×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
28503822
2018
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia.
28528518
2018
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
28466842
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
28514183
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
27978560
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A 30-Year-Old Man with Three Primary Malignancies: A Case of Constitutional Mismatch Repair Deficiency.
28286799
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Practical guidance for mismatch repair-deficiency testing in endometrial cancer.
27742654
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Lost in translation: returning germline genetic results in genome-scale cancer research.
28454591
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts.
27273229
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma.
28125078
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
28514183
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
In Silico Systems Biology Analysis of Variants of Uncertain Significance in Lynch Syndrome Supports the Prioritization of Functional Molecular Validation.
28765196
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
28874130
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
28152038
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Practical guidance for mismatch repair-deficiency testing in endometrial cancer.
27742654
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
28466842
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria.
28365877
2017
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
27694994
2016
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.
27433846
2016
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312
2016
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
27476653
2016
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
PMS2 monoallelic mutation carriers: the known unknown.
25856668
2016
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers.
26110232
2016
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Germline PMS2 mutation screened by mismatch repair protein immunohistochemistry of colorectal cancer in Japan.
27589204
2016
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.
26895986
2016