ClinVar
|
Risk
|
rs121913403(A;A) rs121913403(G;G) rs121913403(T;T) |
Alt
|
rs121913403(A;A) rs121913403(G;G) rs121913403(T;T) |
Reference
|
Rs121913403(C;C) |
Significance |
Pathogenic |
Disease |
Malignant melanoma Adenocarcinoma of stomach Medulloblastoma Hepatocellular carcinoma Uterine cervical neoplasms Neoplasm of stomach Malignant neoplasm of body of uterus Adenocarcinoma of lung Transitional cell carcinoma of the bladder Adenocarcinoma of prostate Oesophageal carcinoma Neoplasm of ovary Pilomatrixoma not provided Ovarian Neoplasms |
Variation | info |
---|
Gene |
CTNNB1 |
CLNDBN |
Malignant melanoma Adenocarcinoma of stomach Medulloblastoma Hepatocellular carcinoma Uterine cervical neoplasms Neoplasm of stomach Malignant neoplasm of body of uterus Adenocarcinoma of lung Transitional cell carcinoma of the bladder Adenocarcinoma of prostate Oesophageal carcinoma Neoplasm of ovary Pilomatrixoma not provided Ovarian Neoplasms |
Reversed |
0 |
HGVS |
NC_000003.11:g.41266113C>A; NC_000003.11:g.41266113C>G; NC_000003.11:g.41266113C>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000419361.1, RCV000420492.1, RCV000420998.1, RCV000421620.1, RCV000429634.1, RCV000430785.1, RCV000431858.1, RCV000432982.1, RCV000438660.1, RCV000441059.1, RCV000441660.1, RCV000019141.5, RCV000030945.4, RCV000087195.2, RCV000421574.1, RCV000422240.1, RCV000423597.1, RCV000430788.1, RCV000431366.1, RCV000432924.1, RCV000438791.1, RCV000441696.1, RCV000444056.1, RCV000445258.1, RCV000019151.5, RCV000420061.1, RCV000425340.1, RCV000426489.1, RCV000427490.1, RCV000428583.1, RCV000433883.1, RCV000436738.1, RCV000437726.1, RCV000442576.1, RCV000444520.1, RCV000445320.1, |