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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 |
|
0.840 | 1.000 | 1 | 2011 | 2019 | |||||||
|
0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 |
|
0.800 | 1.000 | 2 | 2010 | 2018 | |||||||
|
0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 |
|
0.800 | 1.000 | 2 | 2010 | 2018 | |||||||
|
0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||
|
0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 |
|
0.800 | 1.000 | 1 | 2009 | 2017 | |||||||
|
0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 |
|
0.800 | 1.000 | 1 | 2009 | 2016 | |||||||
|
0.882 | 0.120 | 6 | 26091108 | splice region variant | T/C | snv | 0.38 | 0.36 |
|
0.700 | 1.000 | 3 | 2010 | 2013 | |||||||
|
0.882 | 0.120 | 6 | 26091108 | splice region variant | T/C | snv | 0.38 | 0.36 |
|
0.700 | 1.000 | 3 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 6 | 26096818 | 3 prime UTR variant | T/C | snv | 0.76 |
|
0.700 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.925 | 0.120 | 6 | 26096818 | 3 prime UTR variant | T/C | snv | 0.76 |
|
0.700 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 |
|
0.800 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.882 | 0.160 | 6 | 26097156 | 3 prime UTR variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.882 | 0.160 | 6 | 26097156 | 3 prime UTR variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.827 | 0.200 | 6 | 26094139 | intron variant | G/A;T | snv | 0.52; 8.0E-06 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.827 | 0.200 | 6 | 26094139 | intron variant | G/A;T | snv | 0.52; 8.0E-06 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.120 | 6 | 26086235 | upstream gene variant | C/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.120 | 6 | 26086235 | upstream gene variant | C/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.120 | 6 | 26085789 | upstream gene variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.120 | 6 | 26085789 | upstream gene variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.120 | 6 | 26088662 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.120 | 6 | 26088662 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.120 | 6 | 26086974 | upstream gene variant | G/C | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.120 | 6 | 26086974 | upstream gene variant | G/C | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 |
|
0.800 | 1.000 | 2 | 2009 | 2012 |