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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 |
|
0.700 | 1.000 | 4 | 2007 | 2011 | ||||||||
|
0.752 | 0.360 | 6 | 32609603 | intergenic variant | A/G | snv | 0.19 |
|
0.810 | 1.000 | 4 | 2007 | 2018 | ||||||||
|
0.763 | 0.360 | 6 | 32584333 | missense variant | C/G | snv | 1.3E-05 |
|
0.030 | 1.000 | 3 | 1998 | 2003 | ||||||||
|
0.763 | 0.360 | 6 | 32584333 | missense variant | C/G | snv | 1.3E-05 |
|
0.020 | 1.000 | 2 | 1998 | 1999 | ||||||||
|
0.763 | 0.360 | 6 | 32584333 | missense variant | C/G | snv | 1.3E-05 |
|
0.020 | 0.500 | 2 | 2003 | 2005 | ||||||||
|
0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 |
|
0.710 | 1.000 | 2 | 2013 | 2016 | ||||||||
|
0.882 | 0.120 | 6 | 32610275 | intergenic variant | G/A | snv | 0.43 |
|
0.700 | 1.000 | 2 | 2010 | 2012 | ||||||||
|
0.851 | 0.240 | 6 | 32606394 | intergenic variant | G/A;C | snv |
|
0.800 | 1.000 | 2 | 2007 | 2011 | |||||||||
|
0.752 | 0.360 | 6 | 32609603 | intergenic variant | A/G | snv | 0.19 |
|
0.810 | 1.000 | 2 | 2011 | 2015 | ||||||||
|
0.925 | 0.120 | 6 | 32608701 | regulatory region variant | T/A;C | snv |
|
0.800 | 1.000 | 2 | 2009 | 2013 | |||||||||
|
6 | 32580773 | synonymous variant | G/A | snv | 7.2E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.080 | 6 | 32584314 | missense variant | G/A;C;T | snv | 1.1E-02; 1.8E-05 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 6 | 32578889 | 3 prime UTR variant | G/A;C;T | snv | 2.6E-02 | 2.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
6 | 32591382 | upstream gene variant | C/T | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.040 | 6 | 32587108 | intron variant | C/T | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 6 | 32584355 | missense variant | T/A;C;G | snv | 0.25; 2.7E-02; 4.7E-05; 1.6E-05; 7.6E-03 |
|
0.010 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
0.882 | 0.080 | 6 | 32584354 | missense variant | C/A;G;T | snv | 8.9E-03; 0.23; 1.2E-04 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.882 | 0.080 | 6 | 32584354 | missense variant | C/A;G;T | snv | 8.9E-03; 0.23; 1.2E-04 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.882 | 0.080 | 6 | 32584354 | missense variant | C/A;G;T | snv | 8.9E-03; 0.23; 1.2E-04 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 6 | 32604965 | intergenic variant | C/G | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.040 | 6 | 32607947 | intergenic variant | T/C | snv | 4.7E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 6 | 32607948 | intergenic variant | G/A | snv | 4.7E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
6 | 32602155 | intergenic variant | T/A | snv | 4.4E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.040 | 6 | 32584671 | intron variant | A/C | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 6 | 32584671 | intron variant | A/C | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2017 | 2017 |