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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.925 | 0.080 | 11 | 47337496 | missense variant | C/T | snv | 1.5E-03 | 1.2E-03 | 0.800 | 1.000 | 1 | 2010 | 2010 | |||
|
1 | 1.000 | 11 | 47332095 | missense variant | C/A;T | snv | 0.800 | 1.000 | 1 | 2010 | 2010 | ||||||
|
7 | 0.790 | 0.120 | 11 | 47342578 | stop gained | C/A;G | snv | 1.3E-05 | 0.700 | 1.000 | 4 | 1997 | 2013 | ||||
|
6 | 0.807 | 0.080 | 11 | 47335996 | missense variant | G/A;T | snv | 6.8E-05; 7.9E-05 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
|
4 | 0.851 | 0.080 | 11 | 47339323 | splice donor variant | C/A;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.080 | 11 | 47335104 | missense variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
4 | 0.851 | 0.080 | 11 | 47342718 | missense variant | C/T | snv | 2.4E-05 | 4.2E-05 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.080 | 11 | 47342734 | missense variant | C/G;T | snv | 4.0E-06; 2.2E-04 | 0.700 | 0 | |||||||
|
5 | 0.851 | 0.080 | 11 | 47338520 | missense variant | C/G;T | snv | 1.6E-05 | 0.700 | 0 | |||||||
|
3 | 0.882 | 0.080 | 11 | 47332275 | intron variant | AGGGAAGCCATCCAGGCTGAGAGGG/- | delins | 4.0E-03 | 8.9E-04 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.080 | 11 | 47337792 | missense variant | C/T | snv | 4.0E-05 | 3.5E-05 | 0.700 | 0 | ||||||
|
4 | 0.851 | 0.080 | 11 | 47333189 | splice region variant | C/A;G;T | snv | 1.8E-05; 4.4E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.040 | 11 | 47351344 | frameshift variant | TGCCCTCTGTG/- | delins | 7.0E-06 | 0.700 | 0 | |||||||
|
4 | 0.851 | 0.080 | 11 | 47339792 | splice acceptor variant | T/C | snv | 0.700 | 0 | ||||||||
|
4 | 0.851 | 0.080 | 11 | 47335082 | frameshift variant | AG/- | del | 7.0E-06 | 0.700 | 0 | |||||||
|
5 | 0.827 | 0.120 | 11 | 47332075 | stop gained | G/A | snv | 8.1E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
5 | 0.827 | 0.120 | 11 | 47348424 | missense variant | C/T | snv | 1.7E-05 | 4.2E-05 | 0.700 | 0 | ||||||
|
4 | 0.851 | 0.080 | 11 | 47346379 | intron variant | C/T | snv | 2.1E-05 | 0.700 | 0 | |||||||
|
10 | 0.790 | 0.120 | 11 | 47333552 | splice region variant | C/T | snv | 1.7E-05 | 0.700 | 0 | |||||||
|
3 | 0.882 | 0.080 | 11 | 47337544 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 0 |