ClinVar
|
Risk
|
rs1057520000(A;A) rs1057520000(G;G) |
Alt
|
rs1057520000(A;A) rs1057520000(G;G) |
Reference
|
Rs1057520000(C;C) |
Significance |
Probable-Pathogenic |
Disease |
Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Colorectal Neoplasms Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Multiple myeloma Neoplasm of brain Malignant melanoma of skin Malignant neoplasm of body of uterus Uterine Carcinosarcoma Squamous cell carcinoma of lung Adenocarcinoma of lung Oesophageal carcinoma Adenoid cystic carcinoma Neoplasm of breast |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Colorectal Neoplasms Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Multiple myeloma Neoplasm of brain Malignant melanoma of skin Malignant neoplasm of body of uterus Uterine Carcinosarcoma Squamous cell carcinoma of lung Adenocarcinoma of lung Oesophageal carcinoma Adenoid cystic carcinoma Neoplasm of breast |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578478G>C; NC_000017.10:g.7578478G>T |
CLNSRC |
|
CLNACC |
RCV000418846.1, RCV000419325.1, RCV000419958.1, RCV000421526.1, RCV000423715.1, RCV000424514.1, RCV000425600.1, RCV000430235.1, RCV000431352.1, RCV000434196.1, RCV000435439.1, RCV000435893.1, RCV000436541.1, RCV000439174.1, RCV000440477.1, RCV000441608.1, RCV000443101.1, RCV000420222.1, RCV000421293.1, RCV000422381.1, RCV000423439.1, RCV000426285.1, RCV000427300.1, RCV000428053.1, RCV000428730.1, RCV000432614.1, RCV000433715.1, RCV000438265.1, RCV000438983.1, RCV000440037.1, RCV000440518.1, RCV000442618.1, RCV000443403.1, RCV000444401.1, |