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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.050 | 1.000 | 5 | 2013 | 2019 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.040 | 0.750 | 4 | 2013 | 2017 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.040 | 1.000 | 4 | 2011 | 2012 | ||||||||
|
0.925 | 0.080 | 7 | 150993088 | intron variant | C/T | snv | 5.7E-02 |
|
0.040 | 1.000 | 4 | 2012 | 2015 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.030 | 1.000 | 3 | 2016 | 2019 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.030 | 1.000 | 3 | 2014 | 2019 | ||||||||
|
0.763 | 0.320 | 7 | 150992855 | intron variant | G/A;C | snv |
|
0.020 | 1.000 | 2 | 2011 | 2014 | |||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.020 | 1.000 | 2 | 2015 | 2015 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.020 | 1.000 | 2 | 2008 | 2017 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.020 | 1.000 | 2 | 2018 | 2019 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.020 | 1.000 | 2 | 2014 | 2016 | ||||||||
|
0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 |
|
0.020 | 1.000 | 2 | 2012 | 2017 | ||||||||
|
0.925 | 0.120 | 7 | 151004695 | intron variant | G/A | snv | 0.35 |
|
0.020 | 0.500 | 2 | 2013 | 2014 | ||||||||
|
0.776 | 0.280 | 7 | 151005693 | intron variant | C/A;T | snv |
|
0.020 | < 0.001 | 2 | 2011 | 2011 | |||||||||
|
0.925 | 0.120 | 7 | 151009827 | intron variant | G/A;C | snv |
|
0.020 | 1.000 | 2 | 2011 | 2012 | |||||||||
|
0.790 | 0.200 | 7 | 150997269 | intron variant | GGGGGTGAGGAAGTCTAGACCTGCTGCG/A | delins |
|
0.020 | 1.000 | 2 | 2018 | 2019 | |||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | 7 | 151010603 | stop gained | C/T | snv | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2016 | 2016 |