Varaico: Literature-Extracted Genetic Variants

Gene:MSH6
Variant:p.E207*
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MSH6

NM_000179.3:p.E207*

Associated Papers

Comprehensive genomic profiling of Chinese lung cancer characterizes germline-somatic mutation interactions influencing cancer risk.

Zhou N et al.

Journal of Translational Medicine, 2025

Prevalence of the cancer-associated germline variants in Russian adults and long-living individuals: using the ACMG recommendations and computational interpreters for pathogenicity assessment.

Gusakova M et al.

Frontiers in Oncology, 2024

39301547 (PubMed )
Supplement: DataSheet1.zip › Supplementary_Table_3.XLSX › all_group_1

An MSH6 germline pathogenic variant p.Gly162Ter associated with Lynch syndrome.

Vostrukhina OA et al.

Human Genome Variation, 2022

Prevalence and spectrum of DNA mismatch repair gene variation in the general Chinese population.

Zhang L et al.

Journal of Medical Genetics, 2022

34172528 (PubMed )
Supplement: jmedgenet-2021-107886supp006.xlsx › MSH2

MSH6, Past and Present and Muir-Torre Syndrome-Connecting the Dots.

Mahalingam M

The American Journal of Dermatopathology, 2017

Molecular and clinical characteristics of MSH6 germline variants detected in colorectal cancer patients.

Terui H et al.

Oncology Reports, 2013

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."