Disease | N. SNPs d | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AFEXOME | AFGENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Bronchogenic Carcinoma
|
1 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.010 | 1.000 | 1 | 1991 | 1991 | ||||
Carcinoma of lung
|
1204 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.100 | 0.900 | 20 | 1998 | 2017 | ||||
Malignant neoplasm of lung
|
1142 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.100 | 0.900 | 20 | 1998 | 2017 | ||||
Primary malignant neoplasm of lung
|
981 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.100 | 0.900 | 20 | 1998 | 2017 | ||||
Breast Carcinoma
|
2793 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.080 | 1.000 | 8 | 2001 | 2016 | ||||
Malignant neoplasm of breast
|
3417 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.080 | 1.000 | 8 | 2001 | 2016 | ||||
Adenocarcinoma of lung (disorder)
|
563 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 1.000 | 3 | 2002 | 2008 | ||||
Malignant Neoplasms
|
1641 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.060 | 1.000 | 6 | 2003 | 2019 | ||||
Primary malignant neoplasm
|
1374 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.050 | 1.000 | 5 | 2003 | 2019 | ||||
Carcinogenesis
|
355 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.020 | 1.000 | 2 | 2003 | 2008 | ||||
Rectal Carcinoma
|
112 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.010 | 1.000 | 1 | 2004 | 2004 | ||||
Malignant neoplasm of prostate
|
1082 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.050 | 1.000 | 5 | 2005 | 2019 | ||||
Prostate carcinoma
|
1168 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.050 | 1.000 | 5 | 2005 | 2019 | ||||
Non-Small Cell Lung Carcinoma
|
712 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.040 | 1.000 | 4 | 2005 | 2014 | ||||
Adenocarcinoma
|
168 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
Squamous cell carcinoma of lung
|
283 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
Gallbladder Carcinoma
|
75 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.040 | 0.500 | 4 | 2007 | 2014 | ||||
Endometrial Carcinoma
|
326 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 3 | 2007 | 2012 | |||||
Malignant neoplasm of endometrium
|
197 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 3 | 2007 | 2012 | |||||
Malignant neoplasm of gallbladder
|
81 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 0.667 | 3 | 2007 | 2014 | ||||
Stage 0 Gallbladder Cancer AJCC v8
|
56 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 0.667 | 3 | 2007 | 2014 | ||||
Stage IIA Gallbladder Cancer AJCC v8
|
56 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 0.667 | 3 | 2007 | 2014 | ||||
Stage IIB Gallbladder Cancer AJCC v8
|
56 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 0.667 | 3 | 2007 | 2014 | ||||
Stage III Gallbladder Cancer AJCC v8
|
56 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 0.667 | 3 | 2007 | 2014 | ||||
Stage IV Gallbladder Cancer AJCC v8
|
56 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 0.030 | 0.667 | 3 | 2007 | 2014 |