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 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2009 | 2019 | ||||||||
|
1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 |
|
0.700 | 1.000 | 14 | 2010 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
1.000 | 0.080 | 18 | 60161902 | upstream gene variant | T/C | snv | 0.21 |
|
0.700 | 1.000 | 12 | 2014 | 2019 | ||||||||
|
0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv |
|
0.700 | 1.000 | 12 | 2009 | 2019 | |||||||||
|
0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 |
|
0.700 | 1.000 | 11 | 2010 | 2019 | ||||||||
|
0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 |
|
0.700 | 1.000 | 11 | 2010 | 2019 | ||||||||
|
13 | 53528071 | intron variant | G/A;T | snv | 0.12 |
|
0.700 | 1.000 | 10 | 2015 | 2019 | ||||||||||
|
0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 |
|
0.700 | 1.000 | 10 | 2009 | 2019 | ||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 10 | 2010 | 2019 | ||||||||||
|
0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 |
|
0.700 | 1.000 | 9 | 2011 | 2019 | ||||||||
|
0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 |
|
0.700 | 1.000 | 9 | 2011 | 2019 | ||||||||
|
0.925 | 0.120 | 5 | 75719417 | upstream gene variant | T/G | snv | 0.42 |
|
0.700 | 1.000 | 9 | 2010 | 2019 | ||||||||
|
0.925 | 0.120 | 1 | 10736809 | intron variant | T/C | snv | 0.32 |
|
0.700 | 1.000 | 9 | 2011 | 2018 | ||||||||
|
0.882 | 0.200 | 17 | 61379228 | non coding transcript exon variant | C/T | snv | 0.69 |
|
0.700 | 1.000 | 9 | 2016 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 24927427 | intergenic variant | A/G | snv | 0.57 |
|
0.700 | 1.000 | 8 | 2015 | 2019 | ||||||||
|
0.882 | 0.080 | 10 | 103086421 | 3 prime UTR variant | T/C | snv | 8.6E-02 |
|
0.700 | 1.000 | 8 | 2009 | 2018 | ||||||||
|
2 | 632348 | intergenic variant | A/G | snv | 0.85 |
|
0.700 | 1.000 | 8 | 2015 | 2019 | ||||||||||
|
0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 |
|
0.700 | 1.000 | 8 | 2011 | 2019 | ||||||||
|
0.882 | 0.120 | 12 | 89666809 | intron variant | G/A | snv | 0.15 |
|
0.700 | 1.000 | 8 | 2009 | 2018 |