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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 |
|
0.800 | 1.000 | 2 | 2011 | 2013 | |||||||
|
1.000 | 0.040 | 12 | 110902439 | intron variant | T/C | snv | 0.36 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 |
|
0.700 | 1.000 | 2 | 2011 | 2013 | |||||||
|
0.851 | 0.160 | 12 | 110912851 | intron variant | A/G | snv | 7.1E-02 |
|
0.700 | 1.000 | 2 | 2011 | 2013 | ||||||||
|
0.925 | 0.080 | 12 | 110895818 | intron variant | T/C | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.040 | 12 | 110856716 | intron variant | A/G | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.080 | 12 | 110900990 | intron variant | C/T | snv | 6.1E-02 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.040 | 12 | 110917522 | intron variant | G/A | snv | 4.7E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 110876485 | intron variant | T/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.040 | 12 | 111154576 | intron variant | G/T | snv | 7.7E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 110874125 | intron variant | T/C | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.040 | 12 | 110912967 | intron variant | C/T | snv | 7.1E-02 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 110953995 | intron variant | C/T | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 110958809 | non coding transcript exon variant | C/T | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 12 | 111792215 | intron variant | G/A;C | snv | 1.9E-02 | 5.8E-03 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 12 | 110949157 | intron variant | T/C | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 110955715 | non coding transcript exon variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.040 | 12 | 110963512 | downstream gene variant | G/T | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 111152688 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 111180528 | intron variant | T/G | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.040 | 12 | 111196477 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.040 | 12 | 111229180 | intron variant | C/T | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2011 | 2011 |