ClinVar
|
Risk
|
rs1057519998(A;A) rs1057519998(C;C) rs1057519998(G;G) |
Alt
|
rs1057519998(A;A) rs1057519998(C;C) rs1057519998(G;G) |
Reference
|
Rs1057519998(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Uterine cervical neoplasms Neoplasm of brain Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Colorectal Neoplasms Neoplasm of breast Adenocarcinoma of lung Glioblastoma Transitional cell carcinoma of the bladder Pancreatic adenocarcinoma |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Uterine cervical neoplasms Neoplasm of brain Ovarian Serous Cystadenocarcinoma Squamous cell carcinoma of the head and neck Hepatocellular carcinoma Colorectal Neoplasms Neoplasm of breast Adenocarcinoma of lung Glioblastoma Transitional cell carcinoma of the bladder Pancreatic adenocarcinoma |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578268A>C; NC_000017.10:g.7578268A>G; NC_000017.10:g.7578268A>T |
CLNSRC |
|
CLNACC |
RCV000419180.1, RCV000420755.1, RCV000422070.1, RCV000424933.1, RCV000428827.1, RCV000430366.1, RCV000431014.1, RCV000436915.1, RCV000437791.1, RCV000439886.1, RCV000440633.1, RCV000419057.1, RCV000423937.1, RCV000424516.1, RCV000425646.1, RCV000426810.1, RCV000433343.1, RCV000433582.1, RCV000436323.1, RCV000441162.1, RCV000441887.1, RCV000442808.1, RCV000421586.1, RCV000422209.1, RCV000426499.1, RCV000427064.1, RCV000431615.1, RCV000431831.1, RCV000434795.1, RCV000436747.1, RCV000442619.1, RCV000443173.1, RCV000443531.1, |