ClinVar
|
Risk
|
rs1057519975(A;A) rs1057519975(C;C) rs1057519975(G;G) |
Alt
|
rs1057519975(A;A) rs1057519975(C;C) rs1057519975(G;G) |
Reference
|
Rs1057519975(T;T) |
Significance |
Probable-Pathogenic |
Disease |
Colorectal Neoplasms Adenocarcinoma of prostate Squamous cell carcinoma of lung Adenocarcinoma of stomach Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Adrenocortical carcinoma Transitional cell carcinoma of the bladder Neoplasm of breast Pancreatic adenocarcinoma Adenocarcinoma of lung Neoplasm of brain Hepatocellular carcinoma |
Variation | info |
---|
Gene |
TP53 |
CLNDBN |
Colorectal Neoplasms Adenocarcinoma of prostate Squamous cell carcinoma of lung Adenocarcinoma of stomach Oesophageal carcinoma Ovarian Serous Cystadenocarcinoma Adrenocortical carcinoma Transitional cell carcinoma of the bladder Neoplasm of breast Pancreatic adenocarcinoma Adenocarcinoma of lung Neoplasm of brain Hepatocellular carcinoma |
Reversed |
1 |
HGVS |
NC_000017.10:g.7578527A>C; NC_000017.10:g.7578527A>G; NC_000017.10:g.7578527A>T |
CLNSRC |
|
CLNACC |
RCV000418158.1, RCV000420954.1, RCV000422074.1, RCV000423071.1, RCV000428411.1, RCV000429525.1, RCV000432330.1, RCV000433361.1, RCV000437581.1, RCV000438642.1, RCV000439732.1, RCV000444598.1, RCV000445231.1, RCV000418091.1, RCV000422903.1, RCV000423943.1, RCV000425388.1, RCV000426036.1, RCV000430504.1, RCV000432610.1, RCV000433604.1, RCV000434656.1, RCV000440105.1, RCV000441192.1, RCV000444209.1, RCV000444995.1, RCV000420576.1, RCV000422226.1, RCV000424613.1, RCV000426276.1, RCV000426947.1, RCV000430830.1, RCV000431837.1, RCV000432917.1, RCV000437180.1, RCV000438245.1, RCV000443653.1, RCV000444857.1, RCV000444883.1, |