rs63750206
|
|
A |
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 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Integrated analysis of unclassified variants in mismatch repair genes.
|
21239990 |
2011 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Integrated analysis of unclassified variants in mismatch repair genes.
|
21239990 |
2011 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).
|
18383312 |
2008 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis.
|
18337503 |
2008 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis.
|
18337503 |
2008 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).
|
18383312 |
2008 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Analysis of hMLH1 missense mutations in East Asian patients with suspected hereditary nonpolyposis colorectal cancer.
|
18094436 |
2007 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.
|
17312306 |
2007 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.
|
17312306 |
2007 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Analysis of hMLH1 missense mutations in East Asian patients with suspected hereditary nonpolyposis colorectal cancer.
|
18094436 |
2007 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.
|
16083711 |
2005 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1.
|
16083711 |
2005 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Low levels of microsatellite instability characterize MLH1 and MSH2 HNPCC carriers before tumor diagnosis.
|
15563510 |
2005 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Low levels of microsatellite instability characterize MLH1 and MSH2 HNPCC carriers before tumor diagnosis.
|
15563510 |
2005 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genetic characterization of Chinese hereditary non-polyposis colorectal cancer by DHPLC and multiplex PCR.
|
15613555 |
2004 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genetic characterization of Chinese hereditary non-polyposis colorectal cancer by DHPLC and multiplex PCR.
|
15613555 |
2004 |
rs63750206
|
|
A |
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 |
rs63750206
|
|
C |
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 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review.
|
12419761 |
2002 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review.
|
12419761 |
2002 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of human MLH1 and MSH2 missense variants and hybrid human-yeast MLH1 proteins in Saccharomyces cerevisiae.
|
11555625 |
2001 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of human MLH1 and MSH2 missense variants and hybrid human-yeast MLH1 proteins in Saccharomyces cerevisiae.
|
11555625 |
2001 |
rs63750206
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae.
|
9697702 |
1998 |
rs63750206
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae.
|
9697702 |
1998 |