| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 1 | 2011 | 2019 | |||||||||
|
1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
8 | 100944649 | intron variant | C/T | snv | 4.0E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
2 | 10135619 | intron variant | A/C | snv | 0.59 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
2 | 10151287 | intron variant | G/C | snv | 0.65 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
2 | 10153562 | intron variant | C/T | snv | 0.64 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
2 | 10156359 | intron variant | T/C | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
4 | 101639133 | intron variant | A/C | snv | 8.6E-02 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.120 | 10 | 102836092 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 2 | 2011 | 2013 | |||||||||
|
10 | 102869254 | intron variant | T/C | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
8 | 10295771 | intron variant | T/C | snv | 0.73 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
0.882 | 0.080 | 10 | 103086421 | 3 prime UTR variant | T/C | snv | 8.6E-02 |
|
0.700 | 1.000 | 3 | 2011 | 2011 | ||||||||
|
11 | 10310742 | intron variant | G/T | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
10 | 103179458 | intron variant | T/C | snv | 9.0E-02 |
|
0.700 | 1.000 | 2 | 2011 | 2013 | ||||||||||
|
11 | 10328991 | intron variant | G/A | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
5 | 104843088 | intron variant | G/A | snv | 9.0E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
1.000 | 0.080 | 7 | 106771412 | upstream gene variant | T/C | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 1 | 10736809 | intron variant | T/C | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
2 | 108267586 | downstream gene variant | G/A | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
13 | 108695311 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
20 | 10988382 | intron variant | A/G | snv | 0.46 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
4 | 110460482 | intron variant | C/T | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 |
|
0.700 | 1.000 | 1 | 2011 | 2011 |