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 | 0.080 | 11 | 111742586 | missense variant | A/G | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 11 | 111766340 | missense variant | C/G;T | snv | 2.0E-04 | 5.2E-04 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 11 | 111753514 | missense variant | A/G | snv | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 |
|
0.700 | 0 | ||||||||||
|
0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 11 | 111743419 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.925 | 0.040 | 11 | 111709215 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 2 | 2013 | 2017 | |||||||||
|
0.925 | 0.040 | 11 | 111709215 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 11 | 111765903 | 5 prime UTR variant | T/G | snv | 0.71 | 0.75 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
11 | 111763868 | intron variant | C/A | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
11 | 111715367 | intron variant | C/G | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
11 | 111716226 | intron variant | G/A | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
11 | 111734491 | intron variant | T/C | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 111752364 | intron variant | T/A | snv | 0.71 | 0.75 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |