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 | 0.120 | 6 | 30105418 | non coding transcript exon variant | A/C | snv | 0.73 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.925 | 0.120 | 6 | 30110190 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
1.000 | 0.040 | 6 | 30103983 | non coding transcript exon variant | T/C | snv | 7.2E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
6 | 30108087 | missense variant | A/C;G | snv | 4.1E-06; 0.68 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
0.851 | 0.280 | 6 | 30112497 | synonymous variant | G/A | snv | 0.14 | 0.13 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.851 | 0.280 | 6 | 30112497 | synonymous variant | G/A | snv | 0.14 | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.851 | 0.280 | 6 | 30112497 | synonymous variant | G/A | snv | 0.14 | 0.13 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.851 | 0.280 | 6 | 30112497 | synonymous variant | G/A | snv | 0.14 | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 |
|
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 | 2007 | 2007 | ||||||||
|
0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.827 | 0.280 | 6 | 30110498 | missense variant | C/T | snv | 0.12 | 0.12 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.827 | 0.280 | 6 | 30110498 | missense variant | C/T | snv | 0.12 | 0.12 |
|
0.800 | 1.000 | 1 | 2007 | 2015 | |||||||
|
0.827 | 0.280 | 6 | 30110498 | missense variant | C/T | snv | 0.12 | 0.12 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.827 | 0.280 | 6 | 30110498 | missense variant | C/T | snv | 0.12 | 0.12 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.120 | 6 | 30109452 | intron variant | A/G | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.925 | 0.120 | 6 | 30106070 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 6 | 30106070 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 6 | 30106070 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 6 | 30106070 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 6 | 30106070 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 6 | 30110190 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2011 | 2011 |