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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
16 | 0.790 | 0.400 | 17 | 67893677 | splice donor variant | A/- | delins | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
28 | 0.672 | 0.400 | 13 | 20189511 | stop gained | C/T | snv | 5.8E-04 | 1.1E-04 | 0.700 | 0 | ||||||
|
64 | 0.672 | 0.520 | 3 | 132675903 | missense variant | G/A;T | snv | 1.9E-03; 4.1E-06 | 0.700 | 0 | |||||||
|
33 | 0.701 | 0.240 | 16 | 2176350 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
8 | 0.851 | 0.240 | 1 | 102912180 | inframe deletion | CCTCACCAGATGGGCCAG/- | delins | 0.700 | 0 | ||||||||
|
4 | 1.000 | 2 | 189085204 | missense variant | C/A | snv | 0.700 | 0 | |||||||||
|
10 | 0.827 | 0.160 | 10 | 75024984 | frameshift variant | GGGT/- | del | 0.700 | 0 | ||||||||
|
9 | 0.851 | 0.240 | 11 | 118496323 | frameshift variant | -/G | delins | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.160 | 2 | 222297043 | missense variant | T/A | snv | 0.700 | 0 | ||||||||
|
97 | 0.614 | 0.480 | 9 | 95485875 | splice acceptor variant | C/T | snv | 4.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
27 | 0.763 | 0.320 | 3 | 132671032 | stop gained | C/G;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
9 | 0.882 | 0.160 | 3 | 12604194 | missense variant | G/A;C;T | snv | 0.700 | 0 | ||||||||
|
11 | 0.827 | 0.240 | 1 | 23848684 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
43 | 0.677 | 0.600 | 2 | 25743913 | frameshift variant | G/- | delins | 0.700 | 0 |