Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins |
|
Neoplasms | 0.100 | 0.966 | 29 | 2003 | 2018 | ||||||||
|
0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv |
|
Neoplasms | 0.100 | 0.966 | 29 | 2003 | 2018 | ||||||||
|
0.716 | 0.120 | 17 | 7675097 | missense variant | A/C;G | snv |
|
Neoplasms | 0.060 | 0.833 | 6 | 2010 | 2019 | ||||||||
|
0.641 | 0.400 | 17 | 7674230 | missense variant | C/A;G;T | snv |
|
Neoplasms | 0.740 | 1.000 | 6 | 2006 | 2018 | ||||||||
|
0.645 | 0.360 | 17 | 7674216 | missense variant | C/A;G | snv |
|
Neoplasms | 0.050 | 1.000 | 5 | 2001 | 2013 | ||||||||
|
0.677 | 0.400 | 17 | 7673826 | missense variant | A/G | snv |
|
Neoplasms | 0.040 | 1.000 | 4 | 2008 | 2019 | ||||||||
|
0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv |
|
Neoplasms | 0.020 | 1.000 | 2 | 2007 | 2019 | ||||||||
|
0.742 | 0.400 | 17 | 7674890 | missense variant | T/A;C;G | snv |
|
Neoplasms | 0.020 | 1.000 | 2 | 1991 | 2008 | ||||||||
|
0.882 | 0.080 | 17 | 7674971 | missense variant | C/T | snv |
|
Neoplasms | 0.020 | 1.000 | 2 | 2013 | 2015 | ||||||||
|
0.708 | 0.400 | 17 | 7674262 | missense variant | T/C;G | snv |
|
Neoplasms | 0.020 | 1.000 | 2 | 2008 | 2019 | ||||||||
|
0.925 | 0.040 | 17 | 7674956 | missense variant | T/C | snv |
|
Neoplasms | 0.020 | 1.000 | 2 | 2017 | 2017 | ||||||||
|
0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 |
|
Neoplasms | 0.020 | 1.000 | 2 | 2015 | 2019 | |||||||
|
0.716 | 0.280 | 17 | 7675094 | missense variant | A/C;G;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
17 | 7675207 | missense variant | G/A;C | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.677 | 0.360 | 17 | 7674886 | missense variant | A/C;G | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 1995 | 1995 | ||||||||
|
0.925 | 0.080 | 17 | 7674190 | missense variant | T/C;G | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.280 | 17 | 7675167 | frameshift variant | A/-;AA | delins |
|
Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.120 | 17 | 7673767 | missense variant | C/T | snv | 7.0E-06 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.080 | 17 | 7675207 | frameshift variant | GCA/CC | delins |
|
Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
17 | 7676171 | missense variant | C/T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||||||
|
0.695 | 0.440 | 17 | 7673823 | missense variant | C/A;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
0.925 | 0.160 | 17 | 7675131 | missense variant | C/T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 17 | 7675212 | missense variant | A/G;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.732 | 0.320 | 17 | 7674237 | missense variant | G/A;C | snv |
|
Neoplasms | 0.010 | < 0.001 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.120 | 17 | 7670669 | missense variant | G/A;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2006 | 2006 |