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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 1.000 | 11 | 128810620 | frameshift variant | ATTA/- | delins | 0.700 | 0 | |||||||||
|
9 | 0.807 | 0.120 | 17 | 56848773 | stop gained | G/A | snv | 9.1E-05 | 1.5E-04 | 0.700 | 0 | ||||||
|
20 | 0.763 | 0.280 | 15 | 82240555 | missense variant | T/C | snv | 8.2E-06 | 0.700 | 0 | |||||||
|
5 | 1 | 22086463 | missense variant | G/A | snv | 0.700 | 0 | ||||||||||
|
4 | 0.882 | 0.160 | 6 | 79925034 | splice acceptor variant | T/C | snv | 0.700 | 0 | ||||||||
|
8 | 0.882 | 0.160 | 9 | 133426240 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
8 | 0.882 | 0.160 | 9 | 133442718 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 10 | 27100445 | 5 prime UTR variant | G/C | snv | 0.700 | 0 | ||||||||
|
10 | 0.827 | 0.360 | X | 124365758 | splice region variant | C/G | snv | 0.700 | 0 | ||||||||
|
1 | 21 | 34859476 | missense variant | C/T | snv | 0.700 | 0 | ||||||||||
|
2 | 1.000 | 0.120 | 21 | 34859477 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
12 | 0.790 | 0.320 | 16 | 8811660 | missense variant | T/C | snv | 2.9E-04 | 4.1E-04 | 0.700 | 0 | ||||||
|
10 | 0.790 | 0.240 | 1 | 9726972 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
33 | 0.667 | 0.360 | 22 | 28695869 | frameshift variant | G/- | del | 2.0E-03 | 1.8E-03 | 0.700 | 0 | ||||||
|
2 | 1.000 | 0.120 | X | 48794162 | stop lost | T/C | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.120 | 16 | 1449081 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
3 | 1.000 | 0.120 | 12 | 11885921 | coding sequence variant | GAACA/- | delins | 0.700 | 0 | ||||||||
|
14 | 0.776 | 0.360 | 16 | 8811088 | stop gained | C/A;T | snv | 4.4E-05; 5.4E-06 | 0.700 | 0 | |||||||
|
11 | 0.882 | 0.200 | 22 | 36292059 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
3 | 1.000 | 17 | 35557404 | missense variant | A/T | snv | 0.700 | 0 | |||||||||
|
3 | 1.000 | 17 | 35557406 | missense variant | T/A | snv | 0.700 | 0 | |||||||||
|
5 | 0.882 | 0.240 | 1 | 155239655 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
5 | 0.925 | 0.160 | 1 | 155236292 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
188 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 0.030 | 1.000 | 3 | 2018 | 2019 | |||
|
9 | 0.807 | 0.080 | 12 | 6019472 | missense variant | C/G;T | snv | 4.0E-06 | 0.030 | 1.000 | 3 | 2010 | 2017 |