ClinVar
|
Risk
|
rs786203436(A;A) rs786203436(C;C) rs786203436(G;G) |
Alt
|
rs786203436(A;A) rs786203436(C;C) rs786203436(G;G) |
Reference
|
Rs786203436(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Hereditary cancer-predisposing syndrome Small cell lung cancer Uterine Carcinosarcoma Hepatocellular carcinoma Adenocarcinoma of lung Malignant melanoma of skin Neoplasm of breast Colorectal Neoplasms Neoplasm of brain Squamous cell carcinoma of the head and neck Oesophageal carcinoma Brainstem glioma Pancreatic adenocarcinoma Squamous cell carcinoma of lung Ovarian Serous Cystadenocarcinoma |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Hereditary cancer-predisposing syndrome Small cell lung cancer Uterine Carcinosarcoma Hepatocellular carcinoma Adenocarcinoma of lung Malignant melanoma of skin Neoplasm of breast Colorectal Neoplasms Neoplasm of brain Squamous cell carcinoma of the head and neck Oesophageal carcinoma Brainstem glioma Pancreatic adenocarcinoma Squamous cell carcinoma of lung Ovarian Serous Cystadenocarcinoma |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578443A>C; NC_000017.10:g.7578443A>G; NC_000017.10:g.7578443A>T |
CLNSRC |
UniProtKB (protein) |
CLNACC |
RCV000166739.1, RCV000417885.1, RCV000420162.1, RCV000420721.1, RCV000424608.1, RCV000425235.1, RCV000426124.1, RCV000430982.1, RCV000432709.1, RCV000433509.1, RCV000434903.1, RCV000435516.1, RCV000441262.1, RCV000443587.1, RCV000444147.1, RCV000417511.1, RCV000418221.1, RCV000418859.1, RCV000423239.1, RCV000423893.1, RCV000425645.1, RCV000428451.1, RCV000431265.1, RCV000434193.1, RCV000435900.1, RCV000436639.1, RCV000438678.1, RCV000440924.1, RCV000441609.1, RCV000421406.1, RCV000422095.1, RCV000424159.1, RCV000426404.1, RCV000427021.1, RCV000428833.1, RCV000431660.1, RCV000434430.1, RCV000437297.1, RCV000439053.1, RCV000439742.1, RCV000443298.1, RCV000443877.1, RCV000444003.1, |