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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.120 | 8 | 1771563 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 8 | 1771518 | missense variant | C/A;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1780472 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
5 | 0.851 | 0.160 | 8 | 1780498 | missense variant | C/G;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 8 | 1771598 | splice donor variant | G/T | snv | 4.0E-06 | 2.1E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 8 | 1780265 | frameshift variant | CT/- | delins | 0.700 | 1.000 | 3 | 2000 | 2012 | |||||
|
1 | 1.000 | 0.120 | 8 | 1771317 | frameshift variant | A/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1771101 | frameshift variant | T/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1771104 | frameshift variant | A/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1771257 | frameshift variant | C/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1780299 | frameshift variant | T/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1771116 | frameshift variant | G/-;GG | delins | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 8 | 1771142 | frameshift variant | G/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1780248 | splice acceptor variant | A/G | snv | 0.700 | 0 | ||||||||
|
4 | 0.882 | 0.160 | 8 | 1771055 | start lost | A/G | snv | 1.2E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 8 | 1771056 | start lost | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1771233 | inframe deletion | AAG/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 1780339 | inframe deletion | TGG/- | delins | 0.700 | 0 |