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 | 0.280 | 6 | 30365728 | upstream gene variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.807 | 0.280 | 6 | 30311353 | intron variant | G/A | snv | 6.6E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.807 | 0.360 | 6 | 31090563 | intergenic variant | C/A | snv | 7.4E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.807 | 0.120 | 15 | 78818751 | intron variant | C/T | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.807 | 0.320 | 6 | 31902549 | intron variant | G/A | snv | 7.7E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.807 | 0.360 | 6 | 31161533 | missense variant | C/T | snv | 7.0E-02 | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.807 | 0.200 | 15 | 78615690 | intron variant | A/G | snv | 0.29 |
|
0.710 | 1.000 | 1 | 2009 | 2014 | ||||||||
|
0.807 | 0.280 | 6 | 30070870 | 3 prime UTR variant | T/C;G | snv | 5.2E-02; 7.2E-06 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.827 | 0.080 | 15 | 78534606 | 3 prime UTR variant | T/C | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.160 | 6 | 29850791 | intron variant | T/C | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.280 | 6 | 32623148 | TF binding site variant | G/A | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.280 | 6 | 28986516 | intron variant | G/A | snv | 5.3E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.280 | 6 | 30360062 | upstream gene variant | G/T | snv | 7.1E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.827 | 0.160 | 5 | 1308437 | downstream gene variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.851 | 0.160 | 15 | 78497146 | synonymous variant | C/T | snv | 0.54 | 0.51 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.851 | 0.240 | 6 | 29474924 | downstream gene variant | C/T | snv | 5.3E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.851 | 0.080 | 15 | 78727268 | splice region variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.851 | 0.240 | 6 | 30685004 | missense variant | C/G;T | snv | 4.1E-06; 6.1E-02 |
|
0.700 | 1.000 | 1 | 2009 | 2009 |