ClinVar
|
Risk
|
rs1057519985(C;C) rs1057519985(G;G) rs1057519985(T;T) |
Alt
|
rs1057519985(C;C) rs1057519985(G;G) rs1057519985(T;T) |
Reference
|
Rs1057519985(A;A) |
Significance |
Probable-Pathogenic |
Disease |
Oesophageal carcinoma Acute myeloid leukemia Neoplasm of breast Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Colorectal Neoplasms Squamous cell carcinoma of the head and neck Squamous cell carcinoma of the skin Hepatocellular carcinoma Adenocarcinoma of stomach Neoplasm of brain Adenocarcinoma of lung Malignant melanoma of skin Small cell lung cancer Transitional cell carcinoma of the bladder |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Oesophageal carcinoma Acute myeloid leukemia Neoplasm of breast Pancreatic adenocarcinoma Ovarian Serous Cystadenocarcinoma Colorectal Neoplasms Squamous cell carcinoma of the head and neck Squamous cell carcinoma of the skin Hepatocellular carcinoma Adenocarcinoma of stomach Neoplasm of brain Adenocarcinoma of lung Malignant melanoma of skin Small cell lung cancer Transitional cell carcinoma of the bladder |
Reversed |
1 |
HGVS |
NC_000017.10:g.7577081T>A; NC_000017.10:g.7577081T>C; NC_000017.10:g.7577081T>G |
CLNSRC |
|
CLNACC |
RCV000417903.1, RCV000420631.1, RCV000423140.1, RCV000424403.1, RCV000425922.1, RCV000430027.1, RCV000430739.1, RCV000432539.1, RCV000435554.1, RCV000436172.1, RCV000438282.1, RCV000440264.1, RCV000443104.1, RCV000443133.1, RCV000443946.1, RCV000419110.1, RCV000421308.1, RCV000421511.1, RCV000426176.1, RCV000427234.1, RCV000428935.1, RCV000429960.1, RCV000432174.1, RCV000433559.1, RCV000434654.1, RCV000438516.1, RCV000439628.1, RCV000439864.1, RCV000442747.1, RCV000443562.1, RCV000419358.1, RCV000421331.1, RCV000421888.1, RCV000423414.1, RCV000424971.1, RCV000427672.1, RCV000430190.1, RCV000431576.1, RCV000433092.1, RCV000434375.1, RCV000437905.1, RCV000439537.1, RCV000443287.1, RCV000443500.1, RCV000444095.1, |