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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.100 | 0.885 | 26 | 1994 | 2019 | |||||||
|
0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 |
|
0.100 | 0.929 | 14 | 2005 | 2017 | |||||||
|
0.790 | 0.160 | 11 | 113475529 | intron variant | -/G | delins |
|
0.050 | 1.000 | 5 | 2007 | 2019 | |||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.040 | 1.000 | 4 | 2012 | 2017 | ||||||||
|
0.851 | 0.160 | 11 | 113412755 | synonymous variant | A/G | snv | 0.64 | 0.58 |
|
0.040 | 0.750 | 4 | 2008 | 2016 | |||||||
|
0.851 | 0.160 | 11 | 113412755 | synonymous variant | A/G | snv | 0.64 | 0.58 |
|
0.040 | 0.750 | 4 | 2012 | 2015 | |||||||
|
0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 |
|
0.040 | 1.000 | 4 | 2008 | 2012 | |||||||
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.030 | 1.000 | 3 | 2001 | 2005 | |||||||
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.030 | 0.667 | 3 | 1996 | 1998 | |||||||
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.030 | 1.000 | 3 | 2001 | 2005 | |||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2007 | 2014 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2011 | 2014 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 0.500 | 2 | 2015 | 2019 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2016 | 2018 | ||||||||
|
0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 |
|
0.020 | 0.500 | 2 | 2015 | 2019 | ||||||||
|
0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 |
|
0.020 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 |
|
0.020 | 1.000 | 2 | 2014 | 2017 | ||||||||
|
1.000 | 0.040 | 11 | 113418460 | intron variant | T/C | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2013 | 2014 | ||||||||
|
0.790 | 0.160 | 11 | 113475529 | intron variant | -/G | delins |
|
0.020 | 0.500 | 2 | 2013 | 2015 | |||||||||
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.020 | 1.000 | 2 | 1996 | 2000 | |||||||
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.020 | 1.000 | 2 | 1996 | 2010 | |||||||
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.020 | 0.500 | 2 | 1998 | 2000 | |||||||
|
0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 |
|
0.020 | 1.000 | 2 | 1995 | 2003 | |||||||
|
0.776 | 0.160 | 11 | 113414814 | intron variant | C/A | snv | 0.16 |
|
0.020 | 1.000 | 2 | 2013 | 2014 | ||||||||
|
0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 |
|
0.020 | 0.500 | 2 | 2008 | 2013 |