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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.120 | 10 | 62621908 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 10 | 62621908 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 10 | 62621908 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 10 | 62621908 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.827 | 0.120 | 10 | 62621908 | intron variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.040 | 10 | 62658896 | non coding transcript exon variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
10 | 62427805 | intron variant | C/G;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
0.925 | 0.120 | 10 | 62655424 | missense variant | A/C;G | snv | 0.80 |
|
0.810 | 1.000 | 1 | 2011 | 2012 | ||||||||
|
10 | 62418898 | intron variant | -/ATAACTTT;ATAATTTT;ATAGTTTT | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
0.925 | 0.120 | 10 | 62610240 | intron variant | C/G | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.925 | 0.120 | 10 | 62610240 | intron variant | C/G | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
10 | 62622599 | intron variant | A/C | snv | 0.65 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
0.851 | 0.040 | 10 | 62637778 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||
|
0.851 | 0.040 | 10 | 62637778 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.851 | 0.040 | 10 | 62637778 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.851 | 0.040 | 10 | 62637778 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
10 | 62671446 | non coding transcript exon variant | T/C | snv | 6.2E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
10 | 62671446 | non coding transcript exon variant | T/C | snv | 6.2E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.040 | 10 | 62421587 | intron variant | T/C | snv | 3.0E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.040 | 10 | 62421587 | intron variant | T/C | snv | 3.0E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.040 | 10 | 62642673 | intron variant | G/A | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.040 | 10 | 62642673 | intron variant | G/A | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.882 | 0.040 | 10 | 62642673 | intron variant | G/A | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.120 | 10 | 62638706 | intron variant | C/T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
10 | 62637156 | intron variant | C/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |