×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
Systematic study on genetic and epimutational profile of a cohort of Amsterdam criteria-defined Lynch Syndrome in Singapore.
24710284
2014
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
28449805
2017
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Molecular screening in Sicilian families with hereditary non-poliposis colorectal cancer (H.N.P.C.C.) syndrome: identification of a novel mutation in MSH2 gene.
25200962
2014
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
RNA-based mutation screening in hereditary nonpolyposis colorectal cancer.
8808596
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions.
22949387
2013
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
Biomarker
group
CLINGEN
Cancer risks for MLH1 and MSH2 mutation carriers.
23255516
2013
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.
9311737
1997
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
LHGDN
MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population.
15042510
2004
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
HNPCC: six new pathogenic mutations.
15217520
2004
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families.
21598002
2011
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
Patient vs. physician as the target of educational outreach about screening for an inherited susceptibility to colorectal cancer.
12537652
2002
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.
9222765
1997
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients.
11772966
2002
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
The InSiGHT database: utilizing 100 years of insights into Lynch syndrome.
23443670
2013
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
Biomarker
group
CTD_human
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.
22102614
2012
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
LHGDN
Clinical features and hMSH2/hMLH1 germ-line mutations in Chinese patients with hereditary nonpolyposis colorectal cancer.
18713544
2008
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers.
24244552
2013
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Predominant germ-line mutation of the hMSH2 gene in Japanese hereditary non-polyposis colorectal cancer kindreds.
10404063
1999
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
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
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.
8574961
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Germ line mutations of hMSH2 and hMLH1 genes in Japanese families with hereditary nonpolyposis colorectal cancer (HNPCC): usefulness of DNA analysis for screening and diagnosis of HNPCC patients.
8581513
1995
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
LHGDN
New founding mutation in MSH2 associated with hereditary nonpolyposis colorectal cancer syndrome on the Island of Tenerife.
16500024
2006
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Prognostic impact of mismatch repair genes germline defects in colorectal cancer patients: are all mutations equal?
26485756
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
8261515
1993
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
21642682
2011