Varaico: Literature-Extracted Genetic Variants

Gene:MSH6
Variant:p.R1024W
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MSH6

NM_000179.3:p.R1024W

Associated Papers

Genome-wide analysis of somatic noncoding mutation patterns and mitochondrial heteroplasmic shift in type B1 and B2 thymomas.

Fujikura K et al.

The Journal of Pathology, 2026

41344988 (PubMed )
Supplement: PATH-268-135-s001.xlsx › Table_S3

A primary luminal/HER2 negative breast cancer patient with mismatch repair deficiency.

Yang X et al.

Cell Death Discovery, 2023

Genetic alterations and their therapeutic implications in epithelial ovarian cancer.

Lapke N et al.

Bmc Cancer, 2021

33947352 (PubMed )
Supplement: 12885_2021_8233_MOESM5_ESM.xlsx › Additional_file_5

Longitudinal analysis of treatment-induced genomic alterations in gliomas.

Erson-Omay EZ et al.

Genome Medicine, 2017

28153049 (PubMed )
Supplement: 13073_2017_401_MOESM3_ESM.xlsx › AllMutations_Clonality

CoDP: predicting the impact of unclassified genetic variants in MSH6 by the combination of different properties of the protein.

Terui H et al.

Journal of Biomedical Science, 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."