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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 1 | 171636359 | missense variant | G/A | snv | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 1 | 171636584 | missense variant | A/G | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.807 | 0.040 | 1 | 171652139 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 1 | 171652236 | missense variant | G/A | snv | 1.5E-04 | 1.3E-04 |
|
0.700 | 0 | ||||||||||
|
0.925 | 0.040 | 1 | 171652454 | missense variant | A/G | snv | 6.4E-05 | 2.1E-05 |
|
0.700 | 0 | ||||||||||
|
0.851 | 0.040 | 1 | 171638703 | missense variant | G/A;C | snv | 4.0E-06; 7.6E-04 |
|
0.700 | 0 | |||||||||||
|
0.807 | 0.080 | 1 | 171636310 | missense variant | G/A | snv | 2.0E-05 | 3.5E-05 |
|
0.700 | 0 | ||||||||||
|
0.925 | 0.040 | 1 | 171636542 | missense variant | C/T | snv | 3.2E-05 | 2.1E-05 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.040 | 1 | 171636709 | missense variant | C/A | snv | 2.5E-05 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.040 | 1 | 171636032 | missense variant | G/A | snv | 2.0E-05 | 1.4E-05 |
|
0.700 | 0 | ||||||||||
|
0.763 | 0.120 | 2 | 38071251 | missense variant | C/T | snv | 5.8E-03 | 1.7E-03 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.040 | 1 | 171636659 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.040 | 1 | 171636349 | missense variant | C/A | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.882 | 0.040 | 1 | 171636302 | missense variant | C/G | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.807 | 0.120 | 1 | 171636131 | missense variant | A/G | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.776 | 0.080 | 1 | 171636331 | missense variant | G/A | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.882 | 0.040 | 1 | 171636010 | missense variant | A/C;T | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.882 | 0.040 | 1 | 171636000 | missense variant | G/T | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.851 | 0.040 | 1 | 171636341 | missense variant | C/T | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
1.000 | 0.040 | 1 | 171636430 | missense variant | T/C | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.851 | 0.040 | 1 | 171636173 | missense variant | T/C | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.882 | 0.040 | 1 | 171636143 | missense variant | A/G | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.807 | 0.120 | 1 | 171652468 | missense variant | C/A | snv | 9.8E-04 | 1.3E-04 |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||
|
1.000 | 0.040 | 1 | 171636706 | missense variant | C/T | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 | |||||||||
|
0.851 | 0.040 | 1 | 171636686 | missense variant | C/T | snv |
|
0.800 | 1.000 | 20 | 1997 | 2007 |