Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
18 | 74823326 | intron variant | G/A | snv | 0.25 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
18 | 74589381 | downstream gene variant | A/C | snv | 0.72 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
18 | 74633832 | inframe insertion | -/AGT | delins |
|
0.700 | 0 | ||||||||||||||
|
18 | 74633832 | inframe insertion | -/AGT | delins |
|
0.700 | 0 | ||||||||||||||
|
1.000 | 0.040 | 18 | 74669985 | intron variant | C/T | snv | 8.4E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 18 | 74661615 | intron variant | T/A | snv | 0.40 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 18 | 74668931 | intron variant | G/A;T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 18 | 74637673 | intron variant | T/A;C | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 18 | 74669112 | intron variant | G/A | snv | 0.15 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 18 | 74632282 | synonymous variant | C/T | snv | 9.3E-02 | 0.11 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1.000 | 0.040 | 18 | 74632267 | synonymous variant | T/C | snv | 0.15 | 0.20 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1.000 | 0.040 | 18 | 74668190 | intron variant | T/A;C | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 18 | 74648959 | intron variant | T/C | snv | 0.10 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 18 | 74675179 | intron variant | G/A | snv | 0.27 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 18 | 74666435 | intron variant | C/T | snv | 0.51 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 18 | 74666435 | intron variant | C/T | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.040 | 18 | 74666435 | intron variant | C/T | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.040 | 18 | 74633934 | missense variant | A/C | snv | 0.15 | 0.20 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 |