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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 0.827 | 0.200 | 1 | 156137666 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 14 | 2003 | 2017 | |||||
|
1 | 1.000 | 0.080 | 1 | 156134909 | missense variant | GC/TT | mnv | 0.700 | 1.000 | 11 | 2000 | 2015 | |||||
|
11 | 0.776 | 0.200 | 1 | 156136094 | missense variant | G/A;T | snv | 0.700 | 1.000 | 11 | 2000 | 2016 | |||||
|
2 | 0.925 | 0.120 | 1 | 156136422 | missense variant | A/G;T | snv | 0.700 | 1.000 | 10 | 2000 | 2015 | |||||
|
8 | 0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 | 0.700 | 1.000 | 10 | 1999 | 2015 | ||||
|
6 | 0.807 | 0.280 | 1 | 156136009 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 9 | 2004 | 2017 | ||||
|
3 | 0.925 | 0.120 | 1 | 156136093 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 9 | 2003 | 2014 | ||||
|
7 | 0.827 | 0.280 | 1 | 156138613 | splice region variant | C/A;T | snv | 8.1E-06 | 0.700 | 1.000 | 9 | 2003 | 2017 | ||||
|
3 | 0.882 | 0.120 | 1 | 156134910 | missense variant | C/G;T | snv | 0.700 | 1.000 | 8 | 2008 | 2015 | |||||
|
7 | 0.827 | 0.160 | 1 | 156134457 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 8 | 2002 | 2015 | ||||
|
5 | 0.827 | 0.120 | 1 | 156136036 | stop gained | G/A;T | snv | 0.700 | 1.000 | 8 | 2000 | 2014 | |||||
|
4 | 0.882 | 0.160 | 1 | 156134458 | missense variant | G/A;T | snv | 0.700 | 1.000 | 7 | 2002 | 2017 | |||||
|
2 | 0.925 | 0.120 | 1 | 156115010 | inframe deletion | AAG/- | delins | 0.700 | 1.000 | 7 | 2002 | 2014 | |||||
|
5 | 0.851 | 0.160 | 1 | 156137667 | missense variant | G/A;C | snv | 0.700 | 1.000 | 7 | 2000 | 2017 | |||||
|
6 | 0.827 | 0.160 | 1 | 156134496 | missense variant | G/A | snv | 0.700 | 1.000 | 6 | 1999 | 2012 | |||||
|
7 | 0.807 | 0.240 | 1 | 156136359 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 0.700 | 1.000 | 5 | 2003 | 2014 | |||
|
3 | 0.925 | 0.120 | 1 | 156136952 | missense variant | G/A;C | snv | 1.4E-05 | 0.700 | 1.000 | 5 | 2007 | 2017 | ||||
|
2 | 1.000 | 0.080 | 1 | 156137233 | splice donor variant | G/A | snv | 0.700 | 1.000 | 5 | 2005 | 2014 | |||||
|
4 | 0.882 | 0.160 | 1 | 156134474 | missense variant | C/A;G | snv | 0.700 | 1.000 | 5 | 2001 | 2013 | |||||
|
3 | 1.000 | 0.080 | 1 | 156137144 | frameshift variant | -/C | delins | 0.700 | 1.000 | 5 | 2011 | 2017 | |||||
|
8 | 0.776 | 0.200 | 1 | 156136413 | missense variant | C/T | snv | 0.700 | 1.000 | 5 | 1991 | 2011 | |||||
|
5 | 0.827 | 0.160 | 1 | 156134911 | missense variant | G/A | snv | 0.700 | 1.000 | 5 | 2000 | 2014 | |||||
|
11 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 5 | 1990 | 2014 | ||||
|
7 | 0.790 | 0.280 | 1 | 156130658 | missense variant | G/A;C;T | snv | 4.0E-06 | 0.700 | 1.000 | 5 | 2001 | 2005 | ||||
|
2 | 1.000 | 0.080 | 1 | 156134811 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 0.700 | 1.000 | 5 | 2013 | 2018 |