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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 0.882 | 0.120 | 17 | 50196670 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.240 | 17 | 50196163 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50195433 | splice donor variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 17 | 50192807 | frameshift variant | GGGG/-;GGG | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 17 | 50191454 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 17 | 50188765 | stop gained | G/A;C | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 17 | 50187486 | stop gained | G/A;T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 17 | 50198170 | frameshift variant | A/- | del | 0.700 | 0 | ||||||||
|
5 | 0.827 | 0.160 | 17 | 50194032 | missense variant | C/A;G;T | snv | 0.710 | 1.000 | 1 | 2001 | 2001 | |||||
|
2 | 0.925 | 0.120 | 17 | 50195227 | splice region variant | C/T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.120 | 17 | 50187885 | frameshift variant | A/- | del | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
2 | 0.925 | 0.120 | 17 | 50195469 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 2002 | 2002 | |||||
|
2 | 0.925 | 0.120 | 17 | 50195967 | missense variant | C/A;T | snv | 7.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 0.925 | 0.120 | 17 | 50188776 | missense variant | C/A;G;T | snv | 0.010 | 1.000 | 1 | 1992 | 1992 | |||||
|
2 | 0.925 | 0.120 | 17 | 50197205 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 1995 | 1995 | |||||
|
3 | 0.882 | 0.200 | 17 | 50197057 | stop gained | G/A | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
|
5 | 0.827 | 0.200 | 17 | 50190861 | missense variant | C/T | snv | 7.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.882 | 0.200 | 17 | 50188541 | missense variant | G/A;C | snv | 6.4E-05 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
2 | 0.925 | 0.120 | 17 | 50186799 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
|
3 | 0.882 | 0.120 | 17 | 50186386 | stop gained | C/A;T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
2 | 1.000 | 0.120 | 17 | 50185576 | missense variant | C/A;T | snv | 2.8E-05 | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||
|
2 | 0.925 | 0.200 | 17 | 50189478 | missense variant | G/A | snv | 4.0E-06 | 2.8E-05 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||
|
2 | 0.925 | 0.120 | 17 | 50187041 | missense variant | C/A;T | snv | 0.700 | 1.000 | 2 | 2007 | 2016 | |||||
|
3 | 0.882 | 0.120 | 17 | 50188122 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2011 | 2012 |