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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17 | 7675207 | missense variant | G/A;C | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
17 | 7676187 | missense variant | T/C | snv | 4.0E-06 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
17 | 7676171 | missense variant | C/T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||||||
|
17 | 7673743 | missense variant | C/A;T | snv | 8.0E-06; 8.0E-06 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
17 | 7676113 | missense variant | C/T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||||
|
17 | 7675221 | missense variant | T/A | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
17 | 7674203 | missense variant | T/C | snv | 1.6E-05 | 7.0E-06 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
17 | 7675199 | missense variant | G/A;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
17 | 7675053 | missense variant | C/T | snv | 7.0E-06 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2004 | 2004 | |||||||||
|
17 | 7673714 | frameshift variant | C/- | delins |
|
Neoplasms | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
17 | 7675109 | missense variant | T/C | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
17 | 7676171 | frameshift variant | C/- | del |
|
Neoplasms | 0.010 | 1.000 | 1 | 2002 | 2002 | ||||||||||
|
17 | 7676023 | splice donor variant | A/C | snv | 8.0E-06 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 |
|
Neoplasms | 0.100 | 0.971 | 34 | 2003 | 2018 | |||||||
|
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 | ||||||||
|
0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 |
|
Neoplasms | 0.780 | 1.000 | 9 | 1995 | 2020 | |||||||
|
0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 |
|
Neoplasms | 0.770 | 1.000 | 9 | 2012 | 2020 | |||||||
|
0.605 | 0.600 | 17 | 7675088 | missense variant | C/A;T | snv | 4.0E-06 |
|
Neoplasms | 0.780 | 0.909 | 11 | 2000 | 2019 | |||||||
|
0.605 | 0.680 | 17 | 7674221 | missense variant | G/A;C | snv | 4.0E-06 |
|
Neoplasms | 0.760 | 0.857 | 7 | 1999 | 2019 | |||||||
|
0.611 | 0.520 | 17 | 7673803 | missense variant | G/A;C;T | snv | 1.2E-05 |
|
Neoplasms | 0.710 | 1.000 | 2 | 2014 | 2014 | |||||||
|
0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 |
|
Neoplasms | 0.100 | 0.947 | 19 | 2007 | 2020 | |||||||
|
0.627 | 0.400 | 17 | 7673751 | missense variant | C/A;G;T | snv | 1.6E-04 | 1.3E-04 |
|
Neoplasms | 0.100 | 0.900 | 10 | 2014 | 2019 | ||||||
|
0.630 | 0.320 | 17 | 7670699 | missense variant | C/A;G;T | snv | 1.2E-05 |
|
Neoplasms | 0.100 | 0.875 | 16 | 2001 | 2020 | |||||||
|
0.641 | 0.400 | 17 | 7674230 | missense variant | C/A;G;T | snv |
|
Neoplasms | 0.740 | 1.000 | 6 | 2006 | 2018 |