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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.200 | 19 | 45352765 | missense variant | G/A | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.200 | 2 | 69193414 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.925 | 0.200 | 1 | 241858594 | missense variant | C/T | snv | 8.0E-05 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.752 | 0.280 | 14 | 103699003 | missense variant | C/G;T | snv | 4.3E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.827 | 0.200 | 8 | 89955487 | missense variant | T/C | snv | 1.2E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.200 | 1 | 241860647 | missense variant | T/C | snv | 1.2E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.200 | 2 | 69182599 | missense variant | G/A | snv | 1.6E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.200 | 12 | 109568774 | missense variant | T/C | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.851 | 0.200 | 19 | 54983029 | missense variant | G/A;T | snv | 7.5E-05; 4.2E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.732 | 0.360 | 19 | 45364096 | missense variant | C/T | snv | 2.6E-05 | 1.4E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.925 | 0.200 | 3 | 9759215 | missense variant | C/A;T | snv | 8.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.200 | 1 | 241858654 | missense variant | G/A;T | snv | 8.0E-06; 8.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.851 | 0.200 | 13 | 102858296 | missense variant | C/G | snv | 2.4E-05 | 1.4E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.925 | 0.200 | 8 | 89981502 | missense variant | C/G;T | snv | 1.6E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.200 | 8 | 89970379 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.200 | 17 | 34991822 | missense variant | A/G | snv | 1.2E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.763 | 0.240 | 16 | 13932175 | missense variant | C/G | snv |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||||
|
0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv |
|
0.010 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.851 | 0.080 | 19 | 45398021 | missense variant | G/C | snv | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.851 | 0.080 | 19 | 45421317 | missense variant | G/C | snv | 1.4E-05 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.851 | 0.080 | 20 | 50082836 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.925 | 0.120 | 7 | 99665170 | synonymous variant | T/A;C | snv | 4.0E-06; 4.0E-06 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.080 | 11 | 108364109 | intron variant | A/C;T | snv |
|
0.010 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
0.882 | 0.160 | 11 | 108334154 | intron variant | C/T | snv | 0.27 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.695 | 0.360 | 10 | 94781859 | synonymous variant | G/A;C | snv | 0.18 |
|
0.010 | 1.000 | 1 | 2007 | 2007 |