rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.
|
22102614 |
2012 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden.
|
14961575 |
2004 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.
|
15483016 |
2004 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?
|
12522549 |
2003 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
MSH6 germline mutations are rare in colorectal cancer families.
|
14520694 |
2003 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation.
|
11807791 |
2002 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant.
|
11709755 |
2002 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Germline and somatic mutations in hMSH6 and hMSH3 in gastrointestinal cancers of the microsatellite mutator phenotype.
|
11470537 |
2001 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium?
|
11153917 |
2000 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer.
|
10699937 |
2000 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer.
|
10413423 |
1999 |
rs63750304
|
|
Colorectal Carcinoma
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Germ-line msh6 mutations in colorectal cancer families.
|
10537275 |
1999 |