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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.160 | X | 15572684 | intron variant | C/G | snv |
|
0.030 | 1.000 | 3 | 2018 | 2019 | |||||||||
|
0.925 | 0.080 | X | 15568841 | intron variant | C/T | snv |
|
0.020 | 1.000 | 2 | 2018 | 2019 | |||||||||
|
0.925 | 0.080 | X | 15558483 | downstream gene variant | C/G;T | snv |
|
0.020 | 1.000 | 2 | 2018 | 2019 | |||||||||
|
0.882 | 0.160 | X | 15572684 | intron variant | C/G | snv |
|
0.020 | 1.000 | 2 | 2018 | 2018 | |||||||||
|
1.000 | X | 15568325 | intron variant | A/G | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1.000 | X | 15568325 | intron variant | A/G | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1.000 | X | 15568325 | intron variant | A/G | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
X | 15599940 | intron variant | T/A;C | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
X | 15599940 | intron variant | T/A;C | snv |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1.000 | 0.040 | X | 15590376 | intron variant | T/G | snv |
|
0.010 | < 0.001 | 1 | 2018 | 2018 | |||||||||
|
X | 15564843 | intron variant | G/A | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.925 | 0.080 | X | 15568841 | intron variant | C/T | snv |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.925 | 0.080 | X | 15568841 | intron variant | C/T | snv |
|
0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.080 | X | 15568841 | intron variant | C/T | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
X | 15584941 | intron variant | G/A;C | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
X | 15578920 | intron variant | A/T | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||||||
|
X | 15578920 | intron variant | A/T | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.925 | 0.080 | X | 15558483 | downstream gene variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.925 | 0.080 | X | 15558483 | downstream gene variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.882 | 0.160 | X | 15572684 | intron variant | C/G | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.882 | 0.160 | X | 15572684 | intron variant | C/G | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.827 | 0.240 | X | 15578220 | missense variant | G/T | snv | 3.8E-05 | 9.5E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.827 | 0.240 | X | 15578220 | missense variant | G/T | snv | 3.8E-05 | 9.5E-06 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.827 | 0.240 | X | 15578220 | missense variant | G/T | snv | 3.8E-05 | 9.5E-06 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.827 | 0.240 | X | 15578220 | missense variant | G/T | snv | 3.8E-05 | 9.5E-06 |
|
0.010 | 1.000 | 1 | 2013 | 2013 |