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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
93 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.120 | 8 | 117799852 | stop gained | G/A | snv | 4.0E-06 | 0.700 | 1.000 | 2 | 2001 | 2015 | ||||
|
1 | 1.000 | 0.120 | 8 | 117799849 | stop gained | G/A | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
1 | 1.000 | 0.120 | 8 | 117807290 | stop gained | C/A | snv | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||
|
1 | 1.000 | 0.120 | 8 | 118110195 | stop gained | A/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 117835543 | stop gained | G/A;T | snv | 0.26 | 0.24 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 8 | 118110768 | stop gained | G/A;C | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 8 | 117818491 | stop gained | T/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 117822544 | stop gained | -/TCCATATTAAACTGTTACGTGAT | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 117822566 | stop gained | G/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 117837145 | missense variant | C/A;T | snv | 4.0E-06 | 0.700 | 1.000 | 12 | 1997 | 2016 | ||||
|
1 | 1.000 | 0.120 | 8 | 117837146 | missense variant | G/A | snv | 0.700 | 1.000 | 12 | 1997 | 2016 | |||||
|
1 | 1.000 | 0.120 | 8 | 118110209 | missense variant | T/C | snv | 0.800 | 1.000 | 8 | 1997 | 2001 | |||||
|
1 | 1.000 | 0.120 | 8 | 117837148 | missense variant | C/T | snv | 0.700 | 1.000 | 4 | 1997 | 2013 | |||||
|
1 | 1.000 | 0.120 | 8 | 117837128 | missense variant | T/C | snv | 0.700 | 1.000 | 3 | 2007 | 2014 | |||||
|
1 | 1.000 | 0.120 | 8 | 118110207 | missense variant | C/G | snv | 0.700 | 1.000 | 1 | 1998 | 1998 | |||||
|
1 | 1.000 | 0.120 | 8 | 118110475 | missense variant | A/G | snv | 0.700 | 1.000 | 1 | 2006 | 2006 | |||||
|
2 | 0.925 | 0.120 | 8 | 117799833 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 1.000 | 0.120 | 8 | 117837143 | missense variant | T/A;C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 117837172 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 8 | 117819755 | missense variant | G/A | snv | 2.5E-04 | 7.7E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 8 | 117837107 | splice donor variant | C/A;T | snv | 0.700 | 1.000 | 8 | 1991 | 2009 | |||||
|
1 | 1.000 | 0.120 | 8 | 117822463 | splice donor variant | A/T | snv | 0.700 | 1.000 | 4 | 2000 | 2009 | |||||
|
1 | 1.000 | 0.120 | 8 | 117837107 | splice donor variant | CCTGC/- | del | 0.700 | 1.000 | 3 | 2000 | 2009 | |||||
|
1 | 1.000 | 0.120 | 8 | 117837106 | splice donor variant | A/T | snv | 0.700 | 0 |