ClinVar
|
Risk
|
rs121913400(A;A) rs121913400(G;G) rs121913400(T;T) |
Alt
|
rs121913400(A;A) rs121913400(G;G) rs121913400(T;T) |
Reference
|
Rs121913400(C;C) |
Significance |
Other |
Disease |
Carcinoma of colon Pilomatrixoma Adenocarcinoma of prostate Oesophageal carcinoma Pancreatic adenocarcinoma Hepatocellular carcinoma Adenocarcinoma of stomach Malignant melanoma of skin Medulloblastoma Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Endometrial neoplasm Colorectal Neoplasms Adenocarcinoma of lung Parathyroid gland neoplasm Ovarian Neoplasms Neoplasm of brain |
Variation | info |
---|
Gene |
CTNNB1 |
CLNDBN |
Carcinoma of colon Pilomatrixoma Adenocarcinoma of prostate Oesophageal carcinoma Pancreatic adenocarcinoma Hepatocellular carcinoma Adenocarcinoma of stomach Malignant melanoma of skin Medulloblastoma Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Endometrial neoplasm Colorectal Neoplasms Adenocarcinoma of lung Parathyroid gland neoplasm Ovarian Neoplasms Neoplasm of brain |
Reversed |
0 |
HGVS |
NC_000003.11:g.41266101C>A; NC_000003.11:g.41266101C>G; NC_000003.11:g.41266101C>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000019138.5, RCV000019139.5, RCV000418289.1, RCV000423917.1, RCV000424968.1, RCV000426112.1, RCV000430278.1, RCV000434171.1, RCV000435233.1, RCV000435972.1, RCV000437025.1, RCV000443472.1, RCV000443834.1, RCV000444481.1, RCV000419399.1, RCV000420513.1, RCV000421237.1, RCV000421624.1, RCV000425323.1, RCV000429684.1, RCV000430769.1, RCV000431875.1, RCV000432570.1, RCV000432807.1, RCV000438635.1, RCV000441027.1, RCV000441671.1, RCV000444407.1, RCV000019147.5, RCV000019148.6, RCV000418596.1, RCV000420986.1, RCV000421635.1, RCV000423964.1, RCV000428161.1, RCV000434049.1, RCV000437352.1, RCV000438845.1, RCV000439964.1, RCV000443180.1, |