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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.763 | 0.280 | 11 | 102530930 | upstream gene variant | T/A;C | snv |
|
0.720 | 0.667 | 1 | 2013 | 2018 | |||||||||
|
0.925 | 0.080 | 10 | 102654464 | non coding transcript exon variant | A/G | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 |
|
0.720 | 0.667 | 1 | 2009 | 2014 | ||||||||
|
0.925 | 0.080 | 9 | 107394019 | intergenic variant | C/T | snv | 0.81 |
|
0.710 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.080 | 6 | 108963986 | intron variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 110279296 | splice donor variant | T/C | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 10 | 110280017 | missense variant | A/C | snv |
|
0.800 | 1.000 | 5 | 2008 | 2015 | |||||||||
|
1.000 | 0.080 | 6 | 113055846 | intron variant | A/G | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.925 | 0.080 | 3 | 113556777 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.080 | 12 | 114247766 | intergenic variant | A/G | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 4 | 116449550 | intergenic variant | C/T | snv | 2.0E-03 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 3 | 116668062 | intron variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 3 | 116671823 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.882 | 0.080 | 6 | 116888889 | intron variant | T/C | snv | 0.28 |
|
0.760 | 0.857 | 1 | 2010 | 2016 | ||||||||
|
1.000 | 0.080 | 7 | 118064652 | intergenic variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.925 | 0.080 | 10 | 121273005 | intergenic variant | G/A | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.160 | 10 | 125008303 | intron variant | T/C | snv | 0.23 |
|
0.720 | 1.000 | 1 | 2008 | 2016 | ||||||||
|
1.000 | 0.080 | 7 | 125296388 | intron variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 7 | 125304928 | intron variant | G/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 8 | 126912414 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.807 | 0.240 | 8 | 127081052 | non coding transcript exon variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 4 | 2008 | 2013 | ||||||||
|
0.827 | 0.160 | 8 | 127082911 | non coding transcript exon variant | A/G | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.790 | 0.200 | 8 | 127091692 | non coding transcript exon variant | T/A;C | snv |
|
0.720 | 1.000 | 4 | 2010 | 2014 | |||||||||
|
0.807 | 0.160 | 8 | 127092098 | non coding transcript exon variant | C/A;T | snv |
|
0.720 | 0.667 | 1 | 2008 | 2012 | |||||||||
|
0.925 | 0.080 | 8 | 127094635 | intron variant | A/C | snv | 0.17 |
|
0.780 | 1.000 | 1 | 2008 | 2017 |