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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 |
|
0.850 | 0.889 | 2 | 2010 | 2019 | ||||||||
|
0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv |
|
0.820 | 0.667 | 1 | 2011 | 2018 | |||||||||
|
0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 |
|
0.800 | 1.000 | 2 | 2008 | 2019 | ||||||||
|
0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2011 | 2019 | |||||||||
|
0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2011 | 2013 | |||||||||
|
0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 |
|
0.800 | 1.000 | 2 | 2009 | 2019 | ||||||||
|
0.851 | 0.080 | 1 | 154465420 | 3 prime UTR variant | T/A;C | snv | 0.80 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.851 | 0.080 | 1 | 154449591 | intron variant | T/C | snv | 0.60 |
|
0.800 | 1.000 | 1 | 2013 | 2018 | ||||||||
|
0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 |
|
0.700 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 |
|
0.700 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 |
|
0.700 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 2 | 2011 | 2013 | |||||||||
|
0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 2 | 2011 | 2013 | |||||||||
|
1 | 154405860 | intron variant | T/C | snv | 1.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 154405860 | intron variant | T/C | snv | 1.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 154403877 | non coding transcript exon variant | C/T | snv | 0.94 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 154403877 | non coding transcript exon variant | C/T | snv | 0.94 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 154448878 | intron variant | T/C | snv | 9.3E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.160 | 1 | 154446403 | intron variant | C/T | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.160 | 1 | 154427539 | intron variant | G/T | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.851 | 0.080 | 1 | 154449591 | intron variant | T/C | snv | 0.60 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.851 | 0.080 | 1 | 154449591 | intron variant | T/C | snv | 0.60 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1 | 154434943 | intron variant | A/C;T | snv | 0.39; 4.2E-06 |
|
0.700 | 1.000 | 1 | 2011 | 2011 |