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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 1 | 22086463 | missense variant | G/A | snv | 0.700 | 0 | ||||||||||
|
8 | 0.925 | 0.080 | 1 | 22086507 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
6 | 0.925 | 0.080 | 1 | 22086856 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
8 | 0.851 | 0.240 | 1 | 102912180 | inframe deletion | CCTCACCAGATGGGCCAG/- | delins | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.040 | 1 | 145977482 | splice acceptor variant | G/A | snv | 0.700 | 0 | ||||||||
|
16 | 0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
43 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 0.700 | 0 | |||||||
|
5 | 0.882 | 0.120 | 1 | 109272915 | inframe insertion | -/AGAAGAGGAGGA | delins | 5.2E-05 | 4.2E-05 | 0.700 | 0 | ||||||
|
4 | 0.925 | 0.040 | 1 | 145974824 | splice acceptor variant | G/A | snv | 2.3E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
5 | 0.925 | 0.160 | 1 | 244053934 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
3 | 1.000 | 0.160 | 1 | 210920032 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
17 | 0.790 | 0.440 | 2 | 72498492 | stop gained | A/C | snv | 0.700 | 1.000 | 2 | 2013 | 2014 | |||||
|
10 | 0.882 | 0.080 | 2 | 112098688 | missense variant | A/G | snv | 1.6E-05 | 2.1E-05 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||
|
9 | 0.851 | 0.240 | 2 | 100006808 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
10 | 0.882 | 0.080 | 2 | 161423825 | frameshift variant | -/C | delins | 0.700 | 0 | ||||||||
|
7 | 0.882 | 0.120 | 2 | 199272423 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
13 | 0.790 | 0.160 | 2 | 240775863 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
5 | 0.925 | 0.040 | 3 | 114339276 | missense variant | T/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.827 | 0.160 | 3 | 49722056 | missense variant | C/T | snv | 2.9E-04 | 1.8E-04 | 0.700 | 0 | ||||||
|
7 | 0.882 | 0.080 | 3 | 49723632 | missense variant | G/A | snv | 8.0E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
5 | 0.925 | 0.120 | 3 | 129500070 | splice donor variant | T/C | snv | 0.700 | 0 | ||||||||
|
14 | 0.851 | 0.160 | 4 | 55359444 | stop gained | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
13 | 0.807 | 0.200 | 4 | 39218060 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
9 | 0.882 | 0.160 | 4 | 139386152 | stop gained | C/G | snv | 0.700 | 0 | ||||||||
|
4 | 1.000 | 0.080 | 5 | 141955844 | stop gained | C/A | snv | 4.0E-06 | 0.700 | 1.000 | 1 | 2019 | 2019 |