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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 15 | 88856723 | missense variant | G/T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 15 | 88857646 | missense variant | T/A | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.040 | 15 | 88872944 | missense variant | G/A | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 15 | 88858712 | stop gained | G/A;T | snv |
|
0.700 | 1.000 | 11 | 1990 | 2017 | ||||||||||
|
1.000 | 15 | 88858712 | stop gained | G/A;T | snv |
|
0.700 | 1.000 | 11 | 1990 | 2017 | ||||||||||
|
15 | 88852395 | intron variant | A/G | snv | 0.68 |
|
0.700 | 1.000 | 4 | 2010 | 2017 | ||||||||||
|
1.000 | 0.040 | 15 | 88861672 | intron variant | A/T | snv | 5.3E-03 |
|
0.020 | 1.000 | 2 | 2011 | 2014 | ||||||||
|
15 | 88845674 | synonymous variant | C/T | snv | 3.8E-02 | 6.4E-02 |
|
0.700 | 1.000 | 2 | 2010 | 2019 | |||||||||
|
15 | 88845674 | synonymous variant | C/T | snv | 3.8E-02 | 6.4E-02 |
|
0.700 | 1.000 | 2 | 2010 | 2011 | |||||||||
|
15 | 88852395 | intron variant | A/G | snv | 0.68 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||||
|
15 | 88870012 | intron variant | T/C | snv | 0.27 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||||
|
1.000 | 0.040 | 15 | 88860173 | intron variant | G/A | snv | 0.13 |
|
0.020 | 1.000 | 2 | 2011 | 2014 | ||||||||
|
15 | 88816458 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 2 | 2008 | 2019 | |||||||||||
|
15 | 88869048 | intron variant | A/G | snv | 0.43 |
|
0.700 | 1.000 | 2 | 2014 | 2019 | ||||||||||
|
1.000 | 0.040 | 15 | 88859008 | synonymous variant | T/A;C | snv | 0.73 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
15 | 88844673 | intron variant | A/G | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 88813601 | intron variant | G/T | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 88825873 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
15 | 88825873 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1.000 | 0.080 | 15 | 88872038 | missense variant | G/A | snv |
|
0.800 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
1.000 | 0.160 | 15 | 88847281 | missense variant | T/A;C | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.080 | 15 | 88867083 | intron variant | T/G | snv | 0.44 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
15 | 88840533 | intron variant | T/C | snv | 2.2E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
15 | 88845033 | intron variant | A/G | snv | 3.3E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 88845033 | intron variant | A/G | snv | 3.3E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |