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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 |
|
0.860 | 0.900 | 3 | 2005 | 2018 | |||||||
|
0.925 | 0.040 | 16 | 53605526 | missense variant | C/T | snv | 7.3E-02 | 4.7E-02 |
|
0.820 | 1.000 | 1 | 2013 | 2015 | |||||||
|
0.882 | 0.080 | 11 | 118827828 | intergenic variant | G/A | snv | 0.79 |
|
0.820 | 1.000 | 1 | 2013 | 2017 | ||||||||
|
0.851 | 0.040 | 6 | 31291060 | intron variant | G/A | snv | 0.44 |
|
0.820 | 1.000 | 1 | 2010 | 2012 | ||||||||
|
0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv |
|
0.810 | 1.000 | 3 | 2010 | 2015 | |||||||||
|
0.827 | 0.160 | 10 | 6056861 | intron variant | T/C | snv | 0.48 |
|
0.810 | 1.000 | 3 | 2010 | 2016 | ||||||||
|
0.925 | 0.040 | 14 | 24632954 | missense variant | C/T | snv | 0.76 | 0.72 |
|
0.810 | 1.000 | 2 | 2010 | 2018 | |||||||
|
0.882 | 0.120 | 12 | 56007301 | upstream gene variant | G/A | snv | 0.50 |
|
0.810 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.851 | 0.040 | 6 | 31869289 | intron variant | C/T | snv | 2.9E-02 | 4.5E-02 |
|
0.810 | 0.500 | 1 | 2010 | 2013 | |||||||
|
0.882 | 0.040 | 6 | 168540944 | intron variant | G/A;C | snv |
|
0.810 | 0.500 | 1 | 2010 | 2011 | |||||||||
|
0.925 | 0.040 | 10 | 71376162 | intron variant | G/A;C | snv |
|
0.810 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.040 | 12 | 56023144 | intron variant | A/C;G | snv |
|
0.810 | 1.000 | 1 | 2012 | 2015 | |||||||||
|
0.925 | 0.040 | 3 | 119569567 | intergenic variant | A/C;T | snv |
|
0.810 | 1.000 | 1 | 2012 | 2015 | |||||||||
|
0.882 | 0.040 | 6 | 32377506 | intron variant | C/A;T | snv | 4.2E-02 |
|
0.810 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.160 | 11 | 89277878 | intron variant | G/A | snv | 0.17 |
|
0.800 | 1.000 | 3 | 2010 | 2012 | ||||||||
|
0.925 | 0.160 | 22 | 37185445 | missense variant | C/A;G | snv | 0.43 |
|
0.800 | 1.000 | 3 | 2010 | 2016 | ||||||||
|
0.807 | 0.240 | 21 | 42416077 | intron variant | G/A | snv | 0.28 |
|
0.800 | 1.000 | 2 | 2010 | 2012 | ||||||||
|
0.827 | 0.280 | 6 | 32405921 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 2 | 2010 | 2012 | |||||||||
|
1.000 | 0.040 | 1 | 8466082 | intron variant | G/A | snv | 0.68 |
|
0.800 | 1.000 | 2 | 2010 | 2012 | ||||||||
|
1.000 | 0.040 | 11 | 35259305 | 3 prime UTR variant | A/G | snv | 0.33 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 11 | 95587644 | intron variant | T/C | snv | 0.14 |
|
0.800 | 1.000 | 1 | 2012 | 2016 | ||||||||
|
0.851 | 0.120 | 15 | 28111713 | 3 prime UTR variant | C/T | snv | 0.49 | 0.50 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.040 | 10 | 79256139 | intron variant | C/T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.040 | 3 | 188371466 | intron variant | C/T | snv | 0.44 |
|
0.800 | 1.000 | 1 | 2010 | 2016 | ||||||||
|
0.925 | 0.080 | 4 | 10725229 | intergenic variant | C/T | snv | 0.33 |
|
0.800 | 1.000 | 1 | 2012 | 2012 |