| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.683 | 0.320 | 15 | 48465820 | stop gained | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.683 | 0.280 | 8 | 115604339 | stop gained | G/A;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.689 | 0.320 | 7 | 40046006 | missense variant | A/G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.716 | 0.360 | 12 | 109800665 | missense variant | C/T | snv |
|
0.700 | 1.000 | 4 | 2010 | 2014 | |||||||||
|
0.716 | 0.360 | 9 | 136433182 | missense variant | G/A;T | snv | 3.4E-05; 4.2E-06 |
|
0.700 | 0 | |||||||||||
|
0.732 | 0.240 | 16 | 70496367 | missense variant | C/G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.742 | 0.120 | 1 | 26697152 | frameshift variant | -/GCCGCCTCCCTCCTCCAGCGCC | delins |
|
0.700 | 0 | ||||||||||||
|
0.752 | 0.280 | 1 | 119915813 | frameshift variant | G/-;GG | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.120 | 2 | 142918608 | splice acceptor variant | G/T | snv | 1.4E-04 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.776 | 0.240 | 22 | 18078405 | frameshift variant | C/-;CC | delins |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 18 | 10714931 | splice acceptor variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 18 | 10795003 | splice acceptor variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.360 | 4 | 15587929 | splice donor variant | G/- | delins | 1.9E-04 |
|
0.700 | 0 | |||||||||||
|
0.790 | 0.360 | 10 | 95637327 | missense variant | C/A;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.320 | 11 | 71441307 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
0.807 | 0.320 | 11 | 71435840 | splice acceptor variant | C/A;G | snv | 5.6E-05; 3.9E-03 |
|
0.700 | 0 | |||||||||||
|
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 | |||||||||||
|
0.807 | 0.160 | 1 | 173828312 | non coding transcript exon variant | TT/C | delins |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.200 | 12 | 116007542 | stop gained | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.160 | 4 | 122207168 | stop gained | T/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.160 | 9 | 131506164 | inframe deletion | CTT/- | delins | 3.2E-05 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
0.851 | 0.160 | 10 | 75030037 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.120 | 16 | 81357848 | missense variant | C/G;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.851 | 0.120 | 3 | 146079255 | missense variant | C/A | snv | 4.0E-06 | 1.4E-05 |
|
0.700 | 0 | ||||||||||
|
0.851 | 0.120 | 3 | 146071125 | stop gained | G/A | snv |
|
0.700 | 0 |