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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
24 | 0.708 | 0.400 | X | 53647576 | splice acceptor variant | T/C | snv | 0.700 | 0 | ||||||||
|
31 | 0.742 | 0.440 | 1 | 40290871 | frameshift variant | T/-;TT | delins | 0.700 | 0 | ||||||||
|
10 | 0.776 | 0.400 | 3 | 189868624 | missense variant | C/G | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
13 | 0.790 | 0.440 | X | 53537626 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.807 | 0.400 | 10 | 75025250 | splice donor variant | G/A | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
12 | 0.827 | 0.240 | 19 | 49835897 | frameshift variant | C/- | delins | 1.2E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
10 | 0.827 | 0.160 | 10 | 75024984 | frameshift variant | GGGT/- | del | 0.700 | 0 | ||||||||
|
16 | 0.827 | 0.120 | 12 | 45850644 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
12 | 0.827 | 0.240 | 19 | 49829816 | missense variant | C/T | snv | 8.7E-06 | 0.700 | 0 | |||||||
|
5 | 0.851 | 0.280 | X | 53615815 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.120 | 1 | 21864095 | splice region variant | C/T | snv | 0.700 | 0 | ||||||||
|
6 | 0.925 | 0.240 | 6 | 157181040 | frameshift variant | AA/- | delins | 0.700 | 0 | ||||||||
|
6 | 0.925 | 0.240 | 6 | 157200866 | frameshift variant | -/T | delins | 0.700 | 0 | ||||||||
|
6 | 0.925 | 0.240 | 6 | 157167101 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
6 | 0.925 | 0.240 | 6 | 157110496 | frameshift variant | CCG/TCCGCAGCCACTCC | delins | 0.700 | 0 |