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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.240 | 17 | 46003698 | intron variant | A/G | snv | 0.18 |
|
0.800 | 1.000 | 5 | 2009 | 2014 | ||||||||
|
0.827 | 0.200 | 17 | 45996523 | synonymous variant | A/G | snv | 0.14 | 0.15 |
|
0.730 | 0.750 | 1 | 2010 | 2012 | |||||||
|
0.882 | 0.120 | 17 | 45999299 | missense variant | A/G | snv | 0.14 | 0.15 |
|
0.730 | 0.750 | 1 | 2010 | 2017 | |||||||
|
0.925 | 0.120 | 17 | 45974480 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 |
|
0.720 | 1.000 | 2 | 2008 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45913906 | intron variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 4 | 2009 | 2014 | ||||||||
|
1.000 | 0.040 | 17 | 45979401 | non coding transcript exon variant | G/A | snv | 0.14 |
|
0.700 | 1.000 | 3 | 2009 | 2012 | ||||||||
|
0.925 | 0.120 | 17 | 45990034 | missense variant | T/C | snv | 0.15 | 0.15 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45990316 | intron variant | G/A | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 17 | 45991558 | synonymous variant | G/A;T | snv | 0.14; 8.0E-05 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 17 | 46025238 | 3 prime UTR variant | T/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 17 | 45998535 | intron variant | A/G | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 17 | 45934459 | intron variant | A/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 17 | 45993723 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.120 | 17 | 46027143 | 3 prime UTR variant | T/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.120 | 17 | 45962325 | 5 prime UTR variant | A/G | snv | 0.14 | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.882 | 0.160 | 17 | 45983912 | missense variant | C/T | snv | 0.15 | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.120 | 17 | 45996607 | synonymous variant | T/C | snv | 0.14 | 0.15 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45893296 | intron variant | G/T | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 17 | 45892788 | intron variant | T/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.882 | 0.160 | 17 | 45900461 | intron variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 17 | 46006036 | intron variant | G/A | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 17 | 45896132 | non coding transcript exon variant | T/G | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 17 | 45921456 | intron variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2011 | 2011 |