rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer.
|
8993976 |
1997 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
|
9718327 |
1998 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae.
|
9697702 |
1998 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer.
|
10480359 |
1999 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer.
|
10037723 |
1999 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The interaction of DNA mismatch repair proteins with human exonuclease I.
|
11427529 |
2001 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A yeast two-hybrid assay provides a simple way to evaluate the vast majority of hMLH1 germ-line mutations.
|
12810663 |
2003 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.
|
16083711 |
2005 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer.
|
17453009 |
2007 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of human MLH1 variants using yeast and in vitro mismatch repair assays.
|
17510385 |
2007 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The interplay between hMLH1 and hMRE11: role in MMR and the effect of hMLH1 mutations.
|
18373977 |
2008 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.
|
18566915 |
2009 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry.
|
22949379 |
2013 |
rs63751247
|
|
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 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer.
|
28640387 |
2017 |
rs63751247
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Evaluation of MLH1 variants of unclear significance.
|
29520894 |
2018 |