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 | 1 | 11046591 | missense variant | G/A | snv | 9.1E-03 | 3.6E-02 |
|
0.700 | 0 | ||||||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.820 | 1.000 | 9 | 2003 | 2015 | |||||||
|
0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 |
|
0.020 | 1.000 | 2 | 2008 | 2011 | |||||||
|
0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.010 | < 0.001 | 1 | 2008 | 2008 | |||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.776 | 0.360 | 1 | 11046609 | missense variant | T/C | snv | 2.1E-02 | 2.2E-02 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
1 | 11034305 | intron variant | A/G | snv | 8.0E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.040 | 1 | 11027630 | missense variant | C/T | snv | 7.1E-03 | 2.9E-02 |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 1 | 11034982 | intron variant | C/A;T | snv |
|
0.020 | 1.000 | 2 | 2014 | 2015 | |||||||||
|
1.000 | 0.040 | 1 | 11030840 | missense variant | A/G | snv | 5.0E-02 | 5.8E-02 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.807 | 0.240 | 1 | 11030859 | missense variant | C/A | snv | 0.74 | 0.63 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 1 | 11046616 | missense variant | G/A | snv | 6.5E-04 | 6.4E-04 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 1 | 11046616 | missense variant | G/A | snv | 6.5E-04 | 6.4E-04 |
|
0.010 | 1.000 | 1 | 2018 | 2018 |