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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 |
|
0.900 | 1.000 | 4 | 2007 | 2019 | ||||||||
|
0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv |
|
0.840 | 1.000 | 3 | 2007 | 2012 | |||||||||
|
0.925 | 0.120 | 16 | 53776774 | intron variant | T/C | snv | 0.40 |
|
0.710 | 1.000 | 3 | 2007 | 2012 | ||||||||
|
0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 |
|
0.900 | 1.000 | 3 | 2007 | 2019 | ||||||||
|
0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 |
|
0.710 | 1.000 | 3 | 2007 | 2012 | ||||||||
|
0.716 | 0.560 | 16 | 53779455 | intron variant | T/A;G | snv |
|
0.890 | 1.000 | 2 | 2007 | 2016 | |||||||||
|
0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 |
|
0.800 | 0.947 | 2 | 2007 | 2020 | ||||||||
|
1.000 | 0.080 | 16 | 53766656 | intron variant | G/A | snv | 0.42 |
|
0.700 | 1.000 | 2 | 2007 | 2011 | ||||||||
|
0.851 | 0.120 | 8 | 11319901 | non coding transcript exon variant | G/A | snv | 0.35 |
|
0.720 | 1.000 | 1 | 2007 | 2014 | ||||||||
|
1.000 | 0.080 | 20 | 16988369 | intergenic variant | C/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.080 | 20 | 6048671 | intron variant | C/G | snv | 9.8E-02 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
1.000 | 0.080 | 18 | 60371593 | missense variant | C/T | snv | 5.6E-05 | 1.3E-04 |
|
0.810 | 1.000 | 0 | 2007 | 2007 | |||||||
|
0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 |
|
0.820 | 0.833 | 4 | 2008 | 2013 | ||||||||
|
0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 |
|
0.900 | 0.905 | 1 | 2008 | 2019 | ||||||||
|
0.776 | 0.360 | 16 | 53796553 | intron variant | A/G | snv | 0.36 |
|
0.760 | 0.857 | 1 | 2008 | 2018 | ||||||||
|
1.000 | 0.080 | 16 | 53791576 | intron variant | C/T | snv | 0.34 |
|
0.810 | 1.000 | 3 | 2009 | 2017 | ||||||||
|
1.000 | 0.080 | 10 | 16257952 | intergenic variant | C/A;T | snv |
|
0.810 | 1.000 | 1 | 2009 | 2013 | |||||||||
|
1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 |
|
0.720 | 0.667 | 1 | 2009 | 2013 | ||||||||
|
1.000 | 0.080 | 16 | 79648854 | regulatory region variant | T/C | snv | 0.44 |
|
0.810 | 1.000 | 1 | 2009 | 2013 | ||||||||
|
0.925 | 0.120 | 18 | 23560468 | missense variant | T/C | snv | 0.33 | 0.29 |
|
0.830 | 1.000 | 1 | 2009 | 2013 | |||||||
|
1.000 | 0.080 | 1 | 219470882 | intergenic variant | A/G | snv | 0.77 |
|
0.710 | 1.000 | 1 | 2009 | 2011 | ||||||||
|
0.925 | 0.120 | 11 | 16368048 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
1.000 | 0.080 | 6 | 22078386 | intron variant | G/A | snv | 0.64 |
|
0.720 | 1.000 | 1 | 2009 | 2013 | ||||||||
|
0.925 | 0.120 | 11 | 16381965 | intron variant | T/C | snv | 8.8E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.080 | 2 | 638144 | regulatory region variant | G/T | snv | 0.82 |
|
0.730 | 1.000 | 1 | 2009 | 2018 |