rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.
|
20020535 |
2010 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer.
|
25003300 |
2014 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A human compound heterozygote for two MLH1 missense mutations.
|
9326924 |
1997 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.
|
23535968 |
2013 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.
|
22753075 |
2012 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer.
|
10375096 |
1999 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.
|
23408351 |
2013 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Four new mutations in the DNA mismatch repair gene MLH1 in colorectal cancers with microsatellite instability. Mutations in brief no. 157. Online.
|
10627141 |
1998 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).
|
24310308 |
2014 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing.
|
11839723 |
2002 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
|
25452455 |
2015 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer.
|
8993976 |
1997 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Lynch Syndrome: A Primer for Urologists and Panel Recommendations.
|
25711197 |
2015 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms?
|
11726306 |
2001 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Missense mutations in hMLH1 associated with colorectal cancer.
|
10598809 |
1999 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
|
25070057 |
2014 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.
|
8571956 |
1996 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Practice parameters for the identification and testing of patients at risk for dominantly inherited colorectal cancer--supporting documentation.
|
11598466 |
2001 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.
|
9311737 |
1997 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer.
|
9559627 |
1998 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
|
25645574 |
2015 |
rs63750710
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer.
|
10413423 |
1999 |