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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 |
|
0.100 | 0.826 | 23 | 2001 | 2019 | |||||||
|
0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv |
|
0.090 | 0.667 | 9 | 2001 | 2018 | |||||||||
|
0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 |
|
0.080 | 1.000 | 8 | 2006 | 2015 | |||||||
|
0.630 | 0.440 | 1 | 225838705 | missense variant | A/G;T | snv | 0.19; 2.8E-05 |
|
0.050 | 1.000 | 5 | 2006 | 2015 | ||||||||
|
0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 |
|
0.040 | 1.000 | 4 | 2007 | 2019 | |||||||
|
0.708 | 0.280 | 1 | 241878999 | missense variant | G/A | snv | 0.36 | 0.40 |
|
0.030 | 0.667 | 3 | 2008 | 2014 | |||||||
|
0.790 | 0.160 | 1 | 15524988 | intron variant | G/A;C | snv |
|
0.030 | 1.000 | 3 | 2010 | 2013 | |||||||||
|
0.559 | 0.760 | 1 | 226367601 | missense variant | A/G | snv | 0.21 | 0.15 |
|
0.020 | 1.000 | 2 | 2015 | 2019 | |||||||
|
0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 |
|
0.020 | 1.000 | 2 | 2010 | 2012 | |||||||
|
0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 |
|
0.020 | 1.000 | 2 | 2005 | 2011 | |||||||
|
0.576 | 0.600 | 1 | 186681189 | non coding transcript exon variant | C/G;T | snv |
|
0.020 | 1.000 | 2 | 2012 | 2015 | |||||||||
|
0.851 | 0.160 | 1 | 186676795 | intron variant | C/T | snv | 0.14 | 0.19 |
|
0.020 | 1.000 | 2 | 2010 | 2015 | |||||||
|
0.742 | 0.240 | 1 | 159711078 | downstream gene variant | C/T | snv | 0.77 |
|
0.020 | 1.000 | 2 | 2015 | 2016 | ||||||||
|
0.672 | 0.360 | 1 | 45331833 | missense variant | C/A;G | snv | 0.29 | 0.27 |
|
0.020 | 1.000 | 2 | 2004 | 2009 | |||||||
|
0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv |
|
0.020 | 1.000 | 2 | 2012 | 2018 | |||||||||
|
0.752 | 0.360 | 1 | 109688180 | missense variant | C/T | snv | 4.8E-04 |
|
0.020 | 1.000 | 2 | 2008 | 2017 | ||||||||
|
0.637 | 0.640 | 1 | 186681619 | upstream gene variant | T/C | snv | 0.17 |
|
0.020 | 1.000 | 2 | 2012 | 2018 | ||||||||
|
0.752 | 0.240 | 1 | 241889740 | 3 prime UTR variant | A/G | snv | 0.72 |
|
0.020 | 1.000 | 2 | 2008 | 2009 | ||||||||
|
0.851 | 0.080 | 1 | 40757742 | intron variant | G/A;T | snv | 0.50 |
|
0.020 | 0.500 | 2 | 2016 | 2018 | ||||||||
|
1.000 | 0.080 | 1 | 243199378 | intron variant | A/G | snv | 7.1E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.641 | 0.520 | 1 | 114713907 | missense variant | TT/CA;CC | mnv |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.701 | 0.280 | 1 | 155216951 | non coding transcript exon variant | G/A;T | snv | 0.46 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.851 | 0.080 | 1 | 45332251 | missense variant | A/G | snv |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 |
|
0.010 | 1.000 | 1 | 2012 | 2012 |