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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins |
|
0.030 | 1.000 | 3 | 2009 | 2016 | |||||||||
|
0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins |
|
0.030 | 1.000 | 3 | 2016 | 2018 | |||||||||
|
0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins |
|
0.020 | 1.000 | 2 | 2010 | 2016 | |||||||||
|
0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins |
|
0.020 | 1.000 | 2 | 2007 | 2009 | |||||||||
|
0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins |
|
0.020 | 1.000 | 2 | 2009 | 2016 | |||||||||
|
0.724 | 0.400 | 17 | 63476833 | upstream gene variant | T/A;C | snv |
|
0.020 | 1.000 | 2 | 2008 | 2009 | |||||||||
|
0.724 | 0.400 | 17 | 63476833 | upstream gene variant | T/A;C | snv |
|
0.020 | 1.000 | 2 | 2006 | 2012 | |||||||||
|
0.724 | 0.400 | 17 | 63476833 | upstream gene variant | T/A;C | snv |
|
0.020 | 1.000 | 2 | 2006 | 2009 | |||||||||
|
0.724 | 0.400 | 17 | 63476833 | upstream gene variant | T/A;C | snv |
|
0.020 | 1.000 | 2 | 2006 | 2012 | |||||||||
|
17 | 63480868 | intron variant | A/G | snv | 0.45 |
|
0.020 | 1.000 | 2 | 2011 | 2013 | ||||||||||
|
0.851 | 0.120 | 17 | 63477287 | missense variant | G/A | snv | 2.1E-05 |
|
0.020 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.851 | 0.120 | 17 | 63477287 | missense variant | G/A | snv | 2.1E-05 |
|
0.020 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.851 | 0.120 | 17 | 63477287 | missense variant | G/A | snv | 2.1E-05 |
|
0.020 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
17 | 63487006 | synonymous variant | T/C | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||||
|
17 | 63487006 | synonymous variant | T/C | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||||
|
17 | 63477230 | missense variant | G/A | snv | 4.2E-05 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
1.000 | 0.120 | 17 | 63477150 | missense variant | T/C | snv | 2.8E-05 |
|
0.010 | 1.000 | 1 | 2003 | 2003 | ||||||||
|
0.851 | 0.160 | 17 | 63497137 | missense variant | C/T | snv |
|
0.010 | < 0.001 | 1 | 2006 | 2006 | |||||||||
|
0.851 | 0.160 | 17 | 63497137 | missense variant | C/T | snv |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||||
|
0.851 | 0.160 | 17 | 63497137 | missense variant | C/T | snv |
|
0.010 | < 0.001 | 1 | 2006 | 2006 | |||||||||
|
0.851 | 0.160 | 17 | 63497137 | missense variant | C/T | snv |
|
0.010 | < 0.001 | 1 | 2006 | 2006 | |||||||||
|
0.851 | 0.160 | 17 | 63497137 | missense variant | C/T | snv |
|
0.010 | < 0.001 | 1 | 2006 | 2006 | |||||||||
|
0.925 | 0.080 | 17 | 63479775 | missense variant | C/T | snv | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.080 | 17 | 63479775 | missense variant | C/T | snv | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
1.000 | 0.040 | 17 | 63489055 | missense variant | A/G | snv |
|
0.010 | 1.000 | 1 | 2009 | 2009 |