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 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 |
|
0.800 | 1.000 | 2 | 2012 | 2015 | ||||||||
|
0.827 | 0.200 | 16 | 28528527 | downstream gene variant | C/T | snv | 0.36 |
|
0.800 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.807 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 2 | 2015 | 2016 | ||||||||
|
0.807 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 2 | 2015 | 2016 | ||||||||
|
16 | 28527319 | regulatory region variant | A/G | snv | 0.33 |
|
0.700 | 1.000 | 2 | 2017 | 2018 | ||||||||||
|
16 | 28517302 | intergenic variant | T/C | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.742 | 0.440 | 16 | 28502082 | missense variant | A/G | snv | 0.28 | 0.24 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.742 | 0.440 | 16 | 28502082 | missense variant | A/G | snv | 0.28 | 0.24 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
16 | 28503533 | intron variant | G/T | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 28513291 | upstream gene variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
0.807 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.807 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.807 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | 16 | 28517460 | intergenic variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.040 | 16 | 28517460 | intergenic variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.040 | 16 | 28511823 | splice region variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.040 | 16 | 28511823 | splice region variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
16 | 28515900 | upstream gene variant | C/T | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
16 | 28516005 | upstream gene variant | G/A | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2018 | 2018 |