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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11 | 61779765 | intron variant | C/T | snv | 0.27 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||||
|
1.000 | 0.080 | 11 | 61776027 | intron variant | T/C | snv | 0.42 | 0.42 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | |||||||
|
1.000 | 0.080 | 11 | 61781986 | non coding transcript exon variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | |||||||
|
11 | 61784455 | non coding transcript exon variant | A/C | snv | 0.29 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||||
|
0.708 | 0.400 | 11 | 61785208 | non coding transcript exon variant | G/T | snv | 0.28 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||
|
11 | 61779765 | intron variant | C/T | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61771548 | synonymous variant | C/G;T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61771548 | synonymous variant | C/G;T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61771134 | intron variant | A/G | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 11 | 61776027 | intron variant | T/C | snv | 0.42 | 0.42 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
11 | 61776489 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 11 | 61779120 | non coding transcript exon variant | A/G | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
11 | 61781402 | intron variant | G/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61781402 | intron variant | G/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.763 | 0.160 | 11 | 61781553 | intron variant | G/A | snv | 0.37 | 0.29 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 11 | 61781986 | non coding transcript exon variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 11 | 61781986 | non coding transcript exon variant | A/G | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |