Variant: rs1114167806 

    present in Gene: MSH2
    present in Chromosome: 2
    Position on Chromosome: 47463096
    Alleles of this Variant: ATGA/-;ATGAATGA

rs1114167806 in MSH2 gene and Hereditary Nonpolyposis Colorectal Cancer PMID 10413423 1999 Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer.

PMID 12386821 2002 Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers.

PMID 15042510 2004 MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population.

rs1114167806 in MSH2 gene and Neoplastic Syndromes, Hereditary PMID 10413423 1999 Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer.

PMID 15516845 2004 A636P testing in Ashkenazi Jews.

PMID 28874130 2017 A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.

PMID 26787237 2016 Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.

PMID 15042510 2004 MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population.

PMID 12386821 2002 Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers.