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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.807 | 0.080 | 12 | 120994405 | missense variant | G/A | snv | 1.4E-05 |
|
0.800 | 0.917 | 12 | 2000 | 2011 | ||||||||
|
1.000 | 0.080 | 11 | 2670241 | non coding transcript exon variant | A/G | snv | 0.62 |
|
0.840 | 1.000 | 10 | 2010 | 2019 | ||||||||
|
1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 |
|
0.820 | 1.000 | 10 | 2008 | 2019 | ||||||||
|
0.851 | 0.080 | 11 | 17396930 | missense variant | C/A;T | snv | 0.64; 8.0E-06 |
|
0.790 | 0.900 | 10 | 1997 | 2018 | ||||||||
|
0.882 | 0.080 | 20 | 44351879 | non coding transcript exon variant | C/T | snv | 0.18 |
|
0.090 | 0.889 | 9 | 2004 | 2016 | ||||||||
|
0.925 | 0.080 | 3 | 23294959 | intron variant | C/A;G | snv |
|
0.840 | 0.889 | 9 | 2010 | 2018 | |||||||||
|
0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 |
|
0.840 | 0.875 | 8 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 11 | 72722053 | 5 prime UTR variant | A/C | snv | 0.12 |
|
0.820 | 1.000 | 8 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 11 | 2825839 | intron variant | T/G | snv | 0.40 |
|
0.810 | 1.000 | 8 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 11 | 2828300 | intron variant | A/C | snv | 0.10 |
|
0.760 | 1.000 | 8 | 2009 | 2017 | ||||||||
|
0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 |
|
0.830 | 1.000 | 8 | 2010 | 2019 | ||||||||
|
1.000 | 0.080 | 7 | 130782095 | intergenic variant | A/G;T | snv |
|
0.840 | 1.000 | 8 | 2010 | 2016 | |||||||||
|
1.000 | 0.080 | 6 | 20687890 | intron variant | T/A;G | snv | 0.26 |
|
0.820 | 1.000 | 7 | 2010 | 2019 | ||||||||
|
1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 |
|
0.800 | 1.000 | 7 | 2013 | 2019 | ||||||||
|
0.882 | 0.080 | 12 | 120979061 | missense variant | C/T | snv | 2.9E-02 | 2.2E-02 |
|
0.850 | 0.857 | 7 | 2004 | 2018 | |||||||
|
0.925 | 0.080 | 20 | 44414511 | missense variant | C/T | snv |
|
0.070 | 1.000 | 7 | 2003 | 2017 | |||||||||
|
1.000 | 0.080 | 13 | 80143021 | intergenic variant | G/A | snv | 0.23 |
|
0.810 | 1.000 | 6 | 2010 | 2019 | ||||||||
|
0.882 | 0.080 | 13 | 27920364 | missense variant | G/A;T | snv | 2.9E-03 |
|
0.760 | 0.833 | 6 | 2000 | 2015 | ||||||||
|
1.000 | 0.080 | 11 | 2800385 | intron variant | A/C | snv | 0.67 |
|
0.060 | 0.833 | 6 | 2009 | 2019 | ||||||||
|
0.882 | 0.080 | 7 | 127613496 | missense variant | C/T | snv | 8.2E-03 | 2.1E-03 |
|
0.740 | 0.833 | 6 | 2013 | 2019 | |||||||
|
1.000 | 0.080 | 11 | 2837210 | intron variant | G/A;T | snv |
|
0.810 | 1.000 | 6 | 2011 | 2019 | |||||||||
|
1.000 | 0.080 | 2 | 60357684 | intron variant | G/A | snv | 0.45 |
|
0.820 | 1.000 | 6 | 2010 | 2017 | ||||||||
|
0.925 | 0.080 | 2 | 10046292 | missense variant | A/G;T | snv | 9.3E-02 |
|
0.060 | 0.833 | 6 | 2005 | 2009 | ||||||||
|
1.000 | 0.080 | 8 | 41661730 | non coding transcript exon variant | T/A;C | snv | 0.78 |
|
0.820 | 1.000 | 6 | 2012 | 2018 | ||||||||
|
1.000 | 0.080 | 9 | 4289050 | intron variant | C/A;G | snv |
|
0.750 | 1.000 | 6 | 2011 | 2019 |