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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
13 | 0.807 | 0.240 | 19 | 49596253 | stop gained | G/T | snv | 0.700 | 0 | ||||||||
|
14 | 0.851 | 0.160 | 4 | 55359444 | stop gained | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
19 | 0.763 | 0.280 | 8 | 60850546 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.160 | 8 | 93765413 | stop gained | C/T | snv | 8.0E-06 | 2.1E-05 | 0.700 | 0 | ||||||
|
7 | 0.790 | 0.200 | 21 | 43172104 | missense variant | C/A;T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
|
5 | 0.851 | 0.160 | 4 | 182754413 | missense variant | C/A;G | snv | 4.2E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
5 | 0.851 | 0.160 | 4 | 182799938 | missense variant | C/T | snv | 9.2E-06 | 1.4E-05 | 0.700 | 0 | ||||||
|
13 | 0.776 | 0.200 | 6 | 10398693 | frameshift variant | TT/- | delins | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.080 | 8 | 143816613 | frameshift variant | TGGCCTTATGA/- | delins | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.120 | 19 | 49595234 | frameshift variant | -/ACCACCC | delins | 0.700 | 0 | ||||||||
|
16 | 0.776 | 0.280 | 19 | 49601646 | frameshift variant | TGCC/- | delins | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.120 | 8 | 93804851 | inframe insertion | -/TATGAA | delins | 0.700 | 0 |