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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.200 | 1 | 247424492 | missense variant | C/T | snv |
|
0.700 | 1.000 | 10 | 2002 | 2016 | |||||||||
|
0.851 | 0.120 | 1 | 247424765 | missense variant | C/T | snv |
|
0.800 | 1.000 | 7 | 2001 | 2014 | |||||||||
|
0.807 | 0.280 | 1 | 247424041 | missense variant | G/A;C | snv | 8.3E-03; 4.0E-06 |
|
0.800 | 1.000 | 7 | 2001 | 2014 | ||||||||
|
1.000 | 0.080 | 1 | 247425329 | missense variant | A/G | snv |
|
0.800 | 1.000 | 7 | 2001 | 2014 | |||||||||
|
0.851 | 0.080 | 1 | 247424227 | stop gained | C/T | snv |
|
0.800 | 1.000 | 7 | 2001 | 2014 | |||||||||
|
1.000 | 0.080 | 1 | 247425167 | missense variant | T/C | snv |
|
0.800 | 1.000 | 7 | 2002 | 2014 | |||||||||
|
0.882 | 0.080 | 1 | 247424356 | missense variant | G/A;C | snv |
|
0.800 | 1.000 | 7 | 2002 | 2014 | |||||||||
|
1.000 | 0.080 | 1 | 247424375 | missense variant | T/C | snv |
|
0.800 | 1.000 | 7 | 2002 | 2014 | |||||||||
|
1.000 | 0.080 | 1 | 247424912 | missense variant | G/A;C | snv | 6.4E-04; 4.0E-06 |
|
0.700 | 1.000 | 7 | 2001 | 2014 | ||||||||
|
0.851 | 0.200 | 1 | 247424492 | missense variant | C/T | snv |
|
0.820 | 1.000 | 7 | 2001 | 2016 | |||||||||
|
0.851 | 0.200 | 1 | 247424492 | missense variant | C/T | snv |
|
0.700 | 1.000 | 7 | 2002 | 2014 | |||||||||
|
0.851 | 0.120 | 1 | 247424765 | missense variant | C/T | snv |
|
0.710 | 1.000 | 6 | 2001 | 2016 | |||||||||
|
0.807 | 0.280 | 1 | 247424041 | missense variant | G/A;C | snv | 8.3E-03; 4.0E-06 |
|
0.720 | 1.000 | 6 | 2001 | 2014 | ||||||||
|
0.882 | 0.080 | 1 | 247424356 | missense variant | G/A;C | snv |
|
0.810 | 1.000 | 6 | 2001 | 2016 | |||||||||
|
1.000 | 0.080 | 1 | 247424504 | missense variant | C/T | snv |
|
0.800 | 1.000 | 5 | 2001 | 2014 | |||||||||
|
0.851 | 0.080 | 1 | 247424227 | stop gained | C/T | snv |
|
0.820 | 1.000 | 5 | 2001 | 2014 | |||||||||
|
1.000 | 0.080 | 1 | 247425154 | missense variant | G/A;C | snv |
|
0.800 | 1.000 | 5 | 2001 | 2014 | |||||||||
|
0.882 | 0.080 | 1 | 247424356 | missense variant | G/A;C | snv |
|
0.710 | 1.000 | 5 | 2002 | 2014 | |||||||||
|
1.000 | 0.080 | 1 | 247423230 | missense variant | G/C;T | snv | 4.0E-06 |
|
0.040 | 1.000 | 4 | 2015 | 2019 | ||||||||
|
0.689 | 0.560 | 1 | 247425556 | missense variant | C/A | snv | 3.9E-02 | 3.3E-02 |
|
0.040 | 0.500 | 4 | 2010 | 2017 | |||||||
|
0.695 | 0.480 | 1 | 247448734 | 3 prime UTR variant | G/C;T | snv |
|
0.030 | 1.000 | 3 | 2014 | 2018 | |||||||||
|
1 | 247438293 | intron variant | T/C | snv | 0.58 |
|
0.800 | 1.000 | 3 | 2011 | 2019 | ||||||||||
|
0.689 | 0.560 | 1 | 247425556 | missense variant | C/A | snv | 3.9E-02 | 3.3E-02 |
|
0.030 | 0.667 | 3 | 2009 | 2016 | |||||||
|
1 | 247442297 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2013 | 2016 | |||||||||||
|
0.695 | 0.480 | 1 | 247448734 | 3 prime UTR variant | G/C;T | snv |
|
0.020 | 1.000 | 2 | 2010 | 2012 |