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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.200 | 6 | 32203906 | intron variant | T/C | snv | 0.48 | 0.46 |
|
0.810 | 1.000 | 1 | 2012 | 2012 | |||||||
|
6 | 32223562 | intron variant | C/T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
0.925 | 0.160 | 6 | 32216568 | non coding transcript exon variant | T/C | snv | 0.21 |
|
0.810 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
6 | 32211932 | intron variant | A/G | snv | 5.5E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.120 | 6 | 32209005 | intron variant | G/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.120 | 6 | 32197667 | intron variant | A/G | snv | 0.13 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 6 | 32197667 | intron variant | A/G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.040 | 6 | 32223264 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32212119 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.807 | 0.280 | 6 | 32220606 | missense variant | T/C | snv | 0.40 | 0.40 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.752 | 0.280 | 6 | 32212119 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.120 | 6 | 32209005 | intron variant | G/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.752 | 0.280 | 6 | 32223562 | intron variant | C/T | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
6 | 32222843 | intron variant | T/C | snv | 0.35 | 0.37 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.040 | 6 | 32205822 | intron variant | T/C | snv | 1.8E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.080 | 6 | 32224554 | upstream gene variant | A/G;T | snv |
|
0.700 | 1.000 | 2 | 2013 | 2018 | |||||||||
|
6 | 32222211 | intron variant | TCT/- | delins | 0.26 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |