|
0.800 | 1.000 | 30 | 1989 | 2017 | |||||||||
|
1.000 | 0.160 | X | 101407738 | missense variant | A/C | snv |
|
0.800 | 1.000 | 30 | 1989 | 2017 |