ALK, ALK receptor tyrosine kinase, 238
N. diseases: 519; N. variants: 41
Source: ALL
Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.160 | 2 | 29222407 | missense variant | G/A;C | snv | 3.2E-05 |
|
0.800 | 1.000 | 4 | 2008 | 2011 | ||||||||
|
1.000 | 2 | 29209873 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 |
|
0.800 | 1.000 | 4 | 2008 | 2011 | ||||||||
|
0.763 | 0.240 | 2 | 29220831 | missense variant | A/C;G;T | snv |
|
0.800 | 1.000 | 4 | 2008 | 2011 | |||||||||
|
0.925 | 0.040 | 2 | 29213994 | missense variant | A/C;G;T | snv |
|
0.800 | 1.000 | 4 | 2008 | 2011 | |||||||||
|
0.925 | 0.080 | 2 | 29222584 | missense variant | C/G | snv |
|
0.800 | 0 | ||||||||||||
|
0.776 | 0.200 | 2 | 29220829 | missense variant | G/C;T | snv |
|
0.800 | 0 | ||||||||||||
|
1.000 | 2 | 29222362 | missense variant | A/C;G | snv |
|
0.700 | 1.000 | 4 | 2008 | 2011 | ||||||||||
|
0.776 | 0.120 | 2 | 29220830 | missense variant | A/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.120 | 2 | 29222347 | missense variant | A/G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.120 | 2 | 29209798 | missense variant | C/A;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.120 | 2 | 29220776 | missense variant | C/G;T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 2 | 29214009 | missense variant | A/C | snv |
|
0.700 | 0 | |||||||||||||
|
0.925 | 0.080 | 2 | 29213993 | missense variant | A/C | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 2 | 29213992 | missense variant | G/C;T | snv |
|
0.700 | 0 | |||||||||||||
|
0.851 | 0.080 | 2 | 29209789 | missense variant | T/G | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | 2 | 29223430 | missense variant | C/T | snv | 7.0E-06 |
|
0.700 | 0 |