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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.763 | 0.160 | 8 | 127014615 | intron variant | C/T | snv | 0.37 |
|
Female Urogenital Diseases and Pregnancy Complications | 0.010 | 1.000 | 1 | 2020 | 2020 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Digestive System Diseases; Neoplasms | 0.900 | 0.945 | 55 | 2007 | 2019 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Neoplasms; Male Urogenital Diseases | 0.800 | 0.871 | 31 | 2007 | 2019 | |||||||
|
0.724 | 0.480 | 8 | 127112671 | intron variant | C/A | snv | 0.16 |
|
Neoplasms; Male Urogenital Diseases | 0.800 | 0.955 | 22 | 2007 | 2019 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Digestive System Diseases; Neoplasms | 0.770 | 1.000 | 21 | 2007 | 2019 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Digestive System Diseases; Neoplasms | 0.730 | 1.000 | 17 | 2007 | 2019 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.890 | 0.938 | 16 | 2007 | 2019 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.100 | 0.933 | 15 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 14 | 2007 | 2019 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
0.700 | 1.000 | 14 | 2007 | 2019 | ||||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 14 | 2007 | 2019 | |||||||
|
0.732 | 0.240 | 8 | 127412547 | intron variant | A/G | snv | 0.63 |
|
Digestive System Diseases; Neoplasms | 0.830 | 0.889 | 9 | 2008 | 2019 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Digestive System Diseases; Neoplasms | 0.760 | 0.857 | 7 | 2010 | 2019 | |||||||
|
0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 |
|
Neoplasms | 0.030 | 1.000 | 3 | 2008 | 2019 | |||||||
|
1.000 | 0.080 | 8 | 126999692 | intron variant | T/C | snv | 0.28 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 2 | 2015 | 2019 | |||||||
|
0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2016 | 2019 | |||||||
|
8 | 127322655 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 2 | 2018 | 2019 | |||||||||||
|
0.790 | 0.200 | 8 | 127091692 | non coding transcript exon variant | T/A;C | snv |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
0.827 | 0.160 | 8 | 127088680 | non coding transcript exon variant | A/G | snv | 1.7E-02 |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2017 | 2019 | |||||||
|
0.827 | 0.160 | 8 | 127088680 | non coding transcript exon variant | A/G | snv | 1.7E-02 |
|
Digestive System Diseases; Neoplasms | 0.020 | 1.000 | 2 | 2017 | 2019 | |||||||
|
0.776 | 0.080 | 8 | 127402647 | intron variant | T/C | snv | 0.59 |
|
Digestive System Diseases; Neoplasms | 0.710 | 1.000 | 2 | 2012 | 2019 | |||||||
|
0.807 | 0.240 | 8 | 127081052 | non coding transcript exon variant | C/T | snv | 0.20 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 |