| 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 | 6 | 12888772 | intron variant | C/T | snv | 0.61 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 4 | 147126398 | intron variant | C/T | snv | 0.70 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.120 | 1 | 56497149 | intron variant | A/G | snv | 0.11 |
|
0.800 | 1.000 | 1 | 2011 | 2014 | ||||||||
|
1.000 | 0.040 | 6 | 35067023 | intron variant | G/C | snv | 0.14 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 4 | 155590307 | intergenic variant | G/T | snv | 0.50 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.851 | 0.160 | 15 | 78787892 | intron variant | C/T | snv | 0.30 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 2 | 19745816 | intergenic variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.040 | 17 | 2223210 | intron variant | G/C | snv | 0.35 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.080 | 1 | 154465420 | 3 prime UTR variant | T/A;C | snv | 0.80 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.040 | 3 | 138401110 | intron variant | T/C | snv | 0.12 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.080 | 10 | 30046193 | intron variant | T/C | snv | 0.33 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.080 | 14 | 99667605 | intron variant | T/A;C | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.040 | 6 | 159225301 | intron variant | T/C | snv | 0.38 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 10 | 30027143 | missense variant | C/A;G | snv | 4.0E-06; 0.38 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.160 | 12 | 110912851 | intron variant | A/G | snv | 7.1E-02 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.807 | 0.120 | 15 | 78796769 | missense variant | A/G | snv | 0.34 | 0.33 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 15 | 84545426 | intron variant | T/C | snv | 5.6E-05 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.807 | 0.120 | 15 | 78818751 | intron variant | C/T | snv | 0.34 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2016 | |||||||||
|
0.807 | 0.120 | 17 | 48911235 | non coding transcript exon variant | C/T | snv | 0.40 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.882 | 0.120 | 9 | 133266790 | intron variant | C/A;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.716 | 0.360 | 9 | 22029548 | 3 prime UTR variant | T/C | snv | 0.31 | 0.28 |
|
0.800 | 1.000 | 1 | 2011 | 2018 | |||||||
|
0.752 | 0.320 | 9 | 133278724 | upstream gene variant | C/T | snv | 0.81 |
|
0.800 | 1.000 | 1 | 2011 | 2014 | ||||||||
|
1.000 | 0.040 | X | 110695977 | intron variant | T/G | snv | 0.50 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 |
|
0.800 | 1.000 | 1 | 2012 | 2016 |