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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 |
|
0.820 | 1.000 | 1 | 2012 | 2016 | ||||||||
|
0.851 | 0.200 | 6 | 32082981 | intron variant | C/A;T | snv |
|
0.810 | 1.000 | 1 | 2011 | 2017 | |||||||||
|
1.000 | 0.040 | 6 | 32111790 | non coding transcript exon variant | T/C;G | snv |
|
0.810 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 6 | 32051969 | intron variant | G/C | snv | 0.25 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 6 | 32112369 | non coding transcript exon variant | A/C;G;T | snv |
|
0.710 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.925 | 0.120 | 6 | 32070923 | intron variant | C/T | snv | 0.25 |
|
0.700 | 1.000 | 3 | 2007 | 2011 | ||||||||
|
0.925 | 0.120 | 6 | 32062507 | intron variant | G/A | snv | 0.33 | 0.25 |
|
0.700 | 1.000 | 3 | 2007 | 2011 | |||||||
|
0.925 | 0.160 | 6 | 32115398 | 3 prime UTR variant | C/T | snv | 0.26 |
|
0.700 | 1.000 | 3 | 2007 | 2011 | ||||||||
|
0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.827 | 0.240 | 6 | 32059031 | intron variant | G/A | snv | 0.10 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
0.851 | 0.200 | 6 | 32082290 | missense variant | T/A;C;G | snv | 8.2E-06; 0.58; 4.1E-06 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.807 | 0.280 | 6 | 32108722 | intron variant | G/A | snv | 0.35 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
1.000 | 0.120 | 6 | 32061406 | missense variant | C/G;T | snv | 4.1E-06; 0.14 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.882 | 0.240 | 6 | 32104116 | intron variant | C/T | snv | 0.90 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.882 | 0.240 | 6 | 32096949 | missense variant | T/C;G | snv | 5.9E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 |