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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.160 | 6 | 34242693 | intron variant | -/C | delins |
|
0.040 | 1.000 | 4 | 2013 | 2017 | |||||||||
|
0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins |
|
0.020 | 1.000 | 2 | 2008 | 2011 | |||||||||
|
0.925 | 0.160 | 2 | 240594824 | intron variant | -/CGGGAGGAGGGTGATGATTCTGTCCCAGGAGC | delins |
|
0.720 | 1.000 | 2 | 2010 | 2011 | |||||||||
|
0.925 | 0.160 | 3 | 185811292 | intron variant | A/C | snv | 0.46 |
|
0.900 | 0.963 | 16 | 2007 | 2017 | ||||||||
|
0.827 | 0.160 | 6 | 20660803 | intron variant | A/C | snv | 0.40 |
|
0.900 | 1.000 | 10 | 2007 | 2019 | ||||||||
|
1.000 | 0.080 | 11 | 2800385 | intron variant | A/C | snv | 0.67 |
|
0.060 | 0.833 | 6 | 2009 | 2019 | ||||||||
|
1.000 | 0.080 | 11 | 2828300 | intron variant | A/C | snv | 0.10 |
|
0.760 | 1.000 | 6 | 2009 | 2017 | ||||||||
|
0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 |
|
0.030 | 0.667 | 3 | 2008 | 2013 | |||||||
|
0.882 | 0.200 | 1 | 42935767 | intron variant | A/C | snv | 0.66 |
|
0.030 | 1.000 | 3 | 2013 | 2019 | ||||||||
|
1.000 | 0.080 | 3 | 186620636 | synonymous variant | A/C | snv | 0.76 | 0.77 |
|
0.020 | 1.000 | 2 | 2005 | 2009 | |||||||
|
1.000 | 0.080 | 11 | 45851540 | intron variant | A/C | snv | 0.39 |
|
0.020 | 1.000 | 2 | 2011 | 2012 | ||||||||
|
1.000 | 0.080 | 3 | 186854691 | missense variant | A/C | snv | 3.9E-04 | 1.8E-04 |
|
0.020 | < 0.001 | 2 | 2010 | 2014 | |||||||
|
1.000 | 0.080 | 11 | 72722053 | 5 prime UTR variant | A/C | snv | 0.12 |
|
0.820 | 1.000 | 2 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 4 | 74794307 | missense variant | A/C | snv | 0.19 | 0.25 |
|
0.020 | 1.000 | 2 | 2005 | 2006 | |||||||
|
0.776 | 0.320 | 8 | 118952749 | upstream gene variant | A/C | snv | 9.6E-02 |
|
0.020 | 1.000 | 2 | 2013 | 2015 | ||||||||
|
0.790 | 0.360 | 6 | 160249250 | missense variant | A/C | snv | 0.90 | 0.89 |
|
0.020 | 1.000 | 2 | 2010 | 2015 | |||||||
|
0.925 | 0.120 | 4 | 23961283 | intergenic variant | A/C | snv | 6.9E-02 |
|
0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.160 | 10 | 103927874 | intergenic variant | A/C | snv | 0.16 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.708 | 0.240 | 11 | 113932306 | missense variant | A/C | snv | 0.33 | 0.36 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.120 | 8 | 19951825 | missense variant | A/C | snv | 4.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 1993 | 1993 | |||||||
|
0.851 | 0.240 | 4 | 94593458 | intron variant | A/C | snv | 0.54 |
|
0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.925 | 0.160 | 5 | 53048731 | missense variant | A/C | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.925 | 0.120 | 18 | 13825728 | splice region variant | A/C | snv | 0.17 | 0.19 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
1.000 | 0.080 | 2 | 168913876 | upstream gene variant | A/C | snv | 6.0E-02 |
|
0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.851 | 0.200 | 17 | 42552898 | 5 prime UTR variant | A/C | snv | 7.8E-03 | 8.2E-03 |
|
0.010 | 1.000 | 1 | 2015 | 2015 |