ClinVar
|
Risk
|
rs121913396(C;C) rs121913396(G;G) rs121913396(T;T) |
Alt
|
rs121913396(C;C) rs121913396(G;G) rs121913396(T;T) |
Reference
|
Rs121913396(A;A) |
Significance |
Pathogenic |
Disease |
Malignant melanoma Transitional cell carcinoma of the bladder Malignant neoplasm of body of uterus Malignant melanoma of skin Uterine cervical neoplasms Medulloblastoma Hepatocellular carcinoma Adenocarcinoma of prostate Adenocarcinoma of stomach Pilomatrixoma not provided Endometrial neoplasm |
Variation | info |
---|
Gene |
CTNNB1 |
CLNDBN |
Malignant melanoma Transitional cell carcinoma of the bladder Malignant neoplasm of body of uterus Malignant melanoma of skin Uterine cervical neoplasms Medulloblastoma Hepatocellular carcinoma Adenocarcinoma of prostate Adenocarcinoma of stomach Pilomatrixoma not provided Endometrial neoplasm |
Reversed |
0 |
HGVS |
NC_000003.11:g.41266098A>C; NC_000003.11:g.41266098A>G; NC_000003.11:g.41266098A>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000421005.1, RCV000421851.1, RCV000422917.1, RCV000428408.1, RCV000429284.1, RCV000433870.1, RCV000438648.1, RCV000439506.1, RCV000443906.1, RCV000019140.5, RCV000087199.2, RCV000417687.1, RCV000425010.1, RCV000427454.1, RCV000427896.1, RCV000433199.1, RCV000435333.1, RCV000437703.1, RCV000443060.1, RCV000443883.1, RCV000418872.1, RCV000422753.1, RCV000423474.1, RCV000429141.1, RCV000430242.1, RCV000434746.1, RCV000436415.1, RCV000439390.1, RCV000440497.1, |