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 | 0.280 | 8 | 116847620 | inframe deletion | GTT/- | delins | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
10 | 0.827 | 0.160 | 11 | 71444952 | start lost | T/C | snv | 1.2E-05; 4.0E-06 | 3.5E-05 | 0.700 | 0 | ||||||
|
15 | 0.827 | 0.240 | 18 | 55229003 | frameshift variant | -/ATTG | delins | 0.700 | 0 | ||||||||
|
34 | 0.716 | 0.400 | 19 | 13136099 | missense variant | C/A;T | snv | 0.700 | 0 | ||||||||
|
73 | 0.641 | 0.560 | 17 | 75494905 | frameshift variant | -/A | delins | 4.0E-06 | 0.700 | 0 | |||||||
|
14 | 0.763 | 0.160 | 4 | 5748226 | stop gained | C/A;T | snv | 3.2E-05; 1.2E-05 | 0.700 | 0 | |||||||
|
73 | 0.641 | 0.560 | 17 | 75489265 | splice acceptor variant | G/C | snv | 0.700 | 0 | ||||||||
|
20 | 0.827 | 0.200 | 14 | 77025671 | frameshift variant | C/- | delins | 0.700 | 0 | ||||||||
|
10 | 0.851 | 0.320 | 11 | 119278162 | splice acceptor variant | AAAG/- | del | 0.700 | 0 | ||||||||
|
46 | 0.689 | 0.480 | 7 | 92501562 | missense variant | C/T | snv | 3.2E-04 | 3.5E-04 | 0.700 | 0 | ||||||
|
12 | 0.790 | 0.160 | 4 | 5719239 | intron variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 0.700 | 0 | |||||||
|
10 | 0.790 | 0.200 | 6 | 79026079 | stop gained | G/A;C | snv | 0.700 | 0 | ||||||||
|
14 | 0.752 | 0.280 | 1 | 119915813 | frameshift variant | G/-;GG | delins | 0.700 | 0 | ||||||||
|
17 | 0.776 | 0.280 | 9 | 92718565 | missense variant | G/A;T | snv | 0.700 | 0 |