Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.925 | 0.080 | 12 | 120988982 | missense variant | G/A | snv | 0.700 | 1.000 | 5 | 1997 | 2010 | |||||
|
2 | 0.925 | 0.080 | 12 | 120996261 | splice acceptor variant | G/A;C | snv | 0.700 | 1.000 | 3 | 2009 | 2013 | |||||
|
2 | 0.925 | 0.080 | 12 | 120993532 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
4 | 0.882 | 0.080 | 12 | 120999288 | missense variant | G/A;C | snv | 4.9E-04 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.080 | 12 | 120997666 | splice donor variant | G/A | snv | 0.700 | 0 | ||||||||
|
6 | 0.807 | 0.280 | 12 | 120997504 | missense variant | C/T | snv | 1.2E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 12 | 120988871 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 121001155 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 12 | 120988841 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.200 | 12 | 120988897 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 120994277 | missense variant | C/A;G | snv | 8.0E-06; 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 12 | 120999358 | missense variant | G/C | snv | 2.0E-05 | 0.700 | 0 | |||||||
|
5 | 0.851 | 0.200 | 12 | 120978860 | missense variant | G/A;C | snv | 7.7E-04; 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 12 | 120994163 | splice acceptor variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 120988973 | missense variant | C/A;T | snv | 1.2E-05; 6.4E-05 | 0.700 | 0 | |||||||
|
6 | 0.807 | 0.280 | 12 | 120994264 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 120996698 | missense variant | T/C | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 12 | 120997588 | missense variant | C/A;T | snv | 1.2E-05; 5.2E-05 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.160 | 12 | 120999522 | missense variant | C/T | snv | 8.1E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 12 | 120999604 | missense variant | A/G | snv | 5.4E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 12 | 120978769 | start lost | A/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 120979049 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 120988947 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 120993591 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 12 | 120993663 | missense variant | C/T | snv | 0.700 | 0 |