Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.120 | MT | 15607 | synonymous variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15670 | synonymous variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 14743 | upstream gene variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 14753 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 14784 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15058 | synonymous variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15328 | synonymous variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15334 | synonymous variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15363 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15890 | non coding transcript exon variant | C/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15932 | non coding transcript exon variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15061 | synonymous variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15148 | synonymous variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | MT | 15259 | synonymous variant | C/T | snv | 0.700 | 0 |