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 | 0.925 | 0.040 | 1 | 68431369 | missense variant | C/A | snv | 8.0E-06 | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||
|
4 | 0.882 | 0.040 | 1 | 68431371 | missense variant | C/G | snv | 4.0E-06 | 1.4E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||
|
1 | 1.000 | 0.040 | 1 | 68444607 | missense variant | C/T | snv | 1.6E-05 | 1.3E-04 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.040 | 1 | 68444665 | frameshift variant | A/-;AA | delins | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.040 | 1 | 68431282 | missense variant | C/A | snv | 1.2E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.040 | 1 | 68446713 | missense variant | C/A | snv | 4.8E-05 | 8.4E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.040 | 1 | 68438214 | synonymous variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 1 | 68439568 | missense variant | C/A;T | snv | 3.6E-05; 4.0E-06 | 0.700 | 0 | |||||||
|
4 | 0.851 | 0.080 | 1 | 68429835 | missense variant | G/A | snv | 8.0E-06 | 2.8E-05 | 0.020 | 1.000 | 2 | 2004 | 2015 | |||
|
4 | 0.851 | 0.080 | 1 | 68438228 | missense variant | G/A;T | snv | 1.6E-05 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
|
6 | 0.827 | 0.080 | 1 | 68444858 | missense variant | G/A | snv | 5.6E-05 | 6.3E-05 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||
|
3 | 0.882 | 0.080 | 1 | 68446862 | splice acceptor variant | T/A | snv | 2.0E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
3 | 0.882 | 0.080 | 1 | 68444818 | frameshift variant | AAATTCTGTTATGACGATCC/- | delins | 0.700 | 0 |