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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 21 | 37490353 | frameshift variant | -/A | delins | 0.700 | 0 | ||||||||||
|
5 | 0.925 | 0.040 | 8 | 143817380 | frameshift variant | -/C | delins | 0.700 | 0 | ||||||||
|
34 | 0.752 | 0.240 | 4 | 25145129 | splice acceptor variant | -/C | delins | 4.2E-05 | 0.700 | 0 | |||||||
|
6 | 21 | 37490451 | frameshift variant | -/G | delins | 0.700 | 0 | ||||||||||
|
6 | 21 | 37496249 | frameshift variant | -/G | delins | 0.700 | 0 | ||||||||||
|
46 | 0.742 | 0.480 | 19 | 35718020 | frameshift variant | -/GGCGGGCGGCGGC | delins | 0.700 | 0 | ||||||||
|
13 | 0.851 | 0.120 | 8 | 41934340 | frameshift variant | -/T | delins | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
5 | 0.882 | 0.160 | 8 | 143817668 | frameshift variant | -/TTTT | delins | 0.700 | 0 | ||||||||
|
30 | 0.742 | 0.560 | 1 | 1806503 | missense variant | A/C;G;T | snv | 4.0E-06 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
4 | 1.000 | 10 | 79216266 | missense variant | A/G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
8 | 0.882 | 0.080 | 6 | 98875675 | missense variant | A/G | snv | 1.2E-05 | 1.4E-05 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||
|
14 | 0.827 | 0.200 | 1 | 1804565 | missense variant | A/G | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
10 | 0.776 | 0.320 | 8 | 60781285 | frameshift variant | AA/T | delins | 0.700 | 0 | ||||||||
|
10 | 0.925 | 3 | 9741340 | frameshift variant | AG/T | delins | 0.700 | 0 | |||||||||
|
33 | 0.732 | 0.480 | 22 | 23833670 | inframe deletion | AGA/- | delins | 0.700 | 0 | ||||||||
|
25 | 0.827 | 0.120 | 13 | 28672407 | frameshift variant | AT/- | delins | 0.700 | 0 | ||||||||
|
14 | 0.882 | 0.080 | 9 | 92719007 | inframe deletion | ATT/- | del | 0.700 | 0 | ||||||||
|
45 | 0.724 | 0.440 | 7 | 39950821 | frameshift variant | C/- | delins | 0.700 | 0 | ||||||||
|
50 | 0.672 | 0.560 | 16 | 30737343 | stop gained | C/A;T | snv | 0.700 | 0 | ||||||||
|
43 | 0.683 | 0.480 | 10 | 102657073 | stop gained | C/A;T | snv | 0.700 | 0 | ||||||||
|
19 | 0.807 | 0.280 | 1 | 26773716 | stop gained | C/G;T | snv | 0.700 | 0 | ||||||||
|
23 | 0.742 | 0.440 | 2 | 121530892 | non coding transcript exon variant | C/G;T | snv | 7.7E-06; 2.3E-05; 3.5E-04 | 0.700 | 0 | |||||||
|
44 | 0.701 | 0.600 | 13 | 23886338 | missense variant | C/G;T | snv | 4.8E-06; 9.6E-06 | 0.700 | 0 | |||||||
|
4 | 0.882 | 0.200 | 2 | 39007168 | missense variant | C/T | snv | 0.700 | 1.000 | 3 | 2007 | 2007 | |||||
|
45 | 0.708 | 0.440 | 19 | 1242559 | missense variant | C/T | snv | 6.7E-06 | 0.700 | 1.000 | 1 | 2018 | 2018 |