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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.120 | 7 | 150951629 | missense variant | G/C;T | snv |
|
0.080 | 1.000 | 8 | 2005 | 2019 | |||||||||
|
0.925 | 0.120 | 7 | 150974931 | missense variant | G/T | snv |
|
0.030 | 1.000 | 3 | 1999 | 2015 | |||||||||
|
0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv |
|
0.830 | 1.000 | 3 | 1995 | 2017 | |||||||||
|
0.851 | 0.120 | 7 | 150952514 | missense variant | C/G;T | snv |
|
0.730 | 1.000 | 3 | 2001 | 2013 | |||||||||
|
1.000 | 0.040 | 7 | 150974126 | intron variant | C/A;T | snv |
|
0.030 | 1.000 | 3 | 2010 | 2019 | |||||||||
|
0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv |
|
0.820 | 1.000 | 2 | 1995 | 2019 | |||||||||
|
0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv |
|
0.020 | 1.000 | 2 | 2010 | 2017 | |||||||||
|
1.000 | 0.120 | 7 | 150959673 | missense variant | A/C;G | snv |
|
0.020 | 1.000 | 2 | 2004 | 2005 | |||||||||
|
1.000 | 0.080 | 7 | 150951540 | missense variant | G/A;C | snv |
|
0.020 | 1.000 | 2 | 2011 | 2019 | |||||||||
|
7 | 150947362 | missense variant | T/C | snv | 7.0E-06 |
|
0.020 | 1.000 | 2 | 2014 | 2018 | ||||||||||
|
1.000 | 0.120 | 7 | 150951475 | missense variant | A/C;G | snv |
|
0.720 | 1.000 | 2 | 1995 | 2009 | |||||||||
|
0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 |
|
0.020 | 1.000 | 2 | 2008 | 2012 | ||||||||
|
0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 |
|
0.020 | 1.000 | 2 | 2011 | 2017 | ||||||||
|
0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 |
|
0.020 | 1.000 | 2 | 2016 | 2017 | ||||||||
|
0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 |
|
0.020 | 1.000 | 2 | 2008 | 2010 | ||||||||
|
0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 |
|
0.020 | 1.000 | 2 | 2010 | 2017 | ||||||||
|
0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins |
|
0.020 | 1.000 | 2 | 2008 | 2010 | |||||||||
|
0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins |
|
0.020 | 1.000 | 2 | 2010 | 2017 | |||||||||
|
0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins |
|
0.020 | 1.000 | 2 | 2011 | 2017 | |||||||||
|
0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins |
|
0.020 | 1.000 | 2 | 2008 | 2012 | |||||||||
|
0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins |
|
0.020 | 1.000 | 2 | 2016 | 2017 | |||||||||
|
0.882 | 0.200 | 7 | 150951679 | missense variant | C/A;G;T | snv |
|
0.720 | 1.000 | 2 | 2000 | 2016 | |||||||||
|
0.851 | 0.120 | 7 | 150951629 | missense variant | G/C;T | snv |
|
0.010 | 1.000 | 1 | 2005 | 2005 | |||||||||
|
0.851 | 0.120 | 7 | 150951629 | missense variant | G/C;T | snv |
|
0.010 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
0.851 | 0.120 | 7 | 150951629 | missense variant | G/C;T | snv |
|
0.010 | 1.000 | 1 | 2005 | 2005 |