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 | 0.160 | 6 | 151842664 | start lost | A/G | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
1.000 | 0.040 | 17 | 50356597 | synonymous variant | T/C | snv | 0.44 | 0.47 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
1.000 | 0.040 | 16 | 17141171 | synonymous variant | G/A | snv | 1.6E-05 | 1.4E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | |||||||
|
0.925 | 0.040 | 13 | 46593768 | intron variant | A/G | snv | 0.84 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 |
|
0.020 | 1.000 | 2 | 2006 | 2007 | |||||||
|
0.752 | 0.280 | 2 | 112832890 | intron variant | C/G;T | snv |
|
0.010 | 1.000 | 1 | 2007 | 2007 | |||||||||
|
1.000 | 0.040 | 1 | 186755871 | intergenic variant | G/A | snv | 0.93 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.040 | 6 | 116806885 | missense variant | T/C | snv | 1.2E-04 | 3.5E-05 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.732 | 0.240 | 2 | 182834857 | missense variant | G/A;C;T | snv | 8.0E-05; 8.0E-02; 5.6E-05 |
|
0.050 | 0.800 | 5 | 2005 | 2009 | ||||||||
|
0.807 | 0.120 | 2 | 182838608 | missense variant | G/A | snv | 8.2E-02 | 8.3E-02 |
|
0.030 | 0.667 | 3 | 2005 | 2009 | |||||||
|
1.000 | 0.040 | 9 | 111040905 | upstream gene variant | C/T | snv | 0.18 |
|
0.020 | 0.500 | 2 | 2008 | 2009 | ||||||||
|
0.882 | 0.080 | 3 | 15175196 | non coding transcript exon variant | A/G;T | snv | 0.21 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.637 | 0.600 | 22 | 46198429 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.040 | 15 | 33783099 | intron variant | T/C | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv |
|
0.010 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
1.000 | 0.040 | 12 | 47982354 | intron variant | G/A | snv | 0.38 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
1.000 | 0.040 | 12 | 47997633 | synonymous variant | G/A;T | snv | 8.1E-06; 0.21 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.040 | 15 | 68789051 | intron variant | T/C | snv | 0.27 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.605 | 0.800 | 7 | 22726602 | non coding transcript exon variant | A/G | snv | 0.72 |
|
0.020 | 1.000 | 2 | 2008 | 2010 | ||||||||
|
1.000 | 0.040 | 15 | 51255741 | 5 prime UTR variant | C/G | snv | 0.35 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.605 | 0.760 | 2 | 112836810 | 5 prime UTR variant | G/A | snv | 0.56 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.040 | 6 | 116131040 | intron variant | T/G | snv | 0.50 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.040 | 2 | 102157594 | intron variant | G/A | snv | 0.39 |
|
0.010 | 1.000 | 1 | 2010 | 2010 |