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 | 1.000 | 0.080 | 9 | 132311820 | frameshift variant | CTCT/-;CT | delins | 4.0E-06; 2.4E-05 | 3.5E-05 | 0.700 | 0 | ||||||
|
15 | 0.790 | 0.120 | 15 | 79845388 | missense variant | C/T | snv | 3.2E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
5 | 0.925 | 0.080 | 10 | 100988947 | missense variant | A/G | snv | 1.6E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
16 | 0.776 | 0.240 | 15 | 89649836 | missense variant | T/G | snv | 1.3E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
15 | 0.790 | 0.120 | 15 | 79845338 | stop gained | G/A | snv | 2.0E-05 | 3.5E-05 | 0.700 | 0 | ||||||
|
5 | 0.851 | 0.160 | 16 | 1587209 | missense variant | C/T | snv | 2.0E-05 | 0.700 | 0 | |||||||
|
2 | 1.000 | 6 | 146159536 | stop gained | C/A;T | snv | 1.6E-05 | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.120 | 12 | 106496115 | missense variant | C/A;T | snv | 4.0E-06 | 2.1E-05 | 0.700 | 0 | ||||||
|
4 | 1.000 | 0.080 | 9 | 133352441 | splice region variant | C/A;T | snv | 2.4E-05 | 0.700 | 0 | |||||||
|
9 | 0.827 | 0.160 | 9 | 133351970 | frameshift variant | AG/- | delins | 8.4E-05 | 0.700 | 0 | |||||||
|
2 | 1.000 | 0.160 | 8 | 60232322 | stop gained | T/A;C | snv | 0.700 | 0 | ||||||||
|
7 | 0.851 | 0.200 | 16 | 8806398 | missense variant | C/G;T | snv | 4.0E-06; 2.4E-05 | 0.700 | 0 | |||||||
|
4 | 0.925 | 0.200 | 22 | 50083183 | intron variant | A/G;T | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
8 | 0.827 | 0.280 | 18 | 23538564 | missense variant | G/C | snv | 1.2E-04 | 2.1E-04 | 0.700 | 0 | ||||||
|
10 | 0.827 | 0.160 | 9 | 128203609 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.080 | 19 | 13230185 | missense variant | T/G | snv | 0.010 | 1.000 | 1 | 1998 | 1998 | |||||
|
4 | 0.882 | 0.160 | 9 | 69053240 | missense variant | G/T | snv | 0.010 | 1.000 | 1 | 1999 | 1999 | |||||
|
17 | 0.776 | 0.320 | 8 | 63065904 | splice region variant | C/A;T | snv | 2.0E-05 | 0.010 | 1.000 | 1 | 1999 | 1999 | ||||
|
3 | 0.925 | 0.120 | X | 75070499 | missense variant | C/A;G | snv | 0.010 | 1.000 | 1 | 2001 | 2001 | |||||
|
4 | 0.925 | 0.080 | 19 | 53889705 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
|
3 | 1.000 | 0.080 | 19 | 53889655 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
|
3 | 1.000 | 0.080 | 9 | 132327718 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
6 | 0.827 | 0.160 | 22 | 50625392 | missense variant | G/A | snv | 3.9E-04 | 3.6E-04 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
31 | 0.701 | 0.360 | 15 | 89327201 | missense variant | C/T | snv | 5.1E-04 | 6.7E-04 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
7 | 0.882 | 0.160 | 11 | 6393301 | missense variant | T/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2007 | 2007 |