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 | 0.040 | 10 | 100152437 | intron variant | C/T | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.040 | 10 | 100267650 | 5 prime UTR variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
2 | 101025798 | intron variant | A/G | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
12 | 101480178 | intron variant | C/T | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
15 | 101528701 | upstream gene variant | C/T | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
4 | 101786634 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 |
|
0.800 | 1.000 | 4 | 2010 | 2018 | ||||||||
|
4 | 102276925 | intron variant | A/G | snv | 5.1E-02 |
|
0.700 | 1.000 | 3 | 2015 | 2019 | ||||||||||
|
0.851 | 0.120 | 4 | 102363708 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 2 | 2016 | 2018 | |||||||||
|
11 | 10367235 | intron variant | A/G | snv | 0.29 |
|
0.800 | 1.000 | 2 | 2010 | 2013 | ||||||||||
|
9 | 104753533 | intron variant | C/T | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
14 | 104792555 | intron variant | C/T | snv | 0.51 | 0.48 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
9 | 104800276 | intron variant | G/A | snv | 0.60 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
14 | 104806341 | downstream gene variant | A/T | snv | 0.45 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||||
|
14 | 104810872 | downstream gene variant | G/A;C | snv |
|
0.800 | 1.000 | 2 | 2013 | 2017 | |||||||||||
|
9 | 104826047 | intron variant | G/A | snv | 5.8E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
9 | 104826853 | intron variant | A/T | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
9 | 104827286 | intron variant | C/T | snv | 5.8E-02 |
|
0.700 | 1.000 | 2 | 2016 | 2019 | ||||||||||
|
9 | 104827463 | intron variant | C/T | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
9 | 104828991 | synonymous variant | G/T | snv | 0.20 | 0.23 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | |||||||||
|
1.000 | 0.040 | 9 | 104832083 | intron variant | A/G | snv | 0.16 |
|
0.800 | 1.000 | 2 | 2011 | 2019 | ||||||||
|
1.000 | 0.040 | 9 | 104839260 | intron variant | G/A | snv | 0.47 |
|
0.700 | 1.000 | 3 | 2016 | 2019 | ||||||||
|
0.790 | 0.160 | 9 | 104858554 | missense variant | G/A | snv | 1.3E-02 | 4.4E-03 |
|
0.800 | 1.000 | 3 | 2008 | 2019 | |||||||
|
9 | 104884738 | intron variant | C/T | snv | 0.11 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||||
|
1.000 | 0.040 | 9 | 104884939 | intron variant | C/T | snv | 0.46 |
|
0.800 | 1.000 | 1 | 2008 | 2008 |