|
Carcinogenesis
|
|
0.010 |
GeneticVariation
|
BEFREE |
The mutation of APC (rs137854573, c.C1606T, p.R536X) could result in HB carcinogenesis by activating Wnt signaling.
|
30619485 |
2018 |
|
Hepatoblastoma
|
|
0.010 |
GeneticVariation
|
BEFREE |
The mutation of APC (rs137854573, c.C1606T, p.R536X) could result in HB carcinogenesis by activating Wnt signaling.
|
30619485 |
2018 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
|
26613750 |
2016 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
|
26613750 |
2016 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.
|
20924072 |
2011 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.
|
20924072 |
2011 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.
|
20924072 |
2011 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
A survey of APC mutations in Quebec.
|
21779980 |
2011 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.
|
20685668 |
2010 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.
|
20685668 |
2010 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
|
19793053 |
2009 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history.
|
15951963 |
2005 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.
|
20223039 |
2005 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history.
|
15951963 |
2005 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.
|
20223039 |
2005 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.
|
20223039 |
2005 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutation analysis of the adenomatous polyposis coli (APC) gene in Danish patients with familial adenomatous polyposis (FAP).
|
15108286 |
2004 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutation analysis of the adenomatous polyposis coli (APC) gene in Danish patients with familial adenomatous polyposis (FAP).
|
15108286 |
2004 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
De novo mutations in familial adenomatous polyposis (FAP).
|
12357334 |
2002 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
De novo mutations in familial adenomatous polyposis (FAP).
|
12357334 |
2002 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
De novo mutations in familial adenomatous polyposis (FAP).
|
12357334 |
2002 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis.
|
8990002 |
1997 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis.
|
1324223 |
1992 |
|
Adenomatous Polyposis Coli
|
|
0.700 |
CausalMutation
|
CLINVAR |
Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis.
|
1324223 |
1992 |
|
Polyposis, Adenomatous Intestinal
|
|
0.700 |
CausalMutation
|
CLINVAR |
Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis.
|
1324223 |
1992 |