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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
22 | 0.790 | 0.160 | 18 | 10714931 | splice acceptor variant | C/T | snv | 0.700 | 0 | ||||||||
|
22 | 0.790 | 0.160 | 18 | 10795003 | splice acceptor variant | C/T | snv | 0.700 | 0 | ||||||||
|
9 | 0.882 | 0.120 | 12 | 109798819 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
17 | 0.716 | 0.360 | 12 | 109800665 | missense variant | C/T | snv | 0.700 | 1.000 | 4 | 2010 | 2014 | |||||
|
56 | 0.683 | 0.280 | 8 | 115604339 | stop gained | G/A;T | snv | 0.700 | 0 | ||||||||
|
14 | 0.827 | 0.200 | 12 | 116007542 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
14 | 0.752 | 0.280 | 1 | 119915813 | frameshift variant | G/-;GG | delins | 0.700 | 0 | ||||||||
|
6 | 0.827 | 0.160 | 4 | 122207168 | stop gained | T/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 124129992 | intron variant | T/C | snv | 0.23 | 0.710 | 1.000 | 1 | 2014 | 2014 | ||||
|
12 | 0.827 | 0.160 | 9 | 131506164 | inframe deletion | CTT/- | delins | 3.2E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
10 | 0.925 | 0.120 | 9 | 134798410 | frameshift variant | C/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 5 | 135028925 | frameshift variant | GCCGTACGGGCAAGCGCCCGGCGACATGGCCGAGT/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 5 | 135031290 | missense variant | C/T | snv | 0.810 | 1.000 | 2 | 2008 | 2012 | |||||
|
18 | 0.716 | 0.360 | 9 | 136433182 | missense variant | G/A;T | snv | 3.4E-05; 4.2E-06 | 0.700 | 0 | |||||||
|
14 | 0.776 | 0.120 | 2 | 142918608 | splice acceptor variant | G/T | snv | 1.4E-04 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
9 | 0.851 | 0.120 | 3 | 146071125 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
9 | 0.851 | 0.120 | 3 | 146079255 | missense variant | C/A | snv | 4.0E-06 | 1.4E-05 | 0.700 | 0 | ||||||
|
7 | 0.882 | 0.200 | 4 | 15516757 | splice donor variant | G/A | snv | 0.700 | 0 | ||||||||
|
11 | 0.790 | 0.360 | 4 | 15587929 | splice donor variant | G/- | delins | 1.9E-04 | 0.700 | 0 | |||||||
|
14 | 0.807 | 0.160 | 1 | 173828312 | non coding transcript exon variant | TT/C | delins | 0.700 | 0 | ||||||||
|
14 | 0.807 | 0.160 | 1 | 173831632 | splice donor variant | T/A;C;G | snv | 8.0E-06; 3.3E-04; 4.0E-06 | 0.700 | 0 | |||||||
|
14 | 0.776 | 0.240 | 22 | 18078405 | frameshift variant | C/-;CC | delins | 0.700 | 0 | ||||||||
|
15 | 0.742 | 0.120 | 1 | 26697152 | frameshift variant | -/GCCGCCTCCCTCCTCCAGCGCC | delins | 0.700 | 0 | ||||||||
|
5 | 0.882 | 0.200 | 19 | 38499961 | missense variant | T/A | snv | 2.0E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
54 | 0.689 | 0.320 | 7 | 40046006 | missense variant | A/G | snv | 0.700 | 1.000 | 1 | 2017 | 2017 |