Geno
|
Mag
|
Summary
|
(G;G)
|
0
|
common in complete genomics
|
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
ClinVar
|
Risk
|
rs28931588(A;A) rs28931588(C;C) rs28931588(T;T) |
Alt
|
rs28931588(A;A) rs28931588(C;C) rs28931588(T;T) |
Reference
|
Rs28931588(G;G) |
Significance |
Pathogenic |
Disease |
Adenocarcinoma of prostate Transitional cell carcinoma of the bladder Medulloblastoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Esophageal Squamous Cell Carcinoma Endometrial neoplasm Uterine cervical neoplasms Malignant melanoma Hepatoblastoma Pilomatrixoma Craniopharyngioma |
Variation | info |
---|
Gene |
CTNNB1 |
CLNDBN |
Adenocarcinoma of prostate Transitional cell carcinoma of the bladder Medulloblastoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach Malignant melanoma of skin Hepatocellular carcinoma Esophageal Squamous Cell Carcinoma Endometrial neoplasm Uterine cervical neoplasms Malignant melanoma Hepatoblastoma Pilomatrixoma Craniopharyngioma |
Reversed |
0 |
HGVS |
NC_000003.11:g.41266097G>A; NC_000003.11:g.41266097G>C; NC_000003.11:g.41266097G>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000421306.1, RCV000423696.1, RCV000425710.1, RCV000431551.1, RCV000432187.1, RCV000432497.1, RCV000438971.1, RCV000441401.1, RCV000444118.1, RCV000444402.1, RCV000419510.1, RCV000421744.1, RCV000422380.1, RCV000429157.1, RCV000429774.1, RCV000430427.1, RCV000437131.1, RCV000439366.1, RCV000440025.1, RCV000019144.3, RCV000128842.6, RCV000418154.1, RCV000419388.1, RCV000420526.1, RCV000426162.1, RCV000426839.1, RCV000430774.1, RCV000437074.1, RCV000438170.1, RCV000441036.1, |
[PMID 19635198] [Correlation of genetic polymorphisms of beta-catenin to hepatitis B virus-related hepatocellular carcinoma].