PCAT1, prostate cancer associated transcript 1, 100750225
N. diseases: 90; N. variants: 91
Source: ALL
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.716 | 0.360 | 8 | 127343372 | intron variant | A/G | snv | 0.43 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.800 | 0.864 | 22 | 2007 | 2017 | |||||||
|
0.724 | 0.480 | 8 | 127112671 | intron variant | C/A | snv | 0.16 |
|
Neoplasms; Male Urogenital Diseases | 0.800 | 0.955 | 22 | 2007 | 2019 | |||||||
|
0.716 | 0.360 | 8 | 127343372 | intron variant | A/G | snv | 0.43 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.800 | 0.850 | 20 | 2007 | 2016 | |||||||
|
0.724 | 0.480 | 8 | 127112671 | intron variant | C/A | snv | 0.16 |
|
Neoplasms; Male Urogenital Diseases | 0.800 | 0.950 | 20 | 2007 | 2018 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.890 | 0.938 | 16 | 2007 | 2019 | |||||||
|
0.925 | 0.080 | 8 | 127094635 | intron variant | A/C | snv | 0.17 |
|
Neoplasms; Male Urogenital Diseases | 0.780 | 1.000 | 10 | 2008 | 2017 | |||||||
|
0.925 | 0.080 | 8 | 127094635 | intron variant | A/C | snv | 0.17 |
|
Neoplasms; Male Urogenital Diseases | 0.780 | 1.000 | 9 | 2008 | 2017 | |||||||
|
0.732 | 0.240 | 8 | 127412547 | intron variant | A/G | snv | 0.63 |
|
Digestive System Diseases; Neoplasms | 0.830 | 0.889 | 9 | 2008 | 2019 | |||||||
|
0.807 | 0.160 | 8 | 127375606 | intron variant | T/C | snv | 0.41 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.730 | 1.000 | 5 | 2010 | 2015 | |||||||
|
0.807 | 0.160 | 8 | 127375606 | intron variant | T/C | snv | 0.41 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.730 | 1.000 | 5 | 2010 | 2015 | |||||||
|
0.925 | 0.080 | 8 | 127098007 | intron variant | A/G | snv | 0.13 |
|
Neoplasms; Male Urogenital Diseases | 0.730 | 1.000 | 5 | 2008 | 2016 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2007 | 2018 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.040 | 1.000 | 4 | 2014 | 2016 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
0.700 | 1.000 | 4 | 2007 | 2018 | ||||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2007 | 2018 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2007 | 2018 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.040 | 1.000 | 4 | 2014 | 2016 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
0.700 | 1.000 | 4 | 2007 | 2018 | ||||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2007 | 2018 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
0.700 | 1.000 | 4 | 2007 | 2018 | ||||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
0.700 | 1.000 | 4 | 2007 | 2018 | ||||||||
|
0.925 | 0.080 | 8 | 127323428 | intron variant | G/A | snv | 0.36 |
|
Neoplasms; Male Urogenital Diseases | 0.730 | 0.750 | 4 | 2008 | 2017 | |||||||
|
0.882 | 0.120 | 8 | 127410882 | intron variant | A/G | snv | 0.52 |
|
Neoplasms; Male Urogenital Diseases | 0.720 | 1.000 | 4 | 2008 | 2014 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
0.030 | 1.000 | 3 | 2014 | 2018 | ||||||||
|
0.925 | 0.080 | 8 | 127098007 | intron variant | A/G | snv | 0.13 |
|
Neoplasms; Male Urogenital Diseases | 0.030 | 1.000 | 3 | 2012 | 2016 |