|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study.
|
27829682 |
2017 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Similar colorectal cancer risk in patients with monoallelic and biallelic mutations in the MYH gene identified in a population with adenomatous polyposis.
|
17949294 |
2007 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
CLINVAR |
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
|
18301448 |
2008 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
CausalMutation
|
CLINVAR |
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
|
18301448 |
2008 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
|
18301448 |
2008 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
CausalMutation
|
CLINVAR |
MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps.
|
15236166 |
2004 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
CLINVAR |
MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps.
|
15236166 |
2004 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps.
|
15236166 |
2004 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
CLINVAR |
MutYH (MYH) and colorectal cancer.
|
16042573 |
2005 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
CausalMutation
|
CLINVAR |
Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis.
|
19279422 |
2009 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
CLINVAR |
Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis.
|
19279422 |
2009 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis.
|
19279422 |
2009 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
CausalMutation
|
CLINVAR |
Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis.
|
16890597 |
2006 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
CLINVAR |
Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis.
|
16890597 |
2006 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis.
|
16890597 |
2006 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
CausalMutation
|
CLINVAR |
Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis.
|
18091433 |
2007 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis.
|
18091433 |
2007 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
|
25452455 |
2015 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
CLINVAR |
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
|
25820570 |
2015 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
CausalMutation
|
CLINVAR |
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
|
25820570 |
2015 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
|
25820570 |
2015 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
GeneticVariation
|
CLINVAR |
First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
|
21195604 |
2011 |
|
Colorectal Adenomatous Polyposis, Autosomal Recessive
|
|
0.800 |
CausalMutation
|
CLINVAR |
First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
|
21195604 |
2011 |
|
Neoplastic Syndromes, Hereditary
|
|
0.700 |
CausalMutation
|
CLINVAR |
First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
|
21195604 |
2011 |