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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv |
|
0.740 | 1.000 | 4 | 2001 | 2019 | |||||||||
|
0.851 | 0.080 | 13 | 28028203 | missense variant | G/C;T | snv |
|
0.720 | 1.000 | 2 | 2013 | 2016 | |||||||||
|
1.000 | 0.040 | 13 | 28027222 | missense variant | A/C;T | snv |
|
0.710 | 1.000 | 1 | 2012 | 2019 | |||||||||
|
0.925 | 0.040 | 13 | 28028244 | missense variant | T/G | snv |
|
0.710 | 1.000 | 1 | 2006 | 2006 | |||||||||
|
0.925 | 0.120 | 13 | 28018500 | missense variant | G/C | snv |
|
0.710 | 1.000 | 1 | 2003 | 2014 | |||||||||
|
1.000 | 0.040 | 13 | 28018483 | missense variant | T/C | snv | 2.4E-05 | 1.4E-05 |
|
0.710 | 1.000 | 1 | 2005 | 2014 | |||||||
|
0.851 | 0.080 | 13 | 28028203 | missense variant | G/C;T | snv |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.851 | 0.080 | 13 | 28028203 | missense variant | G/C;T | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.851 | 0.080 | 13 | 28028203 | missense variant | G/C;T | snv |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.851 | 0.080 | 13 | 28028203 | missense variant | G/C;T | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.925 | 0.040 | 13 | 28028244 | missense variant | T/G | snv |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||||
|
1.000 | 0.040 | 13 | 28028234 | missense variant | G/A | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv |
|
0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv |
|
0.010 | 1.000 | 1 | 2004 | 2004 | |||||||||
|
1.000 | 0.120 | 13 | 28020665 | intron variant | T/C | snv | 0.28 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.040 | 13 | 28052566 | missense variant | A/G | snv |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.925 | 0.080 | 13 | 28036046 | splice region variant | A/G | snv | 0.71 | 0.61 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 13 | 28036046 | splice region variant | A/G | snv | 0.71 | 0.61 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.040 | 13 | 28049450 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 |
|
0.010 | < 0.001 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.040 | 13 | 28049450 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.040 | 13 | 28049450 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.851 | 0.040 | 13 | 28049450 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
1.000 | 0.120 | 13 | 28034336 | missense variant | C/T | snv | 1.3E-02 | 5.0E-02 |
|
0.010 | 1.000 | 1 | 2019 | 2019 |