ClinVar
|
Risk
|
rs1057519989(A;A) rs1057519989(C;C) rs1057519989(T;T) |
Alt
|
rs1057519989(A;A) rs1057519989(C;C) rs1057519989(T;T) |
Reference
|
Rs1057519989(G;G) |
Significance |
Probable-Pathogenic |
Disease |
Glioblastoma Colorectal Neoplasms Hepatocellular carcinoma Neoplasm of brain Small cell lung cancer Malignant neoplasm of body of uterus Squamous cell carcinoma of lung Uterine Carcinosarcoma Oesophageal carcinoma Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Adenocarcinoma of stomach Hereditary cancer-predisposing syndrome |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Glioblastoma Colorectal Neoplasms Hepatocellular carcinoma Neoplasm of brain Small cell lung cancer Malignant neoplasm of body of uterus Squamous cell carcinoma of lung Uterine Carcinosarcoma Oesophageal carcinoma Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Adenocarcinoma of lung Adenocarcinoma of stomach Hereditary cancer-predisposing syndrome |
Reversed |
1 |
HGVS |
NC_000017.10:g.7577551C>A; NC_000017.10:g.7577551C>G; NC_000017.10:g.7577551C>T |
CLNSRC |
|
CLNACC |
RCV000418385.1, RCV000419449.1, RCV000422508.1, RCV000427774.1, RCV000427875.1, RCV000429067.1, RCV000430162.1, RCV000436692.1, RCV000437360.1, RCV000437805.1, RCV000438569.1, RCV000439724.1, RCV000443459.1, RCV000418001.1, RCV000419267.1, RCV000420351.1, RCV000424520.1, RCV000425133.1, RCV000425485.1, RCV000430145.1, RCV000431028.1, RCV000432729.1, RCV000435229.1, RCV000437599.1, RCV000438254.1, RCV000443153.1, RCV000418805.1, RCV000421362.1, RCV000423748.1, RCV000425382.1, RCV000426057.1, RCV000426513.1, RCV000432031.1, RCV000433704.1, RCV000434459.1, RCV000436060.1, RCV000441006.1, RCV000442909.1, RCV000443654.1, RCV000492366.1, |