ClinVar
|
Risk
|
rs1057519747(A;A) rs1057519747(C;C) rs1057519747(G;G) |
Alt
|
rs1057519747(A;A) rs1057519747(C;C) rs1057519747(G;G) |
Reference
|
Rs1057519747(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Pancreatic adenocarcinoma Malignant melanoma of skin Acute myeloid leukemia Small cell lung cancer Adrenocortical carcinoma Oesophageal carcinoma Neoplasm of brain Hepatocellular carcinoma Adenocarcinoma of lung Neoplasm of breast Malignant neoplasm of body of uterus Colorectal Neoplasms Adenocarcinoma of stomach Ovarian Serous Cystadenocarcinoma Brainstem glioma Squamous cell carcinoma of the head and neck |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Pancreatic adenocarcinoma Malignant melanoma of skin Acute myeloid leukemia Small cell lung cancer Adrenocortical carcinoma Oesophageal carcinoma Neoplasm of brain Hepatocellular carcinoma Adenocarcinoma of lung Neoplasm of breast Malignant neoplasm of body of uterus Colorectal Neoplasms Adenocarcinoma of stomach Ovarian Serous Cystadenocarcinoma Brainstem glioma Squamous cell carcinoma of the head and neck |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578412A>C; NC_000017.10:g.7578412A>G; NC_000017.10:g.7578412A>T |
CLNSRC |
|
CLNACC |
RCV000418455.1, RCV000419153.1, RCV000421182.1, RCV000421399.1, RCV000424145.1, RCV000426044.1, RCV000429147.1, RCV000429875.1, RCV000430527.1, RCV000432060.1, RCV000432754.1, RCV000437220.1, RCV000441241.1, RCV000441421.1, RCV000442290.1, RCV000445056.1, RCV000419648.1, RCV000420735.1, RCV000420982.1, RCV000421990.1, RCV000426247.1, RCV000428561.1, RCV000430804.1, RCV000430991.1, RCV000432237.1, RCV000436282.1, RCV000437348.1, RCV000437553.1, RCV000438619.1, RCV000438785.1, RCV000439921.1, RCV000445170.1, RCV000419351.1, RCV000420346.1, RCV000421130.1, RCV000425654.1, RCV000425882.1, RCV000430481.1, RCV000430605.1, RCV000431387.1, RCV000435883.1, RCV000437016.1, RCV000437139.1, RCV000441782.1, RCV000442089.1, RCV000443047.1, RCV000443122.1, |