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 | 0.040 | 7 | 55091656 | intron variant | A/G;T | snv | 0.20 |
|
0.850 | 1.000 | 6 | 2011 | 2018 | ||||||||
|
0.570 | 0.560 | 7 | 55191821 | missense variant | CT/AG | mnv |
|
0.800 | 0.983 | 176 | 2004 | 2020 | |||||||||
|
0.570 | 0.560 | 7 | 55191822 | missense variant | TG/GT | mnv |
|
0.800 | 0.983 | 176 | 2004 | 2020 | |||||||||
|
0.568 | 0.560 | 7 | 55191822 | missense variant | T/A;G | snv |
|
0.800 | 0.983 | 176 | 2004 | 2020 | |||||||||
|
1.000 | 7 | 55157738 | missense variant | G/A | snv | 4.0E-06 |
|
0.800 | 0 | ||||||||||||
|
0.807 | 0.120 | 7 | 55174014 | missense variant | G/A;C;T | snv |
|
0.750 | 1.000 | 21 | 2004 | 2019 | |||||||||
|
0.724 | 0.160 | 7 | 55191831 | missense variant | T/A;C;G | snv |
|
0.750 | 1.000 | 11 | 2004 | 2020 | |||||||||
|
0.827 | 0.120 | 7 | 55174015 | missense variant | G/A;C | snv |
|
0.740 | 1.000 | 21 | 1990 | 2019 | |||||||||
|
0.763 | 0.160 | 7 | 55181312 | missense variant | G/T | snv |
|
0.740 | 1.000 | 11 | 2004 | 2018 | |||||||||
|
0.790 | 0.120 | 7 | 55181312 | missense variant | GC/TT | mnv |
|
0.740 | 1.000 | 10 | 2004 | 2018 | |||||||||
|
0.807 | 0.120 | 7 | 55174014 | missense variant | G/A;C;T | snv |
|
0.720 | 1.000 | 3 | 2016 | 2018 | |||||||||
|
0.724 | 0.160 | 7 | 55191831 | missense variant | T/A;C;G | snv |
|
0.710 | 1.000 | 2 | 2016 | 2020 | |||||||||
|
0.807 | 0.080 | 7 | 55154129 | missense variant | C/A;T | snv |
|
0.710 | 1.000 | 2 | 2016 | 2018 | |||||||||
|
0.882 | 0.160 | 7 | 55174818 | missense variant | G/A;T | snv |
|
0.700 | 1.000 | 5 | 2006 | 2014 | |||||||||
|
1.000 | 0.040 | 7 | 55174771 | missense variant | A/G | snv |
|
0.700 | 1.000 | 3 | 2010 | 2014 | |||||||||
|
0.724 | 0.160 | 7 | 55191831 | missense variant | T/A;C;G | snv |
|
0.700 | 1.000 | 3 | 2012 | 2016 | |||||||||
|
1.000 | 0.080 | 7 | 55181320 | protein altering variant | -/ACC | delins |
|
0.700 | 1.000 | 3 | 2005 | 2011 | |||||||||
|
0.925 | 0.080 | 7 | 55174785 | missense variant | G/C | snv | 4.0E-06 |
|
0.700 | 1.000 | 2 | 2005 | 2014 | ||||||||
|
0.925 | 0.080 | 7 | 55174785 | missense variant | G/C | snv | 4.0E-06 |
|
0.700 | 1.000 | 2 | 2012 | 2014 | ||||||||
|
1.000 | 0.080 | 7 | 55174794 | missense variant | C/T | snv | 8.0E-06 |
|
0.700 | 1.000 | 2 | 2007 | 2014 | ||||||||
|
1.000 | 0.080 | 7 | 55174737 | missense variant | G/A | snv |
|
0.700 | 1.000 | 2 | 2010 | 2014 | |||||||||
|
0.827 | 0.120 | 7 | 55174015 | missense variant | G/A;C | snv |
|
0.700 | 1.000 | 2 | 2012 | 2013 | |||||||||
|
1.000 | 0.080 | 7 | 55174740 | missense variant | G/A | snv |
|
0.700 | 1.000 | 2 | 2013 | 2014 | |||||||||
|
1.000 | 0.080 | 7 | 55181327 | missense variant | A/G | snv |
|
0.700 | 1.000 | 2 | 2008 | 2014 | |||||||||
|
0.925 | 0.120 | 7 | 55174735 | missense variant | C/T | snv |
|
0.700 | 1.000 | 2 | 2013 | 2014 |