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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
10 | 0.851 | 0.120 | 16 | 9768994 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
35 | 0.716 | 0.320 | 9 | 97687208 | inframe deletion | ATTCTT/- | delins | 0.700 | 0 | ||||||||
|
35 | 0.716 | 0.320 | 9 | 97675476 | frameshift variant | AGTCTTACGGTACA/- | delins | 6.8E-05 | 6.3E-05 | 0.700 | 0 | ||||||
|
16 | 0.776 | 0.240 | 15 | 89649836 | missense variant | T/G | snv | 1.3E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
8 | 0.827 | 0.200 | 11 | 89284940 | missense variant | A/G | snv | 1.9E-04 | 2.2E-04 | 0.700 | 0 | ||||||
|
9 | 0.807 | 0.200 | 11 | 89178218 | missense variant | T/C | snv | 4.0E-06 | 2.1E-05 | 0.700 | 0 | ||||||
|
34 | 0.716 | 0.520 | 16 | 8901028 | frameshift variant | CT/- | delins | 0.700 | 0 | ||||||||
|
22 | 0.752 | 0.320 | 16 | 8811153 | missense variant | G/A | snv | 4.1E-03 | 3.7E-03 | 0.700 | 0 | ||||||
|
12 | 0.807 | 0.280 | 16 | 8801859 | missense variant | G/A;C;T | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
19 | 0.790 | 0.240 | 14 | 87988523 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
20 | 0.776 | 0.240 | 14 | 87968393 | missense variant | C/T | snv | 8.0E-06 | 2.8E-05 | 0.700 | 0 | ||||||
|
13 | 0.851 | 0.240 | 17 | 81934931 | missense variant | C/T | snv | 2.4E-05 | 4.2E-05 | 0.700 | 0 | ||||||
|
10 | 0.790 | 0.200 | 6 | 79026079 | stop gained | G/A;C | snv | 0.700 | 0 | ||||||||
|
9 | 0.827 | 0.240 | 17 | 7586766 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
12 | 0.807 | 0.280 | 17 | 7586699 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
11 | 0.776 | 0.480 | 16 | 75541466 | non coding transcript exon variant | A/G | snv | 4.2E-06 | 0.700 | 0 | |||||||
|
73 | 0.641 | 0.560 | 17 | 75494905 | frameshift variant | -/A | delins | 4.0E-06 | 0.700 | 0 | |||||||
|
73 | 0.641 | 0.560 | 17 | 75489265 | splice acceptor variant | G/C | snv | 0.700 | 0 | ||||||||
|
5 | 0.925 | 0.120 | 3 | 70977675 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
8 | 0.827 | 0.280 | 15 | 66436843 | missense variant | A/G | snv | 4.0E-06 | 0.700 | 1.000 | 7 | 2006 | 2009 | ||||
|
28 | 0.716 | 0.520 | 20 | 58903703 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
7 | 0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins | 0.700 | 0 | ||||||||
|
15 | 0.827 | 0.240 | 18 | 55229003 | frameshift variant | -/ATTG | delins | 0.700 | 0 | ||||||||
|
24 | 0.708 | 0.400 | X | 53647576 | splice acceptor variant | T/C | snv | 0.700 | 0 | ||||||||
|
5 | 0.851 | 0.280 | X | 53615815 | missense variant | C/T | snv | 0.700 | 0 |