|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients.
|
28445943 |
2017 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Exonic Splicing Mutations Are More Prevalent than Currently Estimated and Can Be Predicted by Using In Silico Tools.
|
26761715 |
2016 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses.
|
26247049 |
2015 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses.
|
26247049 |
2015 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Performance characteristics of screening strategies for Lynch syndrome in unselected women with newly diagnosed endometrial cancer who have undergone universal germline mutation testing.
|
25081409 |
2014 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
|
24362816 |
2014 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies.
|
21404117 |
2011 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies.
|
21404117 |
2011 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.
|
20020535 |
2010 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
|
20587412 |
2010 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.
|
20682701 |
2010 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germ line MLH1 and MSH2 mutations in Taiwanese Lynch syndrome families: characterization of a founder genomic mutation in the MLH1 gene.
|
19419416 |
2009 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Redundant DNA methylation in colorectal cancers of Lynch-syndrome patients.
|
18618713 |
2008 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A large fraction of unclassified variants of the mismatch repair genes MLH1 and MSH2 is associated with splicing defects.
|
18561205 |
2008 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The effect of genetic background on the function of Saccharomyces cerevisiae mlh1 alleles that correspond to HNPCC missense mutations.
|
17210669 |
2007 |
|
rs63751194
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Novel and recurrent germline alterations in the MLH1 and MSH2 genes identified in hereditary nonpolyposis colorectal cancer patients in Slovakia.
|
16830052 |
2006 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer.
|
15713769 |
2005 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of germ-line MLH1 and MSH2 mutations in Austrian patients with hereditary nonpolyposis colorectal cancer.
|
15926618 |
2005 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC.
|
14699485 |
2004 |
|
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system.
|
11781295 |
2002 |