Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
60 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
16 | 0.763 | 0.360 | 16 | 68329105 | stop gained | G/C;T | snv | 4.0E-06; 1.6E-05 | 0.700 | 0 | |||||||
|
15 | 0.827 | 0.240 | 18 | 55229003 | frameshift variant | -/ATTG | delins | 0.700 | 0 | ||||||||
|
8 | 0.851 | 0.240 | 15 | 28211095 | frameshift variant | G/- | delins | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.280 | 2 | 1484815 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
13 | 0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
9 | 0.851 | 0.240 | 2 | 100006808 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 1 | 27548302 | stop gained | G/A;C | snv | 0.700 | 0 | ||||||||
|
12 | 0.827 | 0.240 | 19 | 49835897 | frameshift variant | C/- | delins | 1.2E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
6 | 0.827 | 0.400 | X | 77520832 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
15 | 0.776 | 0.360 | 16 | 68355785 | stop gained | C/A | snv | 8.1E-06 | 0.700 | 0 | |||||||
|
9 | 0.851 | 0.320 | X | 53534144 | missense variant | C/G;T | snv | 9.5E-06 | 0.700 | 0 | |||||||
|
43 | 0.752 | 0.360 | 2 | 229830831 | frameshift variant | A/- | delins | 0.700 | 0 | ||||||||
|
11 | 0.807 | 0.240 | 9 | 95459653 | frameshift variant | C/GGGTCCACAACATCT | delins | 0.700 | 0 | ||||||||
|
11 | 0.882 | 0.240 | 12 | 13569973 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.240 | 14 | 28768345 | frameshift variant | T/- | delins | 0.700 | 0 | ||||||||
|
24 | 0.752 | 0.360 | X | 41346607 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
4 | 0.882 | 0.160 | X | 123634002 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
4 | 0.882 | 0.240 | X | 53534615 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.280 | X | 53536580 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
6 | 0.851 | 0.240 | X | 53536600 | missense variant | T/A | snv | 0.700 | 0 | ||||||||
|
13 | 0.790 | 0.440 | X | 53537626 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.280 | X | 53591113 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
5 | 0.851 | 0.280 | X | 53615815 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
7 | 0.925 | 0.240 | X | 53634235 | splice donor variant | C/G | snv | 0.700 | 0 |