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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.120 | 2 | 27495607 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.120 | 2 | 27495607 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.120 | 2 | 27495607 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.120 | 2 | 27495607 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.120 | 2 | 27499104 | intron variant | T/C | snv | 0.42 | 0.47 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27499104 | intron variant | T/C | snv | 0.42 | 0.47 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27499104 | intron variant | T/C | snv | 0.42 | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.120 | 2 | 27499549 | intron variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||
|
0.925 | 0.120 | 2 | 27499549 | intron variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||
|
0.925 | 0.120 | 2 | 27505910 | intron variant | C/G | snv | 0.39 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||
|
0.925 | 0.120 | 2 | 27505910 | intron variant | C/G | snv | 0.39 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||
|
0.925 | 0.120 | 2 | 27505910 | intron variant | C/G | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.882 | 0.120 | 2 | 27506613 | non coding transcript exon variant | G/A | snv | 0.40 | 0.39 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.882 | 0.120 | 2 | 27506613 | non coding transcript exon variant | G/A | snv | 0.40 | 0.39 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 7 | 2008 | 2019 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 4 | 2010 | 2019 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 3 | 2010 | 2019 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 3 | 2010 | 2018 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 3 | 2010 | 2019 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 2 | 2011 | 2019 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.710 | 1.000 | 2 | 2010 | 2014 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.820 | 0.750 | 2 | 2010 | 2016 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 1 | 2009 | 2019 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 1 | 2009 | 2018 | |||||||
|
0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 |
|
0.800 | 1.000 | 1 | 2012 | 2019 |