rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry.
|
25117503 |
2014 |
rs28929483
|
|
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 |
rs28929483
|
|
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 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
High-resolution melting analyses for gene scanning of APC, MLH1, MSH2, and MSH6 associated with hereditary colorectal cancer.
|
22283331 |
2012 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.
|
22102614 |
2012 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Characterization of MSH2 variants by endogenous gene modification in mouse embryonic stem cells.
|
21309037 |
2011 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics.
|
19267393 |
2009 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of HNPCC-related missense mutations in MSH2.
|
18822302 |
2008 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional characterization of pathogenic human MSH2 missense mutations in Saccharomyces cerevisiae.
|
17720936 |
2007 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.
|
16616355 |
2006 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer.
|
16116158 |
2005 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions.
|
12124176 |
2002 |
rs28929483
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
|
8261515 |
1993 |