Source: ALL
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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.200 | 10 | 100989823 | missense variant | G/C | snv | 0.800 | 1.000 | 12 | 2001 | 2011 | |||||
|
2 | 1.000 | 0.200 | 10 | 100989285 | missense variant | G/A;T | snv | 0.800 | 1.000 | 12 | 2001 | 2011 | |||||
|
1 | 1.000 | 0.200 | 10 | 100989822 | stop gained | G/A;T | snv | 0.800 | 1.000 | 12 | 2001 | 2011 | |||||
|
1 | 1.000 | 0.200 | 10 | 100989154 | stop gained | G/A;T | snv | 0.800 | 1.000 | 12 | 2001 | 2011 | |||||
|
1 | 1.000 | 0.200 | 10 | 100989271 | missense variant | G/A;C | snv | 4.0E-06 | 0.800 | 1.000 | 12 | 2001 | 2011 | ||||
|
2 | 1.000 | 0.200 | 10 | 100989352 | missense variant | T/C;G | snv | 0.800 | 1.000 | 12 | 2001 | 2011 | |||||
|
1 | 1.000 | 0.200 | 10 | 100989316 | missense variant | C/A;G;T | snv | 4.0E-06 | 0.800 | 1.000 | 12 | 2001 | 2011 | ||||
|
1 | 1.000 | 0.200 | 10 | 100989118 | missense variant | G/A;C | snv | 1.2E-05 | 0.800 | 1.000 | 12 | 2001 | 2011 | ||||
|
1 | 1.000 | 0.200 | 10 | 100989294 | missense variant | G/C | snv | 0.700 | 1.000 | 12 | 2001 | 2011 | |||||
|
10 | 0.807 | 0.320 | 10 | 100989331 | missense variant | G/A | snv | 0.700 | 1.000 | 12 | 2001 | 2011 | |||||
|
2 | 1.000 | 0.200 | 10 | 100989774 | splice acceptor variant | G/T | snv | 0.700 | 1.000 | 12 | 2001 | 2011 | |||||
|
2 | 0.925 | 0.240 | 10 | 100989165 | missense variant | A/C;G | snv | 0.800 | 1.000 | 12 | 2001 | 2011 | |||||
|
1 | 1.000 | 0.200 | 10 | 100989320 | missense variant | C/G | snv | 0.700 | 1.000 | 12 | 2001 | 2011 | |||||
|
5 | 0.827 | 0.240 | 10 | 100989280 | missense variant | G/A;C | snv | 2.0E-05 | 0.700 | 1.000 | 4 | 2007 | 2013 | ||||
|
2 | 0.925 | 0.200 | 10 | 100989835 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.200 | 10 | 100989821 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.200 | 10 | 100989117 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.200 | 10 | 100989330 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 0.700 | 0 |