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 | 0.200 | 11 | 112233502 | missense variant | A/G | snv | 2.1E-05 |
|
0.010 | 1.000 | 1 | 1997 | 1997 | ||||||||
|
0.882 | 0.200 | 11 | 112233502 | missense variant | A/G | snv | 2.1E-05 |
|
0.010 | 1.000 | 1 | 1997 | 1997 | ||||||||
|
0.882 | 0.200 | 11 | 112233502 | missense variant | A/G | snv | 2.1E-05 |
|
0.010 | 1.000 | 1 | 1997 | 1997 | ||||||||
|
0.882 | 0.120 | 11 | 112228665 | missense variant | A/G | snv | 1.2E-04 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2001 | 2001 | |||||||
|
0.882 | 0.120 | 11 | 112228665 | missense variant | A/G | snv | 1.2E-04 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 1998 | 1998 | |||||||
|
0.882 | 0.120 | 11 | 112233178 | missense variant | C/G;T | snv | 4.0E-06; 7.6E-05 |
|
0.010 | 1.000 | 1 | 1998 | 1998 | ||||||||
|
0.882 | 0.120 | 11 | 112233178 | missense variant | C/G;T | snv | 4.0E-06; 7.6E-05 |
|
0.010 | 1.000 | 1 | 2001 | 2001 | ||||||||
|
0.925 | 0.120 | 11 | 112230210 | missense variant | G/A;C | snv | 1.6E-05; 8.0E-06 |
|
0.010 | 1.000 | 1 | 1998 | 1998 | ||||||||
|
0.925 | 0.120 | 11 | 112233205 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 1998 | 1998 | |||||||
|
0.925 | 0.120 | 11 | 112226516 | stop gained | C/G;T | snv |
|
0.010 | 1.000 | 1 | 1998 | 1998 | |||||||||
|
0.925 | 0.120 | 11 | 112233434 | missense variant | C/T | snv | 1.2E-04 | 9.8E-05 |
|
0.010 | 1.000 | 1 | 1998 | 1998 | |||||||
|
1.000 | 0.120 | 11 | 112226489 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 |
|
0.700 | 1.000 | 12 | 1994 | 2001 | |||||||
|
0.925 | 0.120 | 11 | 112228649 | missense variant | A/G | snv | 4.0E-06 |
|
0.700 | 1.000 | 12 | 1994 | 2001 | ||||||||
|
1.000 | 0.120 | 11 | 112226521 | missense variant | G/T | snv | 1.0E-05 |
|
0.700 | 1.000 | 12 | 1994 | 2001 | ||||||||
|
1.000 | 0.120 | 11 | 112228618 | missense variant | C/G | snv | 4.1E-06 |
|
0.700 | 1.000 | 12 | 1994 | 2001 | ||||||||
|
1.000 | 0.120 | 11 | 112233215 | missense variant | A/G | snv |
|
0.700 | 1.000 | 12 | 1994 | 2001 | |||||||||
|
1.000 | 0.120 | 11 | 112233457 | missense variant | A/G | snv |
|
0.700 | 1.000 | 12 | 1994 | 2001 | |||||||||
|
1.000 | 0.120 | 11 | 112233208 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 |
|
0.700 | 1.000 | 12 | 1994 | 2001 | |||||||
|
1.000 | 0.120 | 11 | 112230210 | inframe deletion | GTG/- | delins | 8.0E-06 | 2.1E-05 |
|
0.700 | 1.000 | 5 | 1995 | 2016 | |||||||
|
1.000 | 0.120 | 11 | 112228591 | splice region variant | C/G;T | snv | 2.4E-04 |
|
0.700 | 1.000 | 4 | 1997 | 2017 | ||||||||
|
1.000 | 0.120 | 11 | 112228626 | frameshift variant | TTTG/- | delins | 4.0E-06 | 7.2E-06 |
|
0.700 | 1.000 | 4 | 2001 | 2013 | |||||||
|
1.000 | 0.120 | 11 | 112233507 | frameshift variant | A/- | delins | 1.6E-05 |
|
0.700 | 1.000 | 2 | 2009 | 2010 | ||||||||
|
1.000 | 0.120 | 11 | 112230681 | splice donor variant | -/GG | delins |
|
0.700 | 1.000 | 2 | 1987 | 2006 | |||||||||
|
1.000 | 0.120 | 11 | 112233216 | stop gained | C/A | snv | 2.8E-05 | 1.4E-05 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.040 | 11 | 112247868 | intron variant | AT/-;ATAT | delins | 5.3E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |